Поисковый запрос: (<.>S=ДИГИДРОКСИЛИРОВАНИЕ<.>) |
Общее количество найденных документов : 10
Показаны документы с 1 по 10
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1.
| 6'7'-dihydroxybergamottin contributes to the grapefruit juice effect // Clin. Pharmacol. and Ther., 2004. Vol. 75, N 6.-С.569-579
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2.
| 6'7'-dihydroxybergamottin contributes to the grapefruit juice effect // Clin. Pharmacol. and Ther., 2004. Vol. 75, N 6.-С.569-579
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3.
| Haddock John D. Dihydroxylation and dechlorination of chlorinated biphenyls by purified biphenyl 2,3-dioxygenase from Pseudomonas sp. strain LB400 // J. Bacteriol., 1995. Vol. 177, N 1.-С.20-26
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4.
| Haddock John D. Dihydroxylation and dechlorination of chlorinated biphenyls by purified biphenyl 2,3-dioxygenase from Pseudomonas sp. strain LB400 // J. Bacteriol., 1995. Vol. 177, N 1.-С.20-26
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5.
| Haddock John D. Dihydroxylation and dechlorination of chlorinated biphenyls by purified biphenyl 2,3-dioxygenase from Pseudomonas sp. strain LB400 // J. Bacteriol., 1995. Vol. 177, N 1.-С.20-26
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6.
| The cytochrome P450 2B6 (CYP2B6) is the main catalyst of efavirenz primary and secondary metabolism: Implication for HIV/AIDS therapy and utility of efavirenz as a substrate marker of CYP2B6 catalytic activity // J. Pharmacol. and Exp. Ther., 2003. Vol. 306, N 1.-С.287-300
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7.
| The cytochrome P450 2B6 (CYP2B6) is the main catalyst of efavirenz primary and secondary metabolism: Implication for HIV/AIDS therapy and utility of efavirenz as a substrate marker of CYP2B6 catalytic activity // J. Pharmacol. and Exp. Ther., 2003. Vol. 306, N 1.-С.287-300
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8.
| Toshima Total synthesis of (+)-(2S,3R)-piscidic acid via catalytic asymmetric dihydroxylation of a trisubstituted olefin // Biosci., Biotechnol. and Biochem., 1999. Vol. 63, N 5.-С.964-967
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9.
| Дигидроксилирование дегидроэпиандростерона в положениях 7'альфа' и 15'альфа' мицелиальными грибами // Прикл. биохимия и микробиол., 2009. Т. 45, N 6.-С.684-689
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10.
| Дигидроксилирование дегидроэпиандростерона в положениях 7'альфа' и 15'альфа' мицелиальными грибами // Прикл. биохимия и микробиол., 2009. Т. 45, N 6.-С.684-689
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