Stereoselective Total Synthesis of Iso-Cladospolide B and the 12 Membered-Macrolactone (6S,12R)-6-Hydroxy-12-methyloxacyclododecane-2,5-dione

Autor:	Palakodety Radha Krishna, Venkata Satyanarayana Mallula, Pendyala Venkata Arun Kumar
Rok vydání:	2015
Předmět:	Stereochemistry Organic Chemistry Diol Total synthesis Biochemistry Catalysis Inorganic Chemistry chemistry.chemical_compound chemistry Drug Discovery Organic chemistry Stereoselectivity Iso-cladospolide B Physical and Theoretical Chemistry Sharpless asymmetric dihydroxylation
Zdroj:	Helvetica Chimica Acta. 98:1115-1126
ISSN:	0018-019X
DOI:	10.1002/hlca.201500030
Popis:	Total syntheses of iso-cladospolide B (1) and the 12-membered macrolactone (6S,12R)-6-hydroxy-12-methyloxacyclododecane-2,5-dione (2), a non-natural product, were achieved from a common intermediate starting from commercially available 1,9-nonane diol.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::0ae0134b2c7df4f361b986aa6b54d6f1 https://doi.org/10.1002/hlca.201500030 Zobrazit plný text záznamu Plný text ve formátu PDF