Autor:	M.T. Saindane, K.G. Marathe
Rok vydání:	1975
Předmět:	chemistry.chemical_compound Stereospecificity Stereochemistry Chemistry Dihydropyran Mesylate Organic Chemistry Drug Discovery Ether Solvolysis Biochemistry
Zdroj:	Tetrahedron. 31:2821-2824
ISSN:	0040-4020
DOI:	10.1016/0040-4020(75)80297-3
Popis:	Stereochemistry of cyanomaclurin is confirmed by a stereospecific synthesis of (±) epicyanomaclurin trimethyl ether and the solvolysis of its mesylate to the former. The earlier prediction that the dihydropyran protons should have small coupling in both the isomers in this cage structure is also confirmed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::82718cc410529d885b52af3429535347 https://doi.org/10.1016/0040-4020(75)80297-3 Zobrazit plný text záznamu