Exploiting novel 2-(tert-butyldimethylsiloxy)thiophene (1, TBSOT) as versatile carbon nucleophile and both enantiomers of glyceraldehyde acetonide as chiral sources, an entry to both enantiomers of anti HIV-active 2',3'-dideoxy-4'-thiocytidine 10 and ent-lO was devised and executed
2-(tert-Butyldimethylsiloxy)thiophene: Application to Total Syntheses of Both Enantiomers of 2',3'-Dideoxy-4'-thiocytidine
Pietro Spanu;
1995
Abstract
Exploiting novel 2-(tert-butyldimethylsiloxy)thiophene (1, TBSOT) as versatile carbon nucleophile and both enantiomers of glyceraldehyde acetonide as chiral sources, an entry to both enantiomers of anti HIV-active 2',3'-dideoxy-4'-thiocytidine 10 and ent-lO was devised and executedFile in questo prodotto:
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