Regioselectivity of the allylation of benzothiophene

Autor:	Yu. N. Radyukin, A. Karakhanov, Alexander V. Anisimov, Yu. N. Luzikov, V. M. Nikolaeva, E. A. Viktorova
Rok vydání:	1977
Předmět:	chemistry.chemical_compound chemistry Organic Chemistry Thiophene Organic chemistry Regioselectivity Benzothiophene Carbon-13 NMR Allyl halides Mass spectrometry
Zdroj:	Chemistry of Heterocyclic Compounds. 13:1296-1298
ISSN:	1573-8353 0009-3122
Popis:	The reaction of benzothiophene with allyl halides in the presence of silver trichloroacetate in chlorine-containing hydrocarbons was investigated. It was established by gas-liquid chromatography and 13C NMR and mass spectrometry that 3-allylbenzothiophene and diallylbenzothiophene are formed in this case. The 13C NMR spectra were interpreted on the basis of an additive scheme with the utilization of benzothiophene, thiophene, and 2- and 3-allylthiophenes as models.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::bf5f287d96f0c49f8e8238f992ed3e3b https://doi.org/10.1007/bf00469887 Zobrazit plný text záznamu Full text from SpringerLink