Conformation of cyclohexane ring in some polycyclic molecules

Autor:	N. A. Alekperov, Anatoly N. Vereshchagin, R. S. Salakhova, M. S. Salakhov, S. G. Vul'fson, A. P. Timosheva, N. É. Musaeva
Rok vydání:	1975
Předmět:	chemistry.chemical_compound Cyclohexane Diene Bicyclic molecule Stereochemistry Chemistry Maleic anhydride Molecule General Chemistry Hexachlorocyclopentadiene Ring (chemistry) Medicinal chemistry Methyl group
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 24:785-790
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf00920694
Popis:	1. When the cyclohexane ring is trans-condensed with a five-membered anhydride ring and a bicyclic system the C-C bonds of the bicyclic system occupy equatorial positions. 2. The stereochemistry of the diene synthesis of hexachlorocyclopentadiene with the anhydrides of cis- and trans-3-methyl-4-cyclohexene-1,2-dicarboxylic acids is determined by the configuration of the methyl group. 3. The addition of maleic anhydride to the diene system of the anhydride of 1,2,3,4-tetracehlorobicyclo[4.4.0]decadiene-8,9-dicarboxylic acid goes in the trans-position to the bonds of the cyclohexane ring.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d2d91b7a98e5b270c788d114bf238fdb https://doi.org/10.1007/bf00920694 Zobrazit plný text záznamu Full text from SpringerLink