Stereoselective synthesis of simplactone B via Prins cyclisation

Autor:	M. Somi Reddy, K. Rama Rao, Mendu Narender
Rok vydání:	2007
Předmět:	Stereochemistry Chemistry Yield (chemistry) Organic Chemistry Drug Discovery Stereoselectivity Biochemistry Combinatorial chemistry Simplactone
Zdroj:	Tetrahedron. 63:11011-11015
ISSN:	0040-4020
DOI:	10.1016/j.tet.2007.08.049
Popis:	The synthesis of simplactone B has been achieved through a series of nine steps in 85% overall yield using Prins cyclisation as the key step with high stereochemical control.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::4392f76eebb8725386818762e8f9adcb https://doi.org/10.1016/j.tet.2007.08.049 Zobrazit plný text záznamu Full Text from ScienceDirect