Phototransposition chemistry of methylisothiazoles and methylthiazoles

JW Pavlik, CR Pandit, CJ Samuel…

Index: Pavlik, James W.; Pandit, Chennagiri R.; Samuel, Christopher J.; Day, A. Colin Journal of Organic Chemistry, 1993 , vol. 58, # 12 p. 3407 - 3410

Full Text: HTML

Citation Number: 19

Abstract

Methylisothiazoles undergo phototransposition in neutral solution to methylthiazoles by a single permutation process. Methylisothiazole-methylisothiazole transpositions, previously reported to occur, were not detected in these reactions. In trifluoroacetic acid solvent, protonated methylisothiazoles and methylthiazoles phototranspose by P4 and P5 permutation pathways, respectively, resulting in a unique phototransposition cycle.