Year |
Citation |
Score |
2022 |
Zhang Z, Fu B, Wang X, Hu Z, Liu X, Wang T, Zhao J. Synthesis of ()-β-Chloro-enamides via a Base-Promoted -Hydroamidation of Alkynyl Chlorides Using 1,1-Dichloroalkenes as Precursor. The Journal of Organic Chemistry. PMID 35686467 DOI: 10.1021/acs.joc.2c00581 |
0.342 |
|
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 |
0.342 |
|
2015 |
Yang Q, He Y, Wang T, Zeng L, Zhang Z. Synthesis of 3-heteroarylchromones via a photochemical reaction. Molecular Diversity. PMID 26197992 DOI: 10.1007/s11030-015-9620-4 |
0.312 |
|
2012 |
Liang Y, Jiang X, Fu XF, Ye S, Wang T, Yuan J, Wang Y, Yu ZX. Total synthesis of (+)-asteriscanolide: further exploration of the rhodium(I)-catalyzed [(5+2)+1] reaction of ene-vinylcyclopropanes and CO. Chemistry, An Asian Journal. 7: 593-604. PMID 22223465 DOI: 10.1002/Asia.201100805 |
0.32 |
|
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 |
0.72 |
|
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 |
0.716 |
|
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 |
0.593 |
|
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 |
0.712 |
|
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 |
0.384 |
|
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 |
0.621 |
|
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 |
0.695 |
|
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 |
0.699 |
|
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 |
0.595 |
|
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 |
0.583 |
|
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