Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Peter B. Coulter"'
Autor:
Peter B. Coulter, V. E. Wilson, W. B. Jennings, Derek R. Boyd, M. R. Mcguckin, Narain D. Sharma
Publikováno v:
ChemInform. 21
Autor:
W. Brian Jennings, Valerie E. Wilson, Derek R. Boyd, M. Rosaleen McGuckin, Narain D. Sharma, Peter B. Coulter
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :301
The oxidation of N-alkyl imines by m-chloroperoxybenzoic acid to yield nitrones was facilitated by (i) the presence of C-aryl substituents, (ii) steric inhibition of attack at the imino C-atom, (iii) electron donating para-substituents on the C-aryl
Publikováno v:
Organic Magnetic Resonance. 21:279-286
13C chemical shifts for several series of cis- and trans-N-alkylimines and oxaziridines bearing para-substituted C-phenyl rings are reported and correlated with dual substituent parameters. The 13CN and oxaziridine ring carbon shifts correlate primar
Publikováno v:
Tetrahedron Letters. 26:1673-1676
Steric and mesomeric effects have a marked influence upon the formation of oxaziridine (normal pathway) or nitrone (abnormal pathway) products from the imine-peroxyacid reaction; n.m.r. studies of the thermal isomerization of oxaziridines to nitrones
Publikováno v:
Chemischer Informationsdienst. 15
The formation of oxaziridines and the isomeric amides in equal amounts by the spontaneous autoxidation of several liquid imines via peroxyimidic acid intermediates is reported.
Publikováno v:
Tetrahedron Letters. 25:2287-2288
The results of a kinetic study of the thermal isomerization of oxaziridines derived from para -substituted C-arylaldimines and C-diarylketimines to the isomeric nitrones is reported.
Autor:
Rose M. Campbell, Derek R. Boyd, W. Brian Jennings, David C. Neill, James Grimshaw, Peter B. Coulter
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :849
Optically active oxaziridines have been synthesized with a maximum optical yield of 31% by photoisomerization (λ > 300 nm) of achiral aldo- and keto-nitrones in the presence of the chiral solvent (+)-(S) or (–)-(R)-2,2,2-trifluoro-1-phenylethanol.
Autor:
Michael E. Stubbs, Norris Thompson, Derek R. Boyd, Peter B. Coulter, Narain D. Sharma, Robert Hamilton
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2123
A range of oxaziridines containing N-methylene substituents has been synthesized by peracid oxidation of the corresponding fluorenylidene N-alkylamines. Spontaneous and tertiary amine base-catalysed decomposition of the oxaziridines into unstable NH