Chiral enol acetates derived from prochiral oxabicyclic ketones using enzymes
摘要:
Racemic enol acetates 2-4 and 9 derived from prochiral 8-oxabicyclo[3.2.1]oct-6-en-3-ones have been resolved with good enantioselectivity (E=45, 47, 48 and 7.8, respectively) using silica-adsorbed Humicola sp. lipase and the absolute configuration of enol acetate 2 was determined by X-ray crystallographic analysis of the camphanyl derivative 13. (C) 1999 Elsevier Science Ltd. All rights reserved.
Chiral enol acetates derived from prochiral oxabicyclic ketones using enzymes
摘要:
Racemic enol acetates 2-4 and 9 derived from prochiral 8-oxabicyclo[3.2.1]oct-6-en-3-ones have been resolved with good enantioselectivity (E=45, 47, 48 and 7.8, respectively) using silica-adsorbed Humicola sp. lipase and the absolute configuration of enol acetate 2 was determined by X-ray crystallographic analysis of the camphanyl derivative 13. (C) 1999 Elsevier Science Ltd. All rights reserved.