Studies on the regio- and enantioselectivity of the lipase-catalyzed transesterification of 1′- and 2′-naphthyl alcohols in organic solvent

Autor:	Patrizia Ferraboschi, Enzo Santaniello, Ada Manzocchi, Silvana Casati
Rok vydání:	1995
Předmět:	biology Chemistry Organic solvent Organic Chemistry Pseudomonas Transesterification biology.organism_classification Catalysis Inorganic Chemistry biology.protein Organic chemistry Physical and Theoretical Chemistry Lipase
Zdroj:	Tetrahedron: Asymmetry. 6:1521-1524
ISSN:	0957-4166
Popis:	The Pseudomonas cepacia lipase preferentially acylates the 2′-regioisomers of a few 1′- and 2′-naphthyl alcohols; in the case of compounds 3a, 3c, 4a, 4c the (R)-alcohols (65→98% ee) and the (S)-acetates (62–98% ee) are formed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::60f3fcef482acb38853f1023fe72ab93 https://doi.org/10.1016/0957-4166(95)00188-u Zobrazit plný text záznamu Full Text from ScienceDirect