Spirastrellolide B: The Synthesis of Southern (C9−C25) Region

Autor:	Annareddy Syamprasad Reddy, Srivari Chandrasekhar, Chegondi Rambabu
Rok vydání:	2008
Předmět:	Biological Products chemistry.chemical_compound Natural product chemistry Dihydroxylation Stereochemistry Organic Chemistry Organic chemistry Spiro Compounds Spirastrellolide B Macrolides Physical and Theoretical Chemistry Biochemistry
Zdroj:	Organic Letters. 10:4355-4357
ISSN:	1523-7052 1523-7060
DOI:	10.1021/ol801771s
Popis:	A combination of "chiron" and "asymmetric" approaches is utilized to construct the southern (C 9-C 25) region of marine natural product spirastrellolide B. The key functionalities are derived from d-glucose and Sharpless asymmetric epoxidation and dihydroxylation.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b493e0ee59bc1982abe24d4fd6b7923c https://doi.org/10.1021/ol801771s Zobrazit plný text záznamu