A stereocontrolled total synthesis of optically active (R,R)-phytol

Autor:	Tamotsu Fujisawa, Toshio Sato, Kazuo Ohashi, Tatsuo Kawara
Rok vydání:	1981
Předmět:	Phytol chemistry.chemical_compound Stereospecificity Chemistry Stereochemistry Organic Chemistry Drug Discovery Total synthesis Optically active Biochemistry
Zdroj:	Tetrahedron Letters. 22:4823-4826
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(01)92354-8
Popis:	A stereospecific synthesis of (R,R)-phytol uith highly stereochemioal purity in both absolute and geometrical aonfigurations uas achieved by utilizing the SNZ type ring-opening reaction of (R)-β-methyl-β-propiolactone, and the SNZ′ type ring-opening reaction of isopropenyl oxirane, from (R)-pulegone as a starting material.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::9ffd5b6a884913c78458fb5039a4b73b https://doi.org/10.1016/s0040-4039(01)92354-8 Zobrazit plný text záznamu