Synthesis and Reactions of 2-Benzoylmethyl-2-phenyl-4,6-di(phenylimino)-5H-1,3,5-dithiazinium Perchlorate.
✍ Scribed by T. E. Glotova; N. I. Protsuk; M. Yu. Dvorko; A. I. Albanov
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 16 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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## Abstract Starting from commercially available [2,3,4,5,6‐^2^H~5~]benzoic acid, [2,3,4,5,6‐^2^H~5~]phenyl glucosinolate was synthesized. Under negative‐ion electrospray‐ionization mass spectrometric conditions, this compound affords a peak at __m__/__z__ 399. Since this __m__/__z__ value is not k
## Abstract magnified image A new method for the synthesis of substituted 5‐(2‐hydroxyethyl)‐2‐phenylimino‐1,3‐thiazolidin‐4‐ones and 5‐(2‐hydroxyethyl)‐2‐phenylamino‐4,5‐dihydro‐1,3‐thiazol‐4‐ones is described, starting from phenylthioureas and 3‐bromotetrahydrofuran‐2‐one. The reaction proceeds