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Tao Wang - Publications

Affiliations: 
2001 University of Wisconsin-Milwaukee, Milwaukee, WI 
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11 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Wang T, Shigdar S, Gantier MP, Hou Y, Wang L, Li Y, Al Shamaileh H, Yin W, Zhou SF, Zhao X, Duan W. Cancer stem cell targeted therapy: progress amid controversies. Oncotarget. PMID 26496035 DOI: 10.18632/oncotarget.6176  0.354
2003 Yu J, Wang T, Liu X, Deschamps J, Flippen-Anderson J, Liao X, Cook JM. 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. PMID 14510528 DOI: 10.1021/Jo030006H  0.704
2003 Zhao S, Liao X, Wang T, Flippen-Anderson J, Cook JM. 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. PMID 12895062 DOI: 10.1021/Jo030055U  0.678
2003 Yu J, Wang T, Wearing XZ, Ma J, Cook JM. 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. PMID 12868917 DOI: 10.1021/Jo030116O  0.533
2001 Wang T, Xu Q, Yu P, Liu X, Cook JM. Stereocontrolled total synthesis of alkaloid G via the oxy-anion Cope rearrangement and improved total synthesis of (+)-ajmaline. Organic Letters. 3: 345-8. PMID 11428010 DOI: 10.1021/Ol000331G  0.679
2001 Zheng T, Flippen-Anderson J, Yu P, Wang T, Mirghani R, Cook JM. Stereocontrolled conversion of quinine into 10(R),11-dihydroxydihydroquinine via the sharpless osmylation process. The Journal of Organic Chemistry. 66: 1509-11. PMID 11312991 DOI: 10.1021/Jo0015321  0.37
2000 Yu P, Wang T, Li J, Cook JM. 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. PMID 10814213 DOI: 10.1021/Jo000126E  0.538
2000 Liu X, Wang T, Xu Q, Ma C, Cook JM. Enantiospecific total synthesis of the enantiomer of the indole alkaloid affinisine Tetrahedron Letters. 41: 6299-6303. DOI: 10.1016/S0040-4039(00)01061-3  0.721
1999 Li J, Wang T, Yu P, Peterson A, Weber R, Soerens D, Grubisha D, Bennett D, Cook JM. 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. DOI: 10.1021/Ja990184L  0.713
1998 Wang T, Yu P, Li J, Cook JM. The enantiospecific total synthesis of norsuaveoline Tetrahedron Letters. 39: 8009-8012. DOI: 10.1016/S0040-4039(98)01788-2  0.517
1997 Peng Y, Wang T, Fuxiang Y, Cook JM. General Approach for the synthesis of macroline/sarpagine related indole alkaloids Via the asymmetric pictet-spengler reaction: the enantiospecific synthesis of the Na-H, azabicyclo[3.3.1]nonone template Tetrahedron Letters. 38: 6819-6822. DOI: 10.1016/S0040-4039(97)01603-1  0.511
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