Intramolecular sulfenylation using sulfoxides. Preparation of N-alkyl pyrrolo[2,1-b]- [1,3,4]benzothiadiazines
Document Type
Article
Publication Date
1-1-1996
Abstract
Refluxing sulfoxides 5a,b, prepared in four steps from 2-(ethylthio)aniline, in p-xylene solution promotes electrophilic ring closure to produce 6a,b by loss of ethanol.
Publication Title
Heterocyclic Communications
Recommended Citation
Bates, D.,
Tafel, K.,
&
Xu, J.
(1996).
Intramolecular sulfenylation using sulfoxides. Preparation of N-alkyl pyrrolo[2,1-b]- [1,3,4]benzothiadiazines.
Heterocyclic Communications,
2(2), 115-116.
http://doi.org/10.1515/HC.1996.2.2.115
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p/13460
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