Electrophilic reactions of halides of group vi elements. 7. Reactions of allylbenzene and allyl phenyl ether with selenium tetrahalides View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1982-07

AUTHORS

Yu. V. Migalina, S. V. Galla-Bobik, S. M. Khripak, V. I. Staninets

ABSTRACT

The reaction of selenium tetrachloride with allylbenzene and allyl phenyl ether proceeds in accordance with the Markownikoff rule to give 1:2 adducts. The use of selenium tetrabromide changes the course of the reaction and leads to the production of a mixture of adducts in accordance with and counter to the Markownikoff rule, as well as products of cyclization of the intermediate monoadducts to 2-bromomethyl-2,3-dihydrobenzo[b]selenophene or 2-bromomethyl-benzo-1,4-selenoxane derivatives. More... »

PAGES

690-692

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00568943

DOI

http://dx.doi.org/10.1007/bf00568943

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1002817535


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