| Year |
Citation |
Score |
| 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 |
0.64 |
|
| 2002 |
Zhao S, Smith KS, Deveau AM, Dieckhaus CM, Johnson MA, Macdonald TL, Cook JM. Biological activity of the tryprostatins and their diastereomers on human carcinoma cell lines. Journal of Medicinal Chemistry. 45: 1559-62. PMID 11931609 DOI: 10.1021/Jm0155953 |
0.414 |
|
| 2002 |
Zhao S, Liao X, Cook JM. Enantiospecific, stereospecific total synthesis of (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine as well as the total synthesis of the Alstonia bisindole macralstonidine. Organic Letters. 4: 687-90. PMID 11869102 DOI: 10.1021/Ol010222H |
0.593 |
|
| 1999 |
Ma C, He X, Liu X, Yu S, Zhao S, Cook JM. Effect of the leaving group on the alkylation diastereoselectivity of the Schollkopf chiral auxiliary Tetrahedron Letters. 40: 2917-2918. DOI: 10.1016/S0040-4039(99)00394-9 |
0.579 |
|
| 1999 |
Ma C, Liu X, Yu S, Zhao S, Cook JM. Concise synthesis of optically active ring-A substituted tryptophans Tetrahedron Letters. 40: 657-660. DOI: 10.1016/S0040-4039(98)02497-6 |
0.632 |
|
| 1998 |
Zhao S, Gan T, Yu P, Cook JM. Total synthesis of tryprostatin A and B as well as their enantiomers Tetrahedron Letters. 39: 7009-7012. DOI: 10.1016/S0040-4039(98)01466-X |
0.424 |
|
| 1997 |
Gan T, Liu R, Yu P, Zhao S, Cook JM. Enantiospecific Synthesis of Optically Active 6-Methoxytryptophan Derivatives and Total Synthesis of Tryprostatin A1 The Journal of Organic Chemistry. 62: 9298-9304. DOI: 10.1021/Jo971640W |
0.608 |
|
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