Zobrazeno 1 - 10
of 48
pro vyhledávání: '"F. J. Swinbourne"'
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 97:157-163
The effects of ring modification on the mass spectral fragmentations of 2, 3-diaryl-1, 3-thiazolidin-4-ones were established by comparing their spectra with those of their S-oxides and with compounds in which the aromatic groups at C(2) or N(3) had b
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 78:223-235
The infra-red spectra of a series of 2,3-diaryl-1,3-thiazolidin-4-ones were measured and the majority of the absorption bands assigned. The value of the carbonyl stretching frequency was related to the availability of the lone pair on the nitrogen at
Publikováno v:
Organic Mass Spectrometry. 28:445-450
The mass spectral fragmentations of some 2,3-diaryl-1,3-thiazolidin-4-ones were established by comparing spectra and by using exact mass measurements. The major fragment ions were identified and their relative importances related to substituent effec
Publikováno v:
ChemInform. 22
Autor:
R. J. CREMLYN, F. J. SWINBOURNE, P. BASSIN, D. DANE, K. HIGGINS, P. MITCHELL, J. A. S. CAVALEIRO, F. J. DOMINGUES, M. DIAS
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 24
Publikováno v:
Magnetic Resonance in Chemistry. 30:1075-1078
The 13C NMR spectra of a series of 2,3-diaryl-1,3-thiazolidin-4-ones were measured and the resonance signals produced by the methylene, methine and carbonyl groups of the heterocyclic ring assigned. The variations in their chemical shifts were examin
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 57:173-179
The chlorosulfonation of a number of unsymmetrical benzils gave substituted benzofurans. Ring closure is dependent upon the electronic character of the substituent groups and can be controlled by electron-withdrawing groups. The reaction of the 2-thi
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 56:245-275
The early work on sulfonation, chlorosulfonation and the formation of sulfonyl derivatives was reviewed by Suter1 and by Suter and Weston for aromatic hydrocarbons.2 More recent reviews of sulfonation were carried out by Gilbert3 4 Hogg5 Cerfontain6