38090-55-0Relevant articles and documents
INTRAMOLECULAR CYCLIZATION OF O-ALKYL-N-(3-PHENYLPROPENOYL)THIOCARBAMATES CATALYZED BY BORON TRIFLUORIDE
Dzurilla, Milan,Kutschy, Peter,Koscik, Dusan,Toma, Stefan
, p. 710 - 717 (2007/10/02)
2-Alkoxy-6-phenyl-5,6-dihydro-4H-1,3-thiazin-4-ones, 6-phenyl-1,3-perhydrothiazine-2,4-dione and S-methyl N-(3-phenylpropenoyl)thiocarbamate are the products of intramolecular rearrangement of O-alkyl N-(3-phenylpropenoyl)thiocarbamates catalyzed by boron
CYCLISATIONS OF 1,3-THIAZINE-2,4-DIONES AND RELATED SYSTEMS
Vliet, P. N. W. Van Der,Hamersma, J. A. M.,Speckamp, W. N.
, p. 2007 - 2014 (2007/10/02)
Thiazinediones 10 and 11 serve as starting materals for intramolecular amidoalkylations.While the stability of the derived hydroxy lactams 14 and 15 is lower as compared to carbocyclic analogs the ring closures to the bicyclic systems indicate a common order of reactivity of the corresponding N-acyliminium intermediate, e.g. 26.