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Facile rearrangement of push-pull 5-substituted 4-oxothiazolidines induced by pyridinium hydrobromide perbromide under homogeneous reaction conditions

Efikasno premeštanje push-pull 5-supstituisanih 4-oksotiazolidina indukovano piridinijum-hidrobromid-perbromidom pod homogenim reakcionim uslovima

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2004
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Authors
Marković, Rade
Baranac, Marija M.
Džambaski, Zdravko
Article (Published version)
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Abstract
Pyridinium hydrobromide perbromide (PHBP) is a highly efficient reagent for the conversion of 5-substituted-2-alkylidene-4-oxothiazolidine derivatives to the corresponding thiazolidines with two fully delocalized exocyclic double bonds at the C(2) and C(5) positions. This conversion as a two-step bromination-rearrangement process occurs in acetonitrile under homogeneous reaction conditions.
Piridinijum-hidrobromid-perbromid (PHBP) je veoma efikasan reagens za konverziju 5-supstituisanih-2-alkiliden-4-oksotiazolidinskih derivata u odgovarajuće tiazolidine sa dve potpuno delokalizovane egzociklične dvogube veze u položajima C(2) i C(5). Ova konverzija je dvofazni proces bromovanja i premeštanja koji se odvija u acetonitrilu pod homogenim reakcionim uslovima.
Keywords:
thiazolidine / rearrangement / pyridinium hydrobromide perbromide / acetonitrile
Source:
Journal of the Serbian Chemical Society, 2004, 69, 4, 239-245
Publisher:
  • Serbian Chemical Society

DOI: 10.2298/JSC0404239M

ISSN: 0352-5139

WoS: 000220932200001

Scopus: 2-s2.0-2442638838
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URI
http://cer.ihtm.bg.ac.rs/handle/123456789/150
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