An octahydro-3a,6-methanoazulen-5-one resulting from an intramolecular Friedel–Crafts acylation

Autor:	Carolyn Pratt Brock, A. Syed, David S. Watt, S. K. Richardson, M. R. Sabol
Rok vydání:	1994
Předmět:	Olefin fiber Ether General Medicine Crystal structure Medicinal chemistry Chloride General Biochemistry Genetics and Molecular Biology Acylation chemistry.chemical_compound chemistry Intramolecular force medicine Friedel–Crafts reaction Derivative (chemistry) medicine.drug
Zdroj:	Acta Crystallographica Section C Crystal Structure Communications. 50:106-108
ISSN:	0108-2701
DOI:	10.1107/s0108270193006675
Popis:	The compound (1S,3aR,4R,6S,8aS,9S)-1-tert-butoxy-9-chloro-2,3,3a,4,6,7,8,8a-octahydro-8a-methyl-4-methylthio-1H-3a,6-methanoazulen-5-one, C 17 H 27 ClO 2 S, was identified as the reaction product when the acid chloride formed from a trans-fused perhydroindane derivative underwent a Friedel-Crafts acylation of the internal olefin
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7248be0ce67e5dc6d155c993128e6fc5 https://doi.org/10.1107/s0108270193006675 Zobrazit plný text záznamu Plný text