107344-62-7Relevant academic research and scientific papers
SYNTHESIS OF 4H-PYRROLO-BENZOTHIAZINES AND N-METHYL-1,3,4,5-TETRAHYDRO-2H-3-BENZAZEPIN-2-ONES
Wang, Huey-Min,Lin, Meng-Chiao,Chen, Ling-Ching
, p. 1519 - 1526 (2007/10/02)
Pummerer-type reaction was carried out with α-acyl sulfides and phenyliodine(III)bis(trifluoroacetate) instead of α-acyl sulfoxides to prepare 4H-pyrrolobenzothiazines and N-methyl-1,3,4,5-tetrahydro-2H-3-benzazepin-2-ones.
Synthesis of 4H-Pyrrolobenzothiazines and 3-(Methylthio)oxindoles
Wang, Huey-Min,Lin, Meng-Chiao,Chen, Ling-Ching
, p. 217 - 220 (2007/10/02)
The Pummerer reaction was carried out with α-acylsulfides and phenyl iodosyl bis(trifluoroacetate) instead of α-acylsulfoxides to prepare 4H-pyrrolobenzothiazines and 3-(methylthio)oxindoles.
Intramolecular Capture of Pummerer Rearrangement Intermediates. I. Synthesis of Pyrrolobenzothiazines
Bates, Dallas K.,Winters, R. Thomas,Burnell, A. Sell
, p. 695 - 699 (2007/10/02)
Treatment of 1-(2-alkylsulfinylphenyl)pyrroles with trifluoroacetic acid in refluxing toluene gives 4-substituted pyrrolobenzothiazines in good yield when the alkyl group bears an electron withdrawing substituent on the α-carbon.In the absence
