Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Richard T. Buck"'
Publikováno v:
ARKIVOC, Vol 2002, Iss 8, Pp 16-33 (2002)
Externí odkaz:
https://doaj.org/article/52dde512973b4f33b6e88580068af2fe
Autor:
Diane M. Coe, Leigh Ferris, Martin James Drysdale, Christopher J. Moody, J. Bobby Sanghera, Richard T. Buck, David Haigh, Neil D. Pearson
Publikováno v:
Tetrahedron: Asymmetry. 14:791-816
Decomposition of methyl 2-diazophenylacetate in the presence of silanes and a chiral dirhodium(II) catalyst results in SiH insertion of the intermediate carbenoid with varying degrees of enantioselectivity. New chiral dirhodium(II) carboxylate cat
Autor:
Diane Mary Coe, Paul A. Clarke, Richard T. Buck, Neil D. Pearson, Leigh Ferris, Martin James Drysdale, David Haigh, Elizabeth Swann, Christopher J. Moody
Publikováno v:
Chemistry - A European Journal. 6:2160-2167
A different approach to the synthesis of dipeptides is described based on the formation of the NHCHR1CONH-CHR2CO bond by carbenoid N-H insertion, rather than the formation of the peptide bond itself. Thus decomposition of triethyl diazophosphonoaceta
Autor:
Martin James Drysdale, Neil D. Pearson, Richard T. Buck, Christopher J. Moody, Diane Mary Coe
Publikováno v:
Tetrahedron Letters. 39:7181-7184
New chiral dirhodium(II) carboxylate catalysts for asymmetric carbenoid SiH insertion reactions have been identified using solution phase parallel synthesis techniques.
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :591-600
A new method for the synthesis of oxazoles, and in particular chiral non-racemic oxazoles derived from amino acids, has been developed. Thus, rhodium(II) catalysed reaction of diazocarbonyl compounds 6 and 11 in the presence of amides 8 and 10 result
Autor:
Leigh Ferris, Neil D. Pearson, David C. Forbes, Martin James Drysdale, Christopher J. Moody, David Haigh, Qi-Lin Zhou, Michael P. Doyle, Richard T. Buck
Publikováno v:
Tetrahedron Letters. 37:7631-7634
Decomposition of methyl 2-diazophenylacetate in the presence of dimethylphenylsilane and a chiral dirhodium(II) catalyst results in SiH insertion of the intermediate carbenoid with varying degrees of enantioselectivity (up to 47% ee).
Autor:
Enrique Aller, Martin James Drysdale, Christopher J. Moody, David Haigh, J. Bobby Sanghera, Neil D. Pearson, Leigh Ferris, Richard T. Buck
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2879-2884
Rhodium(II) acetate-catalysed decomposition of diazophenylacetates 1 and 3 in the presence of a range of N–H compounds results in an N–H insertion reaction of the intermediate carbenoids and formation of N-substituted phenylglycine derivatives 2
Autor:
N. D. Pearson, Leigh Ferris, M. J. Drysdale, Richard T. Buck, J. B. Sanghera, David Haigh, Enrique Aller, Christopher J. Moody
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 28
Autor:
Leigh Ferris, Michael P. Doyle, Neil D. Pearson, David C. Forbes, Qi-Lin Zhou, Richard T. Buck, Christopher J. Moody, David Haigh, Martin James Drysdale
Publikováno v:
ChemInform. 28
Decomposition of methyl 2-diazophenylacetate in the presence of dimethylphenylsilane and a chiral dirhodium(II) catalyst results in SiH insertion of the intermediate carbenoid with varying degrees of enantioselectivity (up to 47% ee).