ChemInform Abstract: Selective Bromochlorination of endo-1,4-Dibromotricyclo(5.2.1.02,6) deca-3,8-diene-5,10-dione 10-Ethylene Acetal at the Conjugated Carbon- Carbon Double Bond

Autor:	J. Tsanaktsidis, K. J. Parker, R. W. Gable
Rok vydání:	2010
Předmět:	chemistry.chemical_classification Ethylene Diene Double bond Acetal General Medicine Conjugated system Medicinal chemistry Chloride chemistry.chemical_compound Thionyl chloride chemistry medicine Dimethylformamide Organic chemistry medicine.drug
Zdroj:	ChemInform. 25
ISSN:	0931-7597
DOI:	10.1002/chin.199436081
Popis:	Exposure of (1) to bromine in thionyl chloride/ dimethylformamide produced (5), the result of regio- and stereo-selective addition of bromine chloride across the carbonyl-conjugated double bond. The structure of (5) was determined by X-ray crystallography, and its mode of formation is discussed in terms of the carbonyl attack mechanism.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ada8af13181a314dec42ed62c713bba3 https://doi.org/10.1002/chin.199436081 Zobrazit plný text záznamu Plný text