145.ÌýHemati, M.; Wang, D.-S.; Tedder, M.-L.; Zhang, X. P.Ìý“Controlling a Difficult Radical Sequence Enables Asymmetric β-Lactam Synthesis.â€�ÌýChemRxivÌý2026, DOI: 10.26434/chemrxiv.15004019/v1. []

A chemistry diagram

144.ÌýXu, P.; Wang, D.-S.; Zhu, Z.-Y.; Zhang, X. P.Ìý“Enantioselective Radical Dearomative Conjugate Amination Enabled by Co(II)-Based Metalloradical Catalysis.â€�ÌýNat. Catal.Ìý2025, 8, 1051–1061. []

A chemistry diagram

143.ÌýWang, D.-S.; Zhang, X. P.ÌýCobalt-Catalyzed Asymmetric Radical Reactions.ÌýInÌýCatalytic Asymmetric Radical Reactions,ÌýLiu, X.-Y.; Liu, G.ÌýEds.;Ìý2025; ppÌý23–76. []

A chemistry diagram

142.ÌýLee, W.-C. C.; Wang, D.-S.; Deb, A.; Zhu, Y.; Zhang, X. P. “Asymmetric C–H Amination via Fe(III)-Metalloradical Catalysis Featuring α-Fe(IV)-Aminyl Radicals as Key Intermediatesâ€�ÌýJ. Am. Chem. Soc.Ìý2025, 147, 24001–24013. []

TOC-142

141.ÌýZhu, Y.-L.; Lee, W.-C. C.; Zhang, X. P. “Catalytic Metalloradical System for Radical 1,6-C(sp3)–H Amination with Concurrent Control of Site-, Chemo-, and Enantio-selectivityâ€�ÌýJ. Am. Chem. Soc.Ìý2025, 147, 15755–15766. []

A chemistry diagram

140.ÌýLee, W.-C. C.; Zhang, X. P. “Metalloradical Catalysis: General Approach for Controlling Reactivity and Selectivity of Homolytic Radical Reactionsâ€�ÌýAngew. Chem. Int. Ed.Ìý2024,Ìý63, e202320243. []

A chemistry diagram

139.ÌýLee, W.-C. C.; Zhang, X. P. “Asymmetric Radical Aziridination of Alkenesâ€�ÌýTrends Chem.Ìý2024,Ìý6,Ìý95–96. [][]

A chemistry diagram

138.ÌýXu, H.; Wang, D.-S.; Zhu, Z.-Y.; Deb, A.; Zhang, X. P. “New Mode of Asymmetric Induction for Enantioselective RadicalÌýN-Heterobicyclization via Kinetically Stable Chiral Radical Centerâ€�ÌýChemÌý2024,Ìý10,Ìý283–298. []

A chemistry diagram

137.ÌýWang, D.-S.; Zhang, X. P. Oxidation: C─N Bond Formation by Oxidation (Aziridines). In Comprehensive Chirality, Second ed.; Cossy, J. Ed.; Elsevier,Ìý2024; pp 158–179. []

A chemistry diagram

136.ÌýLee, W.-C. C.; Zhang, X. P. “Iron(III) Porphyrin Complexes as Metalloradical Catalystsâ€�ÌýNat. Chem.Ìý2023,Ìý15,Ìý1499–1500. []

A chemistry diagram

135.ÌýLee, W.-C. C.; Wang, D.-S.; Zhu, Y.-L.; Zhang, X. P. “Iron(III)-Based Metalloradical Catalysis for Asymmetric Cyclopropanation via a Stepwise Radical Mechanismâ€�ÌýNat. Chem.Ìý2023,Ìý15,Ìý1569–1580. [] []

A chemistry diagram

134.ÌýLee, W.-C. C.;†ÌýWang, J.-Y.;†ÌýZhu, Y.-L.; Zhang, X. P. “Asymmetric Radical Bicyclization for Stereoselective Construction of Tricyclic Chromanones and Chromanes with Fused Cyclopropanesâ€�ÌýJ. Am. Chem. Soc.Ìý2023,Ìý145,Ìý11622–11632. [] [] []

A chemistry diagram

133.ÌýXu, P.; Xie, J.-J.; Wang, D.-S.; Zhang, X. P. “Metalloradical Approach for Concurrent Control in Intermolecular Radical Allylic C−H Aminationâ€�ÌýNat. Chem.Ìý2023,Ìý15,Ìý498–507. []

A chemistry diagram

132.ÌýNovaes, L. F. T.; Wang, Y.; Liu, J.-J.; Riart-Ferrer, X.; Lee, W.-C. C.; Fu, N.-K.; Zhang, X. P.; Lin, S. “Electrochemical Diazidation of Alkenes Catalyzed by Manganese Porphyrin Complexes with Second-Sphere Hydrogen-Bond Donorsâ€�ÌýACS Catal.Ìý2022,Ìý12,Ìý14106–14112. []

A chemistry diagram

131.ÌýLang, K.; Hu, Y.; Lee, W.-C. C.; Zhang, X. P. “Combined Radical and Ionic Approach for The Enantioselective Synthesis ofÌýβ-Functionalized Amines from Alcoholsâ€�ÌýNat. Synth.Ìý2022,Ìý1,Ìý548–557. [] [] []

A chemistry diagram

130.ÌýÌýLee, W.-C. C.; Zhang, X. P. “Asymmetric Radical Cyclopropanation of Alkenesâ€�ÌýTrends Chem.Ìý2022,Ìý4,Ìý850–851. []

A chemistry diagram

129.ÌýÌýKe, J.; Lee, W.-C. C.; Wang, X.-X.; Wang, Y.; Wen, X.; Zhang, X. P. “Metalloradical Activation of In Situ-GeneratedÌýαÌý-Alkynyldiazomethanes for Asymmetric Radical Cyclopropanation of Alkenesâ€�ÌýJ. Am. Chem. Soc.Ìý2022,Ìý144, 2368–2378. []

A chemistry diagram

128.ÌýÌýWang, X.-X.; Zhang, X. P. “Catalytic Radical Approach for Selective Carbene Transfers via Cobalt(II)-Based Metalloradical Catalysisâ€� InÌýTransition Metal-Catalyzed Carbene TransformationsÌý2022, 25-66. []

A chemistry diagram

127.ÌýÌýWang, J.-Y.; Xie, J.-J.; Lee, W.-C. C.; Wang, D.-S.; Zhang, X. P. “Radical Differentiation of Two Ester Groups in Unsymmetrical Diazomalonates for Highly Asymmetric Olefin Cyclopropanationâ€�ÌýChem Catal.Ìý2022,Ìý2, 330–344. [] [] []

A chemistry diagram

126.ÌýÌýZhang, W.-J.; Nafady, A.; Shan, C.; Wojtas, L.; Chen, Y.-S.; Cheng, Q.-G.; Zhang, X. P.; Ma, S.-Q. “Functional Porphyrinic Metal-Organic Framework as a New Class of Heterogeneous Halogen Bond Donor Catalystâ€�ÌýAngew. Chem. Int. Ed.Ìý2021,Ìý60, 24312–24317. []

A chemistry diagram

125.ÌýÌýXie, J.-J.; Xu, P.; Zhu, Y.-L.; Wang, J.-Y.; Lee, W.-C. C.; Zhang, X. P. “New Catalytic Radical Process Involving 1,4-Hydrogen Atom Abstraction: Asymmetric Construction of Cyclobutanonesâ€�ÌýJ. Am. Chem. Soc.Ìý2021,Ìý143, 11670-11678. []

A chemistry diagram

124.ÌýÌýWang, X.-X.; Ke, J.; Zhu, Y.-L.; Deb, A.; Xu, Y.-J.; Zhang, X. P. “Asymmetric Radical Process for General Synthesis of Chiral Heteroaryl Cyclopropanesâ€�ÌýJ. Am. Chem. Soc.Ìý2021,Ìý143, 11121-11129. []

A chemistry diagram

123.ÌýÌýZhang, C.-Z.; Wang, D.-S.; Lee, W.-C. C.; McKillop, A. M.; Zhang, X. P. “Controlling Enantioselectivity and Diastereoselectivity in Radical Cascade Cyclization for Construction of Bicyclic Structuresâ€�ÌýJ. Am. Chem. Soc.Ìý2021,Ìý143, 11130-11140. []

A chemistry diagram

122.ÌýÌýLee, W.-C. C. “Metalloradical Catalysis: A Radically Different Approach for Molecular Constructionâ€�ÌýChemÌý2021,Ìý7, 1402-1404. []

A chemistry diagram

121.ÌýÌýLee, W.-C. C.; Wang, D.-S.; Zhang, C.-Z.; Xie, J.-J.; Li, B.; Zhang, X. P. “Asymmetric Radical Cyclopropanation of Dehydroaminocarboxylates: Stereoselective Synthesis of CyclopropylÌýα-Amino Acidsâ€�ÌýChemÌý2021,Ìý7, 1588-1601. []

A chemistry diagram

120.ÌýÌýMagnuson, Z. L.; Cheng, Q.-G.; Zhang, W.-J.; Chen, Y.-S.; Wojtas, L.; Nafady, A.; Al-Enizi, A. M.; Larsen, R. W.; Zhang, X. P.; Ma, S.-Q. “Two Manganese Metalloporphyrin Frameworks Constructed from a Custom-Designed Porphyrin Ligand Exhibiting Selective Uptake of CO2Ìýover CH4Ìýand Catalytic Activity for CO2ÌýFixationâ€�ÌýCryst. Growth Des.Ìý2021,Ìý21, 2786–2792. []

A chemistry diagram

119.ÌýÌýRiart-Ferrer, X.; Sang, P.; Tao, J.-R.; Xu, H.; Jin, L.-M.; Lu, H.-J.; Cui, X.; Wojtas, L.; Zhang, X. P. “Metalloradical Activation of Carbonyl Azides for Enantioselective Radical Aziridinationâ€�ÌýChemÌý2021,Ìý7, 1120–1134. []

A chemistry diagram

118.ÌýÌýLang, K.; Li, C.-Q.; Kim, I.; Zhang, X. P. “Enantioconvergent Amination of Racemic Tertiary C-H Bondsâ€�ÌýJ. Am. Chem. Soc.Ìý2020,Ìý142, 20902–20911. []

A chemistry diagram

117.ÌýÌýJin, L.-M.; Xu, P.; Xie, J.-J.; Zhang, X. P. “Enantioselective Intermolecular Radical C−H Aminationâ€�ÌýJ. Am. Chem. Soc.Ìý2020,Ìý142, 20828–20836. []

A chemistry diagram

116.ÌýÌýHu, Y.; Lang, K.; Li, C.-Q.; Gill, J. B.; Kim, I.; Lu, H.-J.; Fields, K. B.; Marshall, M. K.; Cheng, Q.-G.; Cui, X.; Wojtas, L.; Zhang, X. P. “Enantioselective Radical Construction of 5-Membered Cyclic Sulfonamides by Metalloradical C−H Aminationâ€�ÌýJ. Am. Chem. Soc.Ìý2019,Ìý141, 18160-18169. []

A chemistry diagram

115.ÌýÌýLang, K.; Torker, S.; Wojtas, L.; Zhang, X. P. “Asymmetric Induction and Enantiodivergence in Catalytic Radical C–H Amination via Enantiodifferentiative H-Atom Abstraction and Stereoretentive Radical Substitutionâ€�ÌýJ. Am. Chem. Soc.Ìý2019,Ìý141, 12388–12396. []

A chemistry diagram

114.ÌýÌýHu, Y.; Lang, K.; Tao, J.-R.; Marshall, M. K.; Cheng, Q.-G.; Cui, X.; Wojtas, L.; Zhang, X. P. “Next-Generation D2-Symmetric Chiral Porphyrins for Cobalt(II)-Based Metalloradical Catalysis: Catalyst Engineering by Distal Bridgingâ€�ÌýAngew. Chem. Int. Ed.Ìý2019,Ìý58, 2670–2674. []

A chemistry diagram

113.ÌýÌýLi, C.-Q.; Lang, K.; Lu, H,-J.; Hu, Y.; Cui, X.; Wojtas, L.; Zhang, X. P. “Catalytic Radical Process for Enantioselective Amination of C(sp3)-H Bondsâ€�ÌýAngew. Chem. Int. Ed.Ìý2018,Ìý57, 16837–16841. []

A chemistry diagram

112.ÌýÌýWen, X.; Wang, Y.; Zhang, X. P. “Enantioselective Radical Process for Synthesis of Chiral Indolines by Metalloradical Alkylation of Diverse C(sp3)-H Bondsâ€�ÌýChem. Sci.Ìý2018,Ìý9, 5082–5086. []

A chemistry diagram

111.ÌýÌýWang, Y.; Wen, X.; Cui, X.; Zhang, X. P. “Enantioselective Radical Cyclization for Construction of 5-Membered Ring Structures by Metalloradical C-H Alkylationâ€�ÌýJ. Am. Chem. Soc.Ìý2018,Ìý140, 4792–4796. []

A chemistry diagram

110.ÌýÌýWang, Y.; Zhang, X. P. “[Co(3,5-Di-t-Bu-QingPhyrin)]â€�Ìýe-EROS, John Wiley & Sons,Ìý2018;ÌýDOI: 10.1002/047084289X.rn02204. []

A chemistry diagram

109.ÌýÌýWang, Y.; Zhang, X. P. “[Co(3,5-Di-t-Bu-Xu(2′-Naph)Phyrin)]â€�Ìýe-EROS, John Wiley & Sons,Ìý2018;ÌýDOI: 10.1002/047084289X.rn02203. []

A chemistry diagram

108.ÌýÌýWang, Y.; Zhang, X. P. “[Co(3,5-Di-t-Bu-ChenPhyrin)]â€�Ìýe-EROS, John Wiley & Sons,Ìý2018;ÌýDOI: 10.1002/047084289X.rn02202. []

A chemistry diagram

107.ÌýÌýWang, Y.; Zhang, X. P. “[Co(3,5-Di-t-Bu-IbuPhyrin)]â€�Ìýe-EROS, John Wiley & Sons,Ìý2018;ÌýDOI: 10.1002/047084289X.rn02201. []

A chemistry diagram

106.ÌýÌýWang, Y.; Zhang, X. P. “[Co(2,6-DiMeO-ZhuPhyrin)]â€�Ìýe-EROS, John Wiley & Sons,Ìý2018;ÌýDOI: 10.1002/047084289X.rn02200. []

A chemistry diagram

105.ÌýÌýJiang, H.-L.; Lang, K.; Lu, H.-J.; Wojtas, L.; Zhang, X. P. “Asymmetric Radical Bicyclization of Allyl Azidoformates via Cobalt(II)-Based Metalloradical Catalysisâ€�ÌýJ. Am. Chem. Soc.Ìý2017,Ìý139, 9164–9167. []

A chemistry diagram

104.ÌýÌýXu, X.; Wang, Y.; Cui, X.; Wojtas, L.; Zhang, X. P. “Metalloradical Activation ofÌýα-Formyldiazoacetates for Catalytic Asymmetric Radical Cyclopropanation of Alkenesâ€�ÌýChem. Sci.Ìý2017,Ìý8, 4347–4351. []

A chemistry diagram

103.ÌýÌýWang, Y.; Wen, X.; Cui, X.; Wojtas, L.; Zhang, X. P. “Asymmetric Radical Cyclopropanation of Alkenes with In Situ-Generated Donor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysisâ€�ÌýJ. Am. Chem. Soc.Ìý2017,Ìý139, 1049–1052. []

A chemistry diagram

102.ÌýÌýPegis, M. L.; McKeown, B. A.; Kumar, N.; Lang, K.; Wasylenko, D. J.; Zhang, X. P.; Raugei, S.; Mayer, J. M. “Homogenous Electrocatalytic Oxygen Reduction Rates Correlate with Reaction Overpotential in Acidic Organic Solutionsâ€�ÌýACS Cent. Sci.Ìý2016,Ìý2, 850–856. []

A chemistry diagram

101.ÌýÌýJiang, H.-L.; Lang, K.; Lu, H.-J.; Wojtas, L.; Zhang, X. P. “Intramolecular Radical Aziridination of Allylic Sulfamoyl Azides via Co(II)-Based Metalloradical Catalysis: Effective Construction of Strained heterobicyclic Structuresâ€�ÌýAngew. Chem. Int. Ed.Ìý2016,Ìý55, 11604–11608. []

A chemistry diagram

100.ÌýÌýLu, H.-J.; Lang, K.; Jiang, H.-L.; Wojtas, L.; Zhang, X. P. “Intramolecular 1,5-C(sp3)–H Radical Amination via Co(II)-Based Metalloradical Catalysis for Five-Membered Cyclic Sulfamidesâ€�ÌýChem. Sci.Ìý2016,Ìý7, 6934–6939. []

A chemistry diagram

99.ÌýÌýLiu, Q.-J.; Wang, L.-J.; Kang, Q.-K.; Zhang, X. P.; Tang, Y. “Cy-SaBOX/Copper(II)-Catalyzed Highly Diastereo- and Enantioselective Synthesis of Bicyclic N,O Acetalsâ€�ÌýAngew. Chem. Int. Ed.Ìý2016,Ìý55, 9220–9223. []

A chemistry diagram

98.ÌýÌýCui, X.; Zhang, X. P. “C–C Bond Formation Using Carbenesâ€� InÌýScience of Synthesis: Catalytic Transformations via C–H ActivationÌýseries; eds. Yu, J. -Q.; Thieme,Ìý2016, Vol. 2, pp. 63–94. []

A chemistry diagram

97.ÌýÌýLiu, Q.-J.; Yan, W.-G.; Wang, L.-J.; Zhang, X. P.; Tang, Y. “One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazolesâ€�ÌýOrg. Lett.Ìý2015,Ìý17, 4014–4017. []

A chemistry diagram

96.ÌýÌýGoswami, M.; Lyaskovskyy, V.; Domingos, S. R.; Buma, W. J.; Woutersen, S.; Troeppner, O.; Ivanovic-Burmazovic, I.; Lu, H.-J.; Cui, X.; Zhang, X. P.; Reijerse, E. J.; DeBeer S.; van Schooneveld, M. M.; Pfaff, F.; Ray, K.; de Bruin, B. “Characterization of Porphyrin-Co(III)-‘Nitrene Radical’ Species Relevant in Catalytic Nitrene Transfer Reactionsâ€�ÌýJ. Am. Chem. Soc.Ìý2015,Ìý137, 5468–5479. []

A chemistry diagram

95.ÌýÌýSubbarayan, V.; Jin, L.-M., Cui, X.; Zhang, X. P. “Room Temperature Activation of Aryloxysulfonyl Azides by [Co(II)(TPP)] for Selective Radical Aziridination of Alkenes via Metalloradical Catalysisâ€�ÌýTetrahedron Lett.Ìý2015,Ìý56, 3431–3434. []

A chemistry diagram

94.ÌýÌýCui, X.; Xu, X.; Jin, L.-M.; Wojtas, L.; Zhang, X. P. “Stereoselective Radical C–H Alkylation with Acceptor/Acceptor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysisâ€�ÌýChem. Sci.Ìý2015.Ìý6, 1219–1224. []

A chemistry diagram

93.ÌýÌýJin, C.-Y., Decker, A. M.; Huang, X.-P.; Gilmour, B. P.; Blough, B. E.; Roth, B. L.; Hu, Y.; Gill, J. B.; Zhang, X. P. “Synthesis, Pharmacological Characterization, and Structure-Activity Relationship Studies of Small Molecular Agonists for the Orphan GPR88â€�ÌýACS Chem. Neurosci.Ìý2014,Ìý5, 576–587. []

A chemistry diagram

92.ÌýÌýLu, H.-J.; Li, C.-Q.; Jiang, H.-L.; Lizardi, C. L.; Zhang, X. P. “Chemoselective Amination of Propargylic C(sp3)−H Bonds via Co(II)-Based Metalloradical Catalysisâ€�ÌýAngew. Chem. Int. Ed.Ìý2014,Ìý53, 7028–7032. []

A chemistry diagram

91.ÌýÌýTao, J.-R.; Jin, L.-M.; Zhang, X. P. “Synthesis of ChiralÌýN-Phosphoryl Aziridines through Enantioselective Aziridination of Alkenes With Phosphoryl Azide via Co(II)-Based Metalloradical Catalysisâ€�ÌýBeilstein J. Org. Chem.Ìý2014,Ìý10, 1282–1289. []

A chemistry diagram

90.ÌýÌýRuppel, J. V.; Cui, X.; Xu, X.; Zhang, X. P. “Stereoselective Intramolecular Cyclopropanation of alpha-Diazoacetates via Co(II)-Based Metalloradical Catalysisâ€�ÌýOrg. Chem. Front.Ìý2014,Ìý1, 515–520. []

A chemistry diagram

89.ÌýÌýJin, L.-M.; Lu, H.-J.; Cui, Y.; Lizardi, C. L.; Arzua, T. N.; Wojtas, L.; Cui, X.; Zhang, X. P. “Selective Radical Amination of Aldehydic C(sp2)‒H Bonds with Fluoroaryl Azides via Co(II)-Based Metalloradical Catalysis: Synthesis ofÌýN-Fluoroaryl Amides from Aldehydes under Neutral and Nonoxidative Conditionsâ€�ÌýChem. Sci.Ìý2014,Ìý5, 2422–2427. []

A chemistry diagram

88.ÌýÌýPaul, N. D.; Mandal, S.; Otte, M.; Cui, X.; Zhang, X. P.; de Bruin, B. “A Metalloradical Approach toÌý2H-Chromenesâ€�ÌýJ. Am. Chem. Soc.Ìý2014,Ìý136, 1090–1096. []

A chemistry diagram

87.ÌýÌýCui, X.; Zhang, X. P. “Asymmetric C–H Functionalization by Transition Metal-Catalyzed Carbene Transfer Reactionsâ€� InÌýComprehensive Organic Synthesis II (Second Edition)ÌýEds. Knochel, P.; Molander, G.; Amsterdam: Elsevier,Ìý2014, Vol. 7, pp. 86–120. []

86.ÌýÌýMaza, W. A.; Vetromile, G. M.; Kim, C.-S.; Xu, X.; Zhang, X. P.; Larsen, R. W. “Spectroscopic Investigation of the Noncovalent Association of the Nerve Agent Simulant Diisopropyl Methylphosphonate (DIMP) with Zinc(II)porphyrinsâ€�ÌýJ. Phys. Chem. A.Ìý2013,Ìý117, 11308–11315. []

A chemistry diagram

85.ÌýÌýXu, X.; Zhu, S.-F.; Cui, X.; Wojtas, L.; Zhang, X. P. “Cobalt(II)-Catalyzed Asymmetric Olefin Cyclopropanation with a-Ketodiazoacetatesâ€�ÌýAngew. Chem. Int. Ed.Ìý2013,Ìý52, 11857–11861. [] [Highlighted inÌý]

A chemistry diagram

84.ÌýÌýPaul, N. D.; Lu, H.-J.; Zhang, X. P.; de Bruin, B. “Carbene Radicals in Cobalt(II) Porphyrin-Catalyzed Carbene Carbonylation Reactions: A Catalytic Approach to Ketenesâ€�ÌýChem. Eur. J.Ìý2013,Ìý19, 12953–12958. []

A chemistry diagram

83.ÌýÌýLiu, L.; Xie, H.; Bostic, H. E.; Jin, L.-M.; Best, D. B.; Zhang, X. P.; Zhan, W. “Effects of Oriented Surface Dipole on Photoconversion Efficiency in an Alkane/Lipid-Hybrid-Bilayer-Based Photovoltaic Model Systemâ€�ÌýChemPhysChemÌý2013,Ìý14, 2777–2785. []

82.ÌýÌýCui, X.; Zhang, X. P. “Cobalt-Mediated Carbene Transfer Reactionsâ€� InÌýContemporary Carbene Chemistry; eds. Moss, R. A.; Doyle, M. P.; John Wiley & Sons,Ìý2013, Chapter 15, 491–525. []

81.ÌýÌýJin, L.-M.; Xu, X.; Lu, H.; Cui, X.; Wojtas, L.; Zhang, X. P. “Effective Synthesis of ChiralÌýN-Fluoroaryl Aziridines via Enantioselective Aziridination of Alkenes with Fluoroaryl Azidesâ€�ÌýAngew. Chem. Int. Ed.Ìý2013,Ìý52, 5309–5313. [] [Highlighted inÌý] [Highlighted inÌý]

A chemistry diagram

80.ÌýÌýCui, X.; Xu, X.; Wojtas, L.; Kim, M. M.; Zhang, X. P. “Regioselective Synthesis of Multisubstituted Furans via Metalloradical Cyclization of Alkynes with alpha-Diazocarbonyls: Construction of Functionalized alpha-Oligofuransâ€�ÌýJ. Am. Chem. Soc.Ìý2012,Ìý134, 19981–19984. [] [Highlighted inÌý] [Highlighted inÌý]

A chemistry diagram

79.ÌýÌýLu, H.-J.; Jiang, H.-L.; Hu, Y.; Wojtas, L.; Zhang, X. P. “Stereoselective Radical Amination of Electron-Deficient C(sp3)–H Bonds by Co(II)-Based Metalloradical Catalysis: Synthesis of alpha-Amino Acid Derivatives via alpha-C–H Amination of Esters and Amidesâ€�ÌýOrg. Lett.Ìý2012,Ìý14, 5158–5161. []

A chemistry diagram

78.ÌýÌýMeng, L.; Cheng, Q.; Kim, C.-S.; Gao, W.-Y.; Wojtas, L.; Chen, Y.-S.; Zaworotko, M. J.; Zhang, X. P.; Ma, S.-Q. “Crystal Engineering of a Microporous, Catalytically Active fcu Topology MOF Using a Custom-Designed Metalloporphyrin Linkerâ€�ÌýAngew. Chem. Int. Ed.Ìý2012,Ìý51, 10082–10085. [] [Selected asÌý]

A chemistry diagram

77.ÌýÌýJiang, H.-L.; Zhang, X. P. “Oxidation: C─N Bond Formation by Oxidation (Aziridines)â€� InÌýComprehensive Chirality; eds. Carreira, E. M.; Yamamoto, H.; Amsterdam: Elsevier,Ìý2012, Vol. 5, pp. 168–182. []Ìý

76.ÌýÌýWang, X.-S.; Chrzanowski, M.; Gao, W.-Y.; Kim, C.-S.; Wojtas, L.; Chen, Y.-S.; Zhang, X. P.; Ma, S.-Q. “Quest for HighlyÌýPorous Metal-Metalloporphyrin Framework Based upon A Custom-DesignedÌýOctatopic Porphyrin Ligandâ€�ÌýChem. Commun.Ìý2012,Ìý48, 7173–7175. []

A chemistry diagram

75.ÌýÌýHu, Y.; Zhang, X. P. “Selective Olefination of Carbonyl Compounds via Metal-Catalyzed Carbene Transfer from Diazo Reagentsâ€�ÌýTop. Curr. Res.Ìý2012,Ìý327, 147–162. []

74.ÌýÌýZhu, S.-F.; Cui, X.; Zhang, X. P. “Ligand Effect on Cobalt(II)-Catalyzed Asymmetric Cyclopropanation with Diazosulfones: Approaching High Stereoselectivity through Modular Design of D2-Symmetric Chiral Porphyrinsâ€�ÌýEur. J. Inorg. Chem.Ìý2012, 430–434. []

73.ÌýÌýBurda, W. N.; Fields, K. B.; Gill, J. B.; Burt, R.; Shepherd, M.; Zhang, X. P.; Shaw, L. N. “Neutral Metallated and Meso-Substituted Porphyrins as Antimicrobial Agents Against Gram-Positive Pathogensâ€�ÌýEur. J. Clin. Microbiol. Infect. Dis.Ìý2012,Ìý31, 327–335. []

72.ÌýÌýCui, X.; Zhang, X. P. “Iron(III) meso-Tetraphenylporphine Chlorideâ€�Ìýe-EROS, John Wiley & Sons,Ìý2012;ÌýDOI: 10.1002/047084289X.rn01388. []

71.ÌýÌýWang, X.-S.; Meng, L.; Cheng, Q.-G.; Kim, C.-S.; Wojtas, L.; Chrzanowski, M.; Chen, Y.-S.; Zhang, X. P.; Ma, S.-Q. “A Three-Dimensional Porous Metal-Metalloporphyrin Framework Consisting of Nanoscopic Polyhedral Cages with a High Density of Open Metal Sitesâ€�ÌýJ. Am. Chem. Soc.Ìý2011,Ìý133, 16322–16325. []

A chemistry diagram

70.ÌýÌýLu, H.-J.; Jiang, H.-L.; Hu, Y.; Wojtas, L.; Zhang, X. P. “Chemoselective Intramolecular Allylic C–H Amination over C=C Aziridination through Co(II)-Based Metalloradical Catalysisâ€�ÌýChem. Sci.Ìý2011,Ìý2, 2361–2366. [] [Highlighted inÌý]

A chemistry diagram

69.ÌýÌýXu, X.; Lu, H.-J.; Ruppel, J. V.; Cui, X.; de Mesa, S. L.; Wojtas, L.; Zhang, X. P. “Highly Asymmetric Intramolecular Cyclopropanation of Acceptor-Substituted Diazoacetates by Co(II)-Based Metalloradical Catalysis: Iterative Approach for Development of New Generation Catalystsâ€�ÌýJ. Am. Chem. Soc.Ìý2011,Ìý133, 15292–15295. [] [Highlighted inÌý]

A chemistry diagram

68.ÌýÌýLyaskovskyy, V.; Suarez, A. I. O.; Lu, H.-J.; Jiang, H.-L.; Zhang, X. P.; de Bruin, B. “Mechanism of Cobalt(II) Porphyrin-Catalyzed C–H Amination with Organic Azides: Radical Nature and H-Atom Abstraction Ability of Cobalt(III)-Nitrene Key Intermediatesâ€�ÌýJ. Am. Chem. Soc.Ìý2011,Ìý133, 12264–12273. []

A chemistry diagram

67.ÌýÌýLu, H.-J.; Dzik, W. I.; Xu, X.; Wojtas, L.; de Bruin, B.; Zhang, X. P. “Experimental Evidence for Cobalt(III)-Carbene Radicals: Key Intermediates in Cobalt(II)-Based Metalloradical Cyclopropanationâ€�ÌýJ. Am. Chem. Soc.Ìý2011,Ìý133, 8518–8521. []

A chemistry diagram

66.ÌýÌýBelof, J. L.; Cioce, C. R.; Xu, X.; Zhang, X. P.; Space, B.; Woodcock, H. L. “Characterization of Tunable Radical Metal-Carbenes: Key Intermediates in Catalytic Cyclopropanationâ€�,ÌýOrganometallicsÌý2011,Ìý30, 2739–2746. []

A chemistry diagram

65.ÌýÌýDzik, W. I.; Zhang, X. P.; de Bruin, B. “The Redox Non-Innocence of Carbene Ligands: Carbene Radicals in (Catalytic) C-C Bond Formationâ€�ÌýInorg. Chem.ÌýÌý2011,Ìý50, 9896–9903. []

A chemistry diagram

64.ÌýÌýUygun, A.; Myjavcova, R.; Yavuz, A. G.; Ruppel. J. V.; Fields, K. B.; Frankhauser, A.; Zhang, X. P.; Bhethanbotla, V. R.; Bednar, P. “Electrochemical Polymerization and Investigation of Properties of Poly(5-(4’-aminophenylamino)-10,20-diphenylporphyrin)â€�ÌýElectroanalysisÌý2011,Ìý23, 1158–1167. []

63.ÌýÌýSuarez, A. I. O.; Jiang, H.-L.; Zhang, X. P.; de Bruin, B. “The Radical Mechanism of Cobalt(II) Porphyrin-Catalyzed Olefin Aziridination and the Importance of Cooperative H-Bondingâ€�ÌýDalton Trans.ÌýÌý2011,Ìý40, 5697–5705. []

A chemistry diagram

62.ÌýÌýCui, X.; Xu, X.; Lu, H.-J.; Zhu, S.-F.; Wojtas, L.; Zhang, X. P. “Enantioselective Cyclopropenation of Alkynes with Acceptor/Acceptor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysisâ€�ÌýJ. Am. Chem. Soc.Ìý2011,Ìý133, 3304–3307. [] [Highlighted inÌý]

A chemistry diagram

61.ÌýÌýLu, H.-J.; Zhang, X. P. “Catalytic C–H Functionalization by Metalloporphyrins: Recent Development and Future Directionsâ€�ÌýChem. Soc. Rev.Ìý2011,Ìý40, 1899–1909. []

A chemistry diagram

60.ÌýÌýFields, K. B.; Engle, J. T.; Sripothongnak, S.; Kim, C.-S.; Zhang, X. P.; Ziegler, C. J. “Cobalt Carbaporphyrin-Catalyzed Cyclopropanationâ€�ÌýChem. Commun.Ìý2011,Ìý47, 749. []ÌýÌý

A chemistry diagram

59.ÌýÌýLu, H.-J.; Jiang, H.-L.; Wojtas, L.; Zhang, X. P. “Selective Intramolecular C–H Amination via Metalloradical Activation of Azides: Synthesis of 1,3-Diamines under Neutral and Nonoxidative Conditionsâ€�ÌýAngew. Chem. Int. Ed.Ìý2010,Ìý49, 10192–10196. [] [Selected asÌý][Highlighted inÌý]

A chemistry diagram

58.ÌýÌýZhan, W.; Jiang, K.; Smith, M. D.; Bostic, H. E.; Best, M. D.; Auad, M. L.; Ruppel, J. V.; Kim, C.-S.; Zhang, X. P. “Photocurrent Generation from Porphyrin/Fullerene Complexes Assembled in a Tethered Lipid Bilayerâ€�ÌýLangmuirÌý2010, 26, 15671–15679. []

A chemistry diagram

57.ÌýÌýHilker, B.; Fields, K. B.; Stern, A.; Space, B.; Zhang, X. P.; Harmon, J. P. “Dielectric Analysis of Poly(methyl methacrylate) Zinc(II) Mono-pinacolborane Diphenylporphyrin Compositesâ€�ÌýPolymerÌý2010, 51, 4790–4805. []

A chemistry diagram

56.ÌýÌýZhu, S.-F.; Xu, X.; Perman, J. A.; Zhang, X. P. “A General and Efficient Cobalt(II)-Based Catalytic System for Highly Stereoselective Cyclopropanation of Alkenes with a-Cyano-Diazoacetatesâ€�ÌýJ. Am. Chem. Soc.Ìý2010,Ìý132, 12796–12799. [] [Highlighted inÌý] [Highlighted inÌý]

A chemistry diagram

55.ÌýÌýDzik, W. I.; Xu, X.; Zhang, X. P.; Reek, J. N. H.; de Bruin, B. “Carbene Radicals’ in CoII(por)-Catalyzed Olefin Cyclopropanationâ€�ÌýJ. Am. Chem. Soc.Ìý2010,Ìý132, 10891–10902. []

A chemistry diagram

54.ÌýÌýLu, H.-J.; Tao, J.-R.; Jones, J. E.; Wojtas, L.; Zhang, X. P. “Co(II)-Catalyzed Intramolecular C–H Amination of Phosphoryl Azides: Formation of 6- and 7-Membered Cyclophosphoramidatesâ€�ÌýOrg. Lett.Ìý2010,Ìý12,Ìý1248–1251. [] [Highlighted inÌý]

A chemistry diagram

53.ÌýÌýLu, H.-J.; Subbarayan, V.; Tao, J.; Zhang, X. P. “Cobalt-Catalyzed Intermolecular Benzylic C–H Amination with 2,2,2-Trichloroethoxycarbonyl Azide (TrocN3)â€�ÌýOrganometallicsÌý2010,Ìý29, 389–393. []

A chemistry diagram

52.ÌýÌýRuppel, J. V.; Fields, K. B.; Snyder, N. L.; Zhang, X. P. “Metalloporphyrin-Catalyzed Asymmetric Atom/Group Transfer Reactionsâ€� InÌýHandbook of Porphyrin Science; eds. Kadish, K. M.; Smith, K. M.; Guilard, R.; World Scientific,Ìý2010, Vol. 10, Chapter 43, pp. 1–84. []

51.ÌýÌýFields, K. B.; Ruppel, J. V.; Snyder, N. L.; Zhang, X. P. “Porphyrin Functionalization via Carbon-Heteroatom Cross-Coupling Reactionsâ€� InÌýHandbook of Porphyrin Science; eds. Kadish, K. M.; Smith, K. M.; Guilard, R.; World Scientific,Ìý2010, Vol. 3, Chapter 13, pp. 367–428. []

50.ÌýÌýSubbarayan, V.; Ruppel, J. V.; Zhu, S.-F.; Perman, J. A.; Zhang, X. P. “Highly Asymmetric Cobalt-Catalyzed Aziridination of Alkenes with Trichloroethoxysulfonyl Azide (TcesN3)â€�ÌýChem. Commun.Ìý2009,Ìý4266–4268. []

A chemistry diagram

49.ÌýÌýRuppel, J. V.; Gauthier, T. J.; Snyder, N. L.; Perman, J. A.; Zhang, X. P. “Asymmetric Cobalt-Catalyzed Cyclopropanation with Succinimidyl Diazoacetate: General Synthesis of Optically Active Cyclopropyl Carboxamidesâ€�ÌýOrg. Lett.Ìý2009,Ìý11, 2273–2276. [] [Highlighted inÌý]Ìý

A chemistry diagram

48.ÌýÌýZhu, S.-F.; Zhang, X. P. “Cobalt(II) Acetateâ€�Ìýe-EROS, John Wiley & Sons,Ìý2009; DOI: 10.1002/047084289X.rc182.pub2. []

47.ÌýÌýZhu, S.-F.; Perman, J. A.; Zhang, X. P. “Acceptor/Acceptor-Substituted Diazo Reagents for Carbene Transfers: Cobalt-Catalyzed Asymmetric (Z)-Cyclopropanation of Alkenes with a-Nitro-Diazoacetatesâ€�ÌýAngew. Chem. Int. Ed.Ìý2008, 47, 8460–8463. [] [Highlighted inÌý] [Highlighted inÌý]

A chemistry diagram

46.ÌýÌýJones, J. E.; Ruppel, J. V.; Gao, G.-Y.; Thomas, M. M.; Zhang, X. P. “Cobalt-Catalyzed Asymmetric Olefin Aziridination with Diphenylphosphoryl Azideâ€�ÌýJ. Org. Chem.Ìý2008,Ìý73, 7260–7265. []

A chemistry diagram

45.ÌýÌýGao, G.-Y.; Ruppel, J. V.; Fields, K. B.; Xu, X.; Chen, Y.; Zhang, X. P. “Synthesis of Diporphyrins via Palladium-Catalyzed C–O Bond Formation: Effective Access to Chiral Diporphyrinsâ€�ÌýJ. Org. Chem.Ìý2008,Ìý73, 4855–4858. []

A chemistry diagram

44.ÌýÌýRuppel, J. V.; Jones, J. E.; Huff, C. A.; Kamble, R. M.; Chen, Y.; Zhang, X. P. “A Highly Effective Cobalt Catalyst for Olefin Aziridination with Azides: Hydrogen Bonding-Guided Catalyst Designâ€�ÌýOrg. Lett.Ìý2008,Ìý10, 1995–1998. []

A chemistry diagram

43.ÌýÌýZhu, S.; Ruppel, J. V.; Lu, H.; Wojtas, L.; Zhang, X. P. “Cobalt-Catalyzed Asymmetric Cyclopropanation with Diazosulfones: Rigidification and Polarization of Ligand Chiral Environment via Hydrogen Bonding and Cyclizationâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý2008,Ìý130, 5042–5043. [] [Highlighted inÌý] [Highlighted inÌý]

A chemistry diagram

42.ÌýÌýGao, G. Y.; Ruppel, J. V.; Allen, D. B.; Chen, Y.; Zhang, X. P. “Synthesis of beta-Functionalized Porphyrins via Palladium-Catalyzed Carbon–Heteroatom Bond Formations: Expedient Entry into beta-Chiral Porphyrinsâ€�ÌýJ. Org. Chem.Ìý2007,Ìý72, 9060–9066. []

A chemistry diagram

41.ÌýÌýHarden, J. D.; Ruppel, J. V.; Gao, G.-Y.; Zhang, X. P. “Cobalt-Catalyzed Intermolecular C–H Amination with Bromamine-T as Nitrene Sourceâ€�ÌýChem. Comm.Ìý2007,Ìý4644–4646. []

A chemistry diagram

40.ÌýÌýRuppel, J. V.; Kamble, R. M.; Zhang, X. P. “Cobalt-Catalyzed Intramolecular C–H Amination with Arylsulfonyl Azidesâ€�ÌýOrg. Lett.Ìý2007,Ìý9, 4889–4892. []

A chemistry diagram

39.ÌýÌýChen, Y.; Ruppel, J. V.; Zhang, X. P. “Cobalt-Catalyzed Asymmetric Cyclopropanation of Electron-Deficient Olefinsâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý2007,Ìý129, 12074–12075. [] [Highlighted inÌý] [Highlighted inÌý] [Highlighted inÌý]

A chemistry diagram

38.ÌýÌýChen, Y.; Zhang, X. P. “Asymmetric Cyclopropanation of Styrenes Catalyzed by Metal Complexes ofÌýD2-Symmetrical Chiral Porphyrin: Superiority of Cobalt over Ironâ€�ÌýJ. Org. Chem.Ìý2007,Ìý72, 5931–5934. [] [Highlighted inÌý]

A chemistry diagram

37.ÌýÌýGao, G.-Y.; Jones, J. E.; Vyas, R.; Harden, J. D.; Zhang, X. P. “Cobalt-Catalyzed Aziridination with Diphenylphosphoryl Azide (DPPA): Direct Synthesis ofÌýN-Phosphorous-Substituted Aziridines from Alkenesâ€�ÌýJ. Org. Chem.Ìý2006,Ìý71, 6655–6658. []

A chemistry diagram

36.ÌýÌýChen, Y.; Zhang, X. P. “Trans Effect on Cobalt Porphyrin Catalyzed Asymmetric Cyclopropanationâ€�ÌýSynthesisÌý2006,ÌýNo.10, 1697–1700. (Invited Contribution to Special Topic) []

A chemistry diagram

35.ÌýÌýGao, G.-Y.; Harden, J. D.; Zhang, X. P. “Cobalt-Catalyzed General and Efficient Aziridination of Alkenesâ€�ÌýOrg. Lett.Ìý2005,Ìý7, 3191–3193. []

A chemistry diagram

34.ÌýÌýChen, Y.; Gao, G.-Y.; Zhang, X. P. “Palladium-Mediated Synthesis of NovelÌýmeso-Chiral Porphyrins for Cobalt-Catalyzed Cyclopropanationâ€�ÌýTetrahedron Lett.Ìý2005,Ìý46, 4965–4969. []

A chemistry diagram

33.ÌýÌýBaskaran, D.; Mays, J. W.; Zhang, X. P.; Bratcher, M. S. “Carbon Nanotubes with Covalently Linked Porphyrin Antennae: Photoinduced Electron Transferâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý2005,Ìý127, 6916–6917. []

A chemistry diagram

32.ÌýÌýGao, G.-Y.; Colvin, A. J.; Chen, Y.; Zhang, X. P. “Synthesis ofÌýmeso-Arylsulfanyl- and Alkylsulfanyl-Substituted Porphyrins via Palladium-Mediated C–S Bond Formationâ€�ÌýJ. Org. Chem.Ìý2004,Ìý69, 8886–8892. []

A chemistry diagram

31.ÌýÌýChen, Y.; Fields, K. B.; Zhang, X. P. “Bromoporphyrins as Versatile Synthons for Modular Construction of Chiral Porphyrins: Cobalt-Catalyzed Highly Enantioselective and Diastereoselective Cyclopropanationâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý2004,Ìý126, 14718–14719.Ìý[] [Highlighted inÌý]

A chemistry diagram

30.ÌýÌýVyas, R.; Gao, G.-Y.; Harden, J. D.; Zhang, X. P. “Iron(III) Porphyrin-Catalyzed Aziridination of Alkenes with Bromamine-T as Nitrene Sourceâ€�ÌýOrg. Lett.Ìý2004,Ìý6, 1907–1910. []

A chemistry diagram

29.ÌýÌýGao, G.-Y.; Chen, Y.; Zhang, X. P. “General Synthesis ofÌýmeso-Amidoporphyrins via Palladium-Catalyzed Amidationâ€�ÌýOrg. Lett.Ìý2004,Ìý6, 1837–1840. []

A chemistry diagram

28.ÌýÌýChen, Y.; Zhang, X. P. “Vitamin B12ÌýDerivatives as Natural Asymmetric Catalysts: Enantioselective Cyclopropanation of Alkenesâ€�ÌýJ. Org. Chem.Ìý2004,Ìý69, 2431–2435.Ìý[]

A chemistry diagram

27.ÌýÌýLee, M.-Y.; Chen, Y.; Zhang, X. P. “General and Selective Olefination of Aldehydes and Ketones Catalyzed by a Cobalt(II) Porphyrin Complexâ€�ÌýOrganometallicsÌý2003,Ìý22, 4905–4909.Ìý[]

A chemistry diagram

26.ÌýÌýHuang, L.; Chen, Y.; Gao, G.-Y.; Zhang, X. P. “Diastereoselective and Enantioselective Cyclopropanation of Alkenes Catalyzed by Cobalt Porphyrinsâ€�ÌýJ. Org. Chem.Ìý2003,Ìý68, 8179–8184.Ìý[]

A chemistry diagram

25.ÌýÌýGao, G.-Y.; Colvin, A. J.; Chen, Y.; Zhang, X. P. “Versatile Synthesis ofÌýmeso-Aryloxy- and Alkoxy-Substituted Porphyrins via Palladium-Catalyzed C–O Cross-Coupling Reactionsâ€�ÌýOrg. Lett.Ìý2003,Ìý5, 3261–3264.Ìý[]

A chemistry diagram

24.ÌýÌýGao, G.-Y.; Chen, Y.; Zhang, X. P. “General and Efficient Synthesis of Arylamino- and Alkylamino-Substituted Diphenylporphyrins and Tetraphenylporphyrins via Palladium-Catalyzed Multiple Amination Reactionsâ€�ÌýJ. Org. Chem.Ìý2003,Ìý68, 6215–6221.Ìý[]

A chemistry diagram

23.ÌýÌýChen, Y.; Huang, L.; Zhang, X. P. “Acid-Promoted Olefination of Ketones by Iron(III) Porphyrin Complexâ€�ÌýOrg. Lett.Ìý2003,Ìý5, 2493–2496.Ìý[]

A chemistry diagram

22.ÌýÌýChen, Y.; Huang, L.; Zhang, X. P. “Efficient and Stereoselective Synthesis of beta-Trifluoromethyl-alpha, beta-Unsaturated Esters via Iron(III) Porphyrin-Catalyzed Olefination of Ketonesâ€�ÌýJ. Org. Chem.Ìý2003,Ìý68, 5925–5929.Ìý[]

A chemistry diagram

21.ÌýÌýChen, Y.; Zhang, X. P. “Facile and Efficient Synthesis ofÌýmeso-Arylamino- and Alkylamino-Substituted Porphyrins via Palladium-Catalyzed Aminationâ€�ÌýJ. Org. Chem.Ìý2003,Ìý68, 4432–4438.Ìý[]

A chemistry diagram

20.ÌýÌýChen, Y.; Huang, L.; Ranade, M. A.; Zhang, X. P. “Iron(III) and Ruthenium(II) Porphyrin Complexes-Catalyzed Selective Olefination of Aldehydes with Ethyl Diazoacetateâ€�ÌýJ. Org. Chem.Ìý2003,Ìý68, 3714–3717.Ìý[]

A chemistry diagram

19.ÌýÌýCui, W.; Zhang, X. P.; Wayland, B. B. “Bimetallo-Radical Carbon-Hydrogen Bond Activation of Methanol and Methaneâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý2003,Ìý125, 4994–4995.Ìý[]

18.ÌýÌýYin, J-J.; Rainka, M. P.; Zhang, X.-X.; Buchwald, S. L. “A Highly Active Suzuki Catalyst for the Synthesis of Sterically Hindered Biaryls: Novel Ligand Coordinationâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý2002,Ìý124,Ìý1162–1163. []

17.ÌýÌýZhang, X.-X.; Harris, M. C.; Sadighi, J. P.; Buchwald, S. L. “The Use of Palladium Chloride as A Precatalyst for the Amination of Aryl Bromidesâ€�ÌýCan.ÌýJ. Chem.Ìý2001,Ìý79, 1799–1805. []

16.ÌýÌýZhang, X.-X.; Buchwald, S. L. “Efficient Synthesis ofÌýN-Aryl-Aza-Crown Ethers via Palladium-Catalyzed Aminationâ€�ÌýJ. Org. Chem.Ìý2000,Ìý65, 8027–8031. []

15.ÌýÌýZhang, X.-X.; Lippard, S. J. “A Mixed-Valent Heptairon Chloride Cluster Supported by the Porphyrin-Linked Dicarboxylate Ligand PDKâ€�ÌýInorg. Chem.Ìý2000,Ìý39, 4388–4389. []

14.ÌýÌýZhang, X.-X.; Wayland, B. B. “Sterically Demanding Diporphyrin Ligands and Rhodium(II) Porphyrin Bimetalloradical Complexesâ€�ÌýInorg. Chem.Ìý2000,Ìý39, 5318–3525. []

13.ÌýÌýZhang, X.-X.; Sadighi, J. P.; Mackewitz, T. W.; Buchwald, S. L. “Efficient Synthesis of Well-Defined, High Molecular Weight, and Processible Polyanilines under Mild Conditions via Palladium-Catalyzed Aminationâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý2000,Ìý122, 7606–7607. []

12.ÌýÌýZhang, X.-X.; Lippard, S. J. “Synthesis of PDK, a Novel Porphyrin-Linked Dicarboxylate Ligandâ€�ÌýJ.ÌýOrg. Chem.Ìý2000,Ìý65, 5298–5305. []

11.ÌýÌýZhang, X.-X.; Fuhrmann, P.; Lippard, S. J. “Synthesis And Triiron Complexes of PDK, A New Porphyrin-Linked Dicarboxylate Ligandâ€�ÌýJ.ÌýAm. Chem. Soc.Ìý1998,Ìý120, 10260–10261. []

10.ÌýÌýZhang, X.-X.; Parks, F. P.; Wayland, B. B. “One-Electron Activation of CO by a Rhodium(II) Porphyrin Bimetalloradical Complex: Concerted Reactions of Two Metalloformyl Radicals ((MCO)·)â€�ÌýJ.ÌýAm. Chem. Soc.Ìý1997,Ìý119, 7938–7944. []

9.ÌýÌýDel Rossi, K. J.; Zhang, X.-X.; Wayland, B. B. “Reactions of C-H Bonds in Organic Oxygenates with Octaethylporphyrinato Rhodium(II) and Iridium(II) Dimersâ€�ÌýJ. Organomet. Chem.Ìý1995,Ìý504, 47–56. []

8.ÌýÌýZhang, X.-X.; Wayland, B. B. “Rhodium(II) Porphyrin Bimetalloradical Complexes: Preparation and Enhanced Reactivity with CH4Ìýand H2â€�ÌýJ. Am. Chem. Soc.Ìý1994,Ìý116, 7897–7898. []

7.ÌýÌýFrancesconi, L. C.; Yang, Y. Y.; Kung, M. P.; Zhang, X.-X.; Billings, J.; Guo, Y. Z.; Kung, H. F. “Technetium-99mÌý±·,±·â€™-Bis(2-mercapto-2-methylpropyl)-2-aminobenzylamine: Technetium-99m Complexes of a Novel Bis(aminoethanethiol) Ligandâ€�ÌýJ. Med. Chem.Ìý1994,Ìý37, 3282–3288. []

6.ÌýÌýLiu, B.-L.; Meng, Z.-X.; Zhang, X.-X.; Li, L. “Study on Structure-Activity Relationship of Cholesterol Analogs as Adrenal Imaging Agent with CNDO/2 Methodâ€�ÌýJ. IsotopesÌý1992,Ìý5, 1.

5.ÌýÌýZhang, X.-X.; Liu, B.-L. “The Structure-Activity Relationship of Cholesterol Analogs as Adrenal Imaging Agentsâ€�ÌýJ. IsotopesÌý1991,Ìý4, 234.

4.ÌýÌýZhang, X.-X.; Liu, B.-L. “New Cholesterol Analog as Adrenal Imaging Agent-Synthesis and Tissue Distribution of Bromine-82 Labeled 6-Bromomethylcholesterolâ€�ÌýJ. Nucl. Radiochem.Ìý1991,Ìý13, 49. []

3.ÌýÌýZhang, X.-X.; Liu, B.-L.; Jin, Y.-T.; Kung, H. F. “Development of Tc-99m-ECD as a New Brain Imaging Agent II. Kinetics of Ligand Exchange, Stability and Clinical Evaluationâ€�ÌýJ. IsotopesÌý1990,Ìý3, 137.

2.ÌýÌýZhang, X.-X.; Liu, B.-L.; Jin, Y.-T.; Kung, H. F. “Development of Tc-99m-ECD as a New Brain Imaging Agent I. Synthesis and Labelingâ€�ÌýJ. IsotopesÌý1990,Ìý3, 73.

1.ÌýÌýPan, Z.-Y.; Jin, Y.-T.; Liu, B.-L.; Zhang, X.-X. “Monkey and Human SPECT rCBF Imaging with Tc-99m-ECDâ€�ÌýJ. Nucl. Med.Ìý1989,Ìý9, 210.

Back To Top