1. Deshydrohalogenations en acetyleniques par extraction de paires d'ions
2. The structure of this compound was confirmed by the agreement of its IR and NMR spectra with those of an authentic sample prepared by the method described in ref. 4. [3a: Oil, lit.4177°/2 mm. IR (neat): 3500 (OH), 1310 (SO2), 1405 (SO2), 730 and 685 cm-1(Ph). NMR (CDCl3): δ 3.17 (s, 1H), 3.20 (t, 2H), 3.71 (t, 2H), 7.3–8.1 (m, 5H)]
3. Yamamoto, T., Kobayashi, K. and Kimura, I. The 45th Annual Meeting of Chem. Soc. Japan, Preprint II. pp.847
4. 375. The fission of the thioether linkage in certain β-sulphonyl-sulphides
5. S, S-DIARYL- AND S-(2-SUBSTITUTED ETHYL)-S-PHENYL-N-TOSYLSULFILIMINES FROM CHLORAMINE T UNDER PTC CONDITIONS