He Xu, Ph.D.
Affiliations: | 2007 | Temple University, Philadelphia, PA, United States |
Area:
Asymmetric SynthesisGoogle:
"He Xu"Parents
Sign in to add mentorFranklin Arnold Davis | grad student | 2007 | Temple University | |
(Asymmetric synthesis of nitrogen -containing heterocycles via enantiopure sulfinimines.) |
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Publications
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Adamczyk L, Adkins JK, Agakishiev G, et al. (2015) Azimuthal Anisotropy in U+U and Au+Au Collisions at RHIC. Physical Review Letters. 115: 222301 |
Ding Y, Xiang X, Gu M, et al. (2015) Efficient lipase-catalyzed Knoevenagel condensation: utilization of biocatalytic promiscuity for synthesis of benzylidene-indolin-2-ones. Bioprocess and Biosystems Engineering |
Davis FA, Xu H. (2012) Formal synthesis of (-)-Clavepictine A and (+)- Clavepictine B from A sulfinimine (N-sulfinylimine)- Derived chiral building block Heterocycles. 84: 1227-1233 |
Davis FA, Bowen KA, Xu H, et al. (2008) Synthesis of polysubstituted pyrroles from sulfinimines (N-sulfinyl imines). Tetrahedron. 64: 4174-4182 |
Davis FA, Xu H, Zhang J. (2007) Asymmetric synthesis of ring functionalized trans-2,6-disubstituted piperidines from N-sulfinyl delta-amino beta-keto phosphonates. total synthesis of (-)-myrtine. The Journal of Organic Chemistry. 72: 2046-52 |
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 |
Davis FA, Zhang J, Li Y, et al. (2005) Asymmetric synthesis of 2,4,5-trisubstituted piperidines from sulfinimine-derived δ-amino β-ketoesters. Formal synthesis of pseudodistomin B triacetate Journal of Organic Chemistry. 70: 5413-5419 |
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, Lee SH, Xu H. (2004) Asymmetric synthesis of cyclic α-amino phosphonates using masked oxo sulfinimines (n-sulfinyl imines) Journal of Organic Chemistry. 69: 3774-3781 |