Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Michael G. Orchard"'
Autor:
Anthony P. Davis, Michael G. Orchard, Hongyu Li, Laurent Chabanne, Johnathan V. Matlock, Robert A. Tromans, Thomas Carter, Matthew P. Crump
Publikováno v:
Tromans, R A, Carter, T S, Chabanne, L, Crump, M P, Li, H, Matlock, J V, Orchard, M G & Davis, A P 2019, ' A biomimetic receptor for glucose ', Nature Chemistry, vol. 11, no. 1, pp. 52-56 . https://doi.org/10.1038/s41557-018-0155-z
Specific molecular recognition is routine for biology, but has proved difficult to achieve in synthetic systems. Carbohydrate substrates are especially challenging, because of their diversity and similarity to water, the biological solvent. Here we r
Autor:
Anthony P. Davis, Michael G. Orchard
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :919-924
A second ‘cholaphane’ framework is manifested in the title compound 8, which has been prepared from methyl 3α,7α, 12α-triacetoxycholanoate 9 in 23% overall yield. The synthesis involves the Knoevenagel condensation of ketone 11 with malononitr
Autor:
Michael G. Orchard, Anthony P. Davis
Publikováno v:
ChemInform. 24
A second ‘cholaphane’ framework is manifested in the title compound 8, which has been prepared from methyl 3α,7α, 12α-triacetoxycholanoate 9 in 23% overall yield. The synthesis involves the Knoevenagel condensation of ketone 11 with malononitr
Publikováno v:
ChemInform. 22
The ‘cholaphane’1 was synthesized in 26% overall yield from cholic acid and its structure determined by X-ray crystallography; the molecule adopts an open conformation and is able to surround two molecules of tetrahydrofuran.
Publikováno v:
ChemInform. 24
Knoevenagel condensations between t-butylcyclohexanone and malononitrile, Meldrum's acid and ethyl cyanoacetate gave electron-deficient alkenes which underwent equatorial-selective attack by chemoselective aryl organometallic reagents. Further transf
Publikováno v:
Tetrahedron. 48:8725-8738
Knoevenagel condensations between t-butylcyclohexanone and malononitrile, Meldrum's acid and ethyl cyanoacetate gave electron-deficient alkenes which underwent equatorial-selective attack by chemoselective aryl organometallic reagents. Further transf
Autor:
Michael G. Orchard, et al. et al.
Publikováno v:
ChemInform. 35
Publikováno v:
J. Chem. Soc., Chem. Commun.. :612-614
The ‘cholaphane’1 was synthesized in 26% overall yield from cholic acid and its structure determined by X-ray crystallography; the molecule adopts an open conformation and is able to surround two molecules of tetrahydrofuran.
Autor:
Anthony P. Davis, Michael G. Orchard
Publikováno v:
Tetrahedron Letters. 33:5111-5112
Methyl cholanoates with protected amino groups in either or both of the 7β- and 12β-positions have been synthesized from cholic acid 1 via sulphonylation, azide displacement and reduction.