Enantiospecific synthesis of 8-epipuupehedione from ( R )-(−)-carvone

Autor:	Basudeb Achari, Chandana Giri, Sujaya Sengupta, Asish Kr. Banerjee, Soumen Maiti
Rok vydání:	2001
Předmět:	chemistry.chemical_compound Carvone chemistry Stereochemistry Metabolite Organic Chemistry Drug Discovery 8-epipuupehedione Organic chemistry Biochemistry Methylenedioxy
Zdroj:	Tetrahedron Letters. 42:2389-2391
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(01)00153-8
Popis:	An enantiospecific synthesis of the antitumor marine sponge metabolite puupehedione (2a) and its C8-epimer 2b as their methylenedioxy derivatives 8a and 8b was achieved through concomitant O-allyl deprotection and electrocyclization of 20 derived from (−)-carvone.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a40b78229c8d174d2afa91009c4e45ec https://doi.org/10.1016/s0040-4039(01)00153-8 Zobrazit plný text záznamu Full Text from ScienceDirect