Hongjun Zhang, Ph.D.

Affiliations: 
2006 Emory University, Atlanta, GA 
Area:
synthesis of heterocyclic compounds
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"Hongjun Zhang"
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Albert Padwa grad student 2006 Emory
 (Application of the intramolecular Diels -Alder reaction (IMDAF) of 2-amidofurans toward alkaloid synthesis.)
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Publications

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Li D, Zhang H, Lyons TW, et al. (2021) Comprehensive Strategies to Bicyclic Prolines: Applications in the Synthesis of Potent Arginase Inhibitors. Acs Medicinal Chemistry Letters. 12: 1678-1688
Pu Q, Zhang H, Guo L, et al. (2020) Discovery of Potent and Orally Available Bicyclo[1.1.1]pentane-Derived Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitors. Acs Medicinal Chemistry Letters. 11: 1548-1554
Nicolaou KC, Wang Y, Lu M, et al. (2016) Streamlined Total Synthesis of Uncialamycin and Its Application to the Synthesis of Designed Analogues for Biological Investigations. Journal of the American Chemical Society
Nicolaou KC, Ortiz A, Zhang H, et al. (2010) Total synthesis and structural revision of vannusals A and B: synthesis of the originally assigned structure of vannusal B. Journal of the American Chemical Society. 132: 7138-52
Nicolaou KC, Ortiz A, Zhang H, et al. (2010) Total synthesis and structural revision of vannusals A and B: synthesis of the true structures of vannusals A and B. Journal of the American Chemical Society. 132: 7153-76
Nicolaou KC, Ortiz A, Zhang H. (2010) Synthesis of Vannusal B Synfacts. 2010: 18-18
Nicolaou KC, Ortiz A, Zhang H. (2009) The true structures of the vannusals, part 2: Total synthesis and revised structure of vannusal B. Angewandte Chemie (International Ed. in English). 48: 5648-52
Nicolaou KC, Zhang H, Ortiz A. (2009) The true structures of the vannusals, part 1: Initial forays into suspected structures and intelligence gathering. Angewandte Chemie (International Ed. in English). 48: 5642-7
Nicolaou KC, Zhang H, Ortiz A, et al. (2008) Total synthesis of the originally assigned structure of vannusal B. Angewandte Chemie (International Ed. in English). 47: 8605-10
Boonsombat J, Zhang H, Chughtai MJ, et al. (2008) A general synthetic entry to the pentacyclic strychnos alkaloid family, using a [4 + 2]-cycloaddition/rearrangement cascade sequence. The Journal of Organic Chemistry. 73: 3539-50
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