Autor:	Th. Posternak, F. G. Cocu, G. Wolczunowicz, L. Bors
Rok vydání:	1970
Předmět:	Inorganic Chemistry Hydroxylation chemistry.chemical_compound Stereochemistry Chemistry Organic Chemistry Drug Discovery Stereoselectivity Physical and Theoretical Chemistry Biochemistry Catalysis
Zdroj:	Helvetica Chimica Acta. 53:2288-2295
ISSN:	0018-019X
DOI:	10.1002/hlca.19700530843
Popis:	Two new cyclopentane-pentols, namely the 1, 2, 3, 4/5- and 1, 2, 3/4, 5-isomers have been prepared by hydroxylation of the three 3, 4, 5-trihydroxy-1-cyclopentenes. The stereoselectivity of some hydroxylating agents is discussed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::bedd1e700db02aee271285b6c89ba8b1 https://doi.org/10.1002/hlca.19700530843 Zobrazit plný text záznamu Plný text