Yongzhong Wu, Ph.D.

Affiliations: 
2005 Temple University, Philadelphia, PA, United States 
Area:
Asymmetric Synthesis
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"Yongzhong Wu"
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Franklin Arnold Davis grad student 2005 Temple University
 (Asymmetric synthesis of nitrogen-containing bioactive compounds via enantiopure sulfinimines.)
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Lei H, Lei L, Shi J, et al. (2020) No expenditure difference among patients with liver cancer at stage IIV: Findings from a multicenter cross-sectional study in China. Chinese Journal of Cancer Research = Chung-Kuo Yen Cheng Yen Chiu. 32: 516-529
Davis FA, Zhang J, Wu Y. (2011) Total syntheses of (+)-monomorine I and (-)-indolizidine 195B from sulfinimine-derived 3-oxo pyrrolidine 2-phosphonates Tetrahedron Letters. 52: 2054-2057
Davis FA, Zhang J, Qiu H, et al. (2008) Asymmetric synthesis of cis- and trans-2,5-disubstituted pyrrolidines from 3-oxo pyrrolidine 2-phosphonates: synthesis of (+)-preussin and analogs. Organic Letters. 10: 1433-6
Li P, Evans CD, Wu Y, et al. (2008) Evolution of the total syntheses of ustiloxin natural products and their analogues. Journal of the American Chemical Society. 130: 2351-64
Davis FA, Xu H, Wu Y, et al. (2006) Asymmetric synthesis of polyfunctionalized pyrrolidines from sulfinimine-derived pyrrolidine 2-phosphonates. Synthesis of pyrrolidine 225C. Organic Letters. 8: 2273-6
Ramachandar T, Wu Y, Zhang J, et al. (2006) (S)‐(+)‐2,4,6‐Trimethylbenzenesulfinamide Organic Syntheses. 131-140
Davis FA, Nolt MB, Wu Y, et al. (2005) Asymmetric synthesis of β-amino carbonyl compounds with N-sulfinyl β-amino Weinreb amides Journal of Organic Chemistry. 70: 2184-2190
Davis FA, Yang B, Deng J, et al. (2005) Asymmetric synthesis using sulfinimines (N-sulfinyl imines) Phosphorus, Sulfur and Silicon and the Related Elements. 180: 1109-1117
Davis FA, Wu Y, Xu H, et al. (2004) Asymmetric synthesis of cis-5-substituted pyrrolidine 2-phosphonates using metal carbenoid NH insertion and δ-amino β-ketophosphonates Organic Letters. 6: 4523-4525
Davis FA, Wu Y. (2004) Asymmetric synthesis of the carbocyclic nucleoside building block (R)-(+)-4-aminocyclopentenone using δ-amino β-ketophosphonates and ring-closing metathesis (RCM) Organic Letters. 6: 1269-1272
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