Total synthesis of (−)-cleistenolide

Autor:	Palakuri Ramesh, Harshadas M. Meshram
Rok vydání:	2011
Předmět:	Natural product biology Organic Chemistry Total synthesis biology.organism_classification Biochemistry Cleistenolide Acetonide chemistry.chemical_compound chemistry Annonaceae Drug Discovery Salt metathesis reaction Organic chemistry Cleistochlamys kirkii
Zdroj:	Tetrahedron Letters. 52:2443-2445
ISSN:	0040-4039
Popis:	The total synthesis of (−)-cleistenolide, a novel natural product recently isolated from the annonaceae species cleistochlamys kirkii oliver, is described. The synthesis proceeds starting from easily accessible d -manitol using a selective benzoylation, a selective acetonide deprotection, silylprotection and ring-closing metathesis reaction.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::80274e296046574f1dbda8dd32cb73fc https://doi.org/10.1016/j.tetlet.2011.01.124 Zobrazit plný text záznamu Full Text from ScienceDirect