Investigation of the halocyclization of S- and N-allyl derivatives of 2-benzothiazolethione

dc.contributor.author	Kim D.G.	en
dc.contributor.author	Sudolova N.M.	en
dc.contributor.author	Slepuhin P.A.	en
dc.date.accessioned	2018-10-15T11:18:25Z
dc.date.available	2018-10-15T11:18:25Z
dc.date.issued	2011
dc.identifier.issn	93122
dc.identifier.uri	http://dspace.susu.ru/handle/0001.74/20120
dc.description.abstract	3-Allyl-2-benzothiazolethione reacts with iodine regiospecifically with annelation of the five-membered ring, while with bromine a mixture of the five- and six-membered rings are formed. 2-Allylthioben- zothiazole reacts with halogens with annelation of the five- and six-membered rings, while 2-(2-methyl-2-propenyl)thiobenzothiazole is annelated at the five-membered ring. © 2011 Springer Science+Business Media, Inc.	en]
dc.language.iso	English
dc.relation.ispartof	Chemistry of Heterocyclic Compounds	en]
dc.title	Investigation of the halocyclization of S- and N-allyl derivatives of 2-benzothiazolethione	en
dc.type	Article	en]
dc.identifier.doi	10.1007/s10593-011-0808-y
dc.identifier.scopus	https://www.scopus.com/inward/record.uri?eid=2-s2.0-80755135487&doi=10.1007%2fs10593-011-0808-y&partnerID=40&md5=2aac25b19f38acc27a9bfb588284971f

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