Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Michael J. Suggate"'
Autor:
Gregory S. Coumbarides, Raymond Vincent Heavon Jones, Michael J. Suggate, Marco Dingjan, Ewan Boyd, Svitlana Buksha, Jason Eames, Rachel A. Stenson, Majid Motevalli
Publikováno v:
Journal of Chemical Crystallography. 37:233-241
The conformational arrangements of a series of enol acetates derived from simple ketones have been examined by X-ray crystallography. For this series, the carbonyl enol motif was found to adopt a similar conformation.
Autor:
Jason Eames, Ewan Boyd, Gregory S. Coumbarides, Michael J. Suggate, Ray V.H. Jones, Majid Motevalli, Rachel A. Stenson
Publikováno v:
Journal of Chemical Crystallography. 36:263-269
The conformational arrangement of a series of (R,R)-N,N′-tetrasubstituted cyclohexyl-1,2-diamines have been examined by X-ray crystallography.
Autor:
Jason Eames, Gregory S. Coumbarides, Svitlana Buksha, Neluka Weerasooriya, Michael J. Suggate, Marco Dingjan
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:757-771
Results are reported on the regioselective C-deuteriation of a series of silyl enol ethers derived from aryl alkyl ketones using deuterium (D2) gas as the deuterium source and palladium-on-barium sulfate as the mediator. These results highlight the n
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:153-161
The specific rotation of a variety of differential isotopomers is reported. The difference in their specific rotation appears to be greater than their percentage mass difference and each isotopomer seems to rotate (the plane of) plane-polarized light
Autor:
Gregory S. Coumbarides, Michael J. Suggate, Jason Eames, Mothia Begum, Marco Dingan, Sameer Chavda, Neluka Weerasooriya
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:707-732
Results are reported on the regioselective C-deuteriation of 2-methyl-tetralone using a series of D-sources and tertiary amines as potential mediators. The results presented further aid the understanding of kinetic deuteriation of both ‘base-contai
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 49:641-652
Results are reported on the regioselective C-deuteriation of a series of enolates derived from the deprotonation of aryl alkyl ketones using dilithiated urea as the pro-base in the presence of a suitable deuterium donor. Copyright © 2006 John Wiley
Autor:
Majid Motevalli, Jason Eames, Ewan Boyd, Raymond Vincent Heavon Jones, Rachel A. Stenson, Gregory S. Coumbarides, Michael J. Suggate
Publikováno v:
Tetrahedron Letters. 46:3473-3478
The synthesis of N , N ′-unsymmetrically tetrasubstituted cyclic 1,2-diamines derived from (1 R ,2 R )-diaminocyclohexane is reported. We comment on the structural nature of these cyclic 1,2-diamines and discuss their characteristic features.
Autor:
Gregory S. Coumbarides, Raymond Vincent Heavon Jones, Ewan Boyd, Jason Eames, Michael J. Suggate, Rachel A. Stenson
Publikováno v:
Tetrahedron Letters. 46:3479-3484
The synthesis of N , N ′-trisubstituted 1,2-diamines can be achieved by simple reduction of an aminal derived from (1 R ,2 R )-diaminocyclohexane. We comment on the scope and limitation of this reduction and discuss its application towards the synt
Autor:
Michael J. Suggate, Jason Eames, Gregory S. Coumbarides, Svitlana Buksha, Marco Dingjan, Neluka Weerasooriya
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 48:337-352
Results are reported on the regioselective C-deuteriation of a series of enol acetates (derived from the aryl alkyl ketones) using molecular deuterium as the D-source and palladium-on-barium sulphate as the mediator. The results presented highlight p
Autor:
Jason Eames, Michael J. Suggate
Publikováno v:
Angewandte Chemie. 117:190-193