Tao Wang
Affiliations: | 2001 | University of Wisconsin-Milwaukee, Milwaukee, WI |
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Sign in to add mentorJames M. Cook | grad student | 2001 | UW-Milwaukee | |
(Enantiospecific total synthesis of (+)-vellosimine, (+)-normacusine B and (-)-norsuaveoline as well as an improved enantiospecific total synthesis of (+)-ajmaline and (+)-alkaloid G.) |
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Wang T, Shigdar S, Gantier MP, et al. (2015) Cancer stem cell targeted therapy: progress amid controversies. Oncotarget |
Yu J, Wang T, Liu X, et al. (2003) General approach for the synthesis of sarpagine indole alkaloids. Enantiospecific total synthesis of (+)-vellosimine, (+)-normacusine B, (-)-alkaloid Q3, (-)-panarine, (+)-Na-methylvellosimine, and (+)-Na-methyl-16-epipericyclivine. The Journal of Organic Chemistry. 68: 7565-81 |
Zhao S, Liao X, Wang T, et al. (2003) The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine, as well as the total synthesis of the alstonia bisindole alkaloid macralstonidine. The Journal of Organic Chemistry. 68: 6279-95 |
Yu J, Wang T, Wearing XZ, et al. (2003) Enantiospecific total synthesis of (-)-(E)16-epiaffinisine, (+)-(E)16-epinormacusine B, and (+)-dehydro-16-epiaffinisine as well as the stereocontrolled total synthesis of alkaloid G. The Journal of Organic Chemistry. 68: 5852-9 |
Wang T, Xu Q, Yu P, et al. (2001) Stereocontrolled total synthesis of alkaloid G via the oxy-anion Cope rearrangement and improved total synthesis of (+)-ajmaline. Organic Letters. 3: 345-8 |
Zheng T, Flippen-Anderson J, Yu P, et al. (2001) Stereocontrolled conversion of quinine into 10(R),11-dihydroxydihydroquinine via the sharpless osmylation process. The Journal of Organic Chemistry. 66: 1509-11 |
Yu P, Wang T, Li J, et al. (2000) Enantiospecific total synthesis of the sarpagine related indole alkaloids talpinine and talcarpine as well as the improved total synthesis of alstonerine and anhydromacrosalhine-methine via the asymmetric Pictet-Spengler reaction. The Journal of Organic Chemistry. 65: 3173-91 |
Liu X, Wang T, Xu Q, et al. (2000) Enantiospecific total synthesis of the enantiomer of the indole alkaloid affinisine Tetrahedron Letters. 41: 6299-6303 |
Li J, Wang T, Yu P, et al. (1999) General approach for the synthesis of ajmaline/sarpagine indole alkaloids: Enantiospecific total synthesis of (+)-ajmaline, alkaloid G, and norsuaveoline via the asymmetric Pictet-Spengler reaction Journal of the American Chemical Society. 121: 6998-7010 |
Wang T, Yu P, Li J, et al. (1998) The enantiospecific total synthesis of norsuaveoline Tetrahedron Letters. 39: 8009-8012 |