Zobrazeno 1 - 10
of 12
pro vyhledávání: '"David J. Hotchkiss"'
Autor:
Sarah F. Jenkinson, David J. Hotchkiss, Andrew R. Cowley, George W. J. Fleet, David J. Watkin
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 1, Pp o294-o295 (2008)
The Kiliani reaction on 1-deoxy-(N,N-dimethylamino)-d-fructose, itself readily available from reaction of dimethylamine and d-glucose, proceeded to give access to the title β-sugar amino acid, C15H27NO7. X-ray crystallography determined the stereoch
Externí odkaz:
https://doaj.org/article/4a37953c02264a9d9e995e5a458c8a8b
Autor:
Joseph M. D. Cook, Christopher C. Harding, George W. J. Fleet, David J. Watkin, David J. Hotchkiss
The title compound, C 20H 25NO 4, the product formed in the Amadori rearrangement of L-rhamnose with dibenzylamine, is shown by X-ray crystallographic analysis to be a rare example of an Amadori product crystallizing in a furanose form. © 2005 Inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c5c18d51a718d32712ab266fc1d0504
https://ora.ox.ac.uk/objects/uuid:efea6f2c-7c4e-4437-9386-41c06cb84981
https://ora.ox.ac.uk/objects/uuid:efea6f2c-7c4e-4437-9386-41c06cb84981
Autor:
David J. Watkin, Loren L. Parry, Vanessa Eastwick-Field, David J. Hotchkiss, George W. J. Fleet
The ring size of both the lactone and the ketal protecting group in the title compound, C9H14O5, have been established by X-ray crystallographic analysis. The crystal structure consists of hydrogen-bonded spirals parallel to the b axis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d8627d706f1980b00e883ad41c7c836
https://ora.ox.ac.uk/objects/uuid:bfda109f-3190-4074-b057-2462cd2c0612
https://ora.ox.ac.uk/objects/uuid:bfda109f-3190-4074-b057-2462cd2c0612
Autor:
Sarah F. Jenkinson, David J. Hotchkiss, George W. J. Fleet, Kathrine V. Booth, David J. Watkin
The unknown relative configurations in the title compound, C13H13N3O4, of the acetal carbon and of the quaternary carbon bearing the azide were determined by X-ray crystallographic analysis; the absolute configuration was defined by the use of 2-C-me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e26ffc723d5c0bcdd7a27849db04ab46
https://ora.ox.ac.uk/objects/uuid:ece2135f-43ec-467f-b71b-f5661b9c7c41
https://ora.ox.ac.uk/objects/uuid:ece2135f-43ec-467f-b71b-f5661b9c7c41
Autor:
Vanessa Eastwick-Field, Alexander C. Weymouth-Wilson, Kathrine V. Booth, George W. J. Fleet, Raquel G. Soengas, David J. Hotchkiss
Saccharinic acids, branched 2-C-methyl-aldonic acids, may be accessed via a green procedure from aldoses by sequential conversion to an Amadori ketose and treatment with calcium hydroxide; d-galactose and d-glucose are converted to 2-C-methyl-d-lyxon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11bb8a3b08992f11774629e8bb746c78
https://doi.org/10.1016/j.tetlet.2006.11.137
https://doi.org/10.1016/j.tetlet.2006.11.137
Publikováno v:
Tetrahedron Letters. 47:315-318
Saccharinic acids (2- C -methyl aldonic acids) may be formed by treatment of Amadori ketoses with calcium hydroxide or by the Kiliani reaction of 1-deoxy ketoses with cyanide. Thus (i) N , N -dibenzyl or N , N -dimethyl-1-amino-1-deoxy- d -fructose w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8d936b9c0e049baf205cb92b6a09299
https://doi.org/10.1016/j.tetlet.2005.11.018
https://doi.org/10.1016/j.tetlet.2005.11.018
Autor:
Alexander C. Weymouth-Wilson, Thomas Heinz, Sarah F. Jenkinson, Robert Clarkson, George W. J. Fleet, Filipa P. da Cruz, David J. Hotchkiss, Nigel A. Jones, Kathrine V. Booth
Publikováno v:
TETRAHEDRON-ASYMMETRY. 19(20)
Readily crystallized 2-C-methyl-d-ribono-1,4-lactone is formed in a one-pot procedure from d-glucose without any protecting groups by treatment with dimethylamine to give an Amadori ketose and then with aqueous calcium hydroxide in yields of approxim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0458628803b46925a24d205e23d33868
http://ora.ox.ac.uk/objects/uuid:9a3c3d1c-d54e-4e2e-aea5-5cbe5f7eff45
http://ora.ox.ac.uk/objects/uuid:9a3c3d1c-d54e-4e2e-aea5-5cbe5f7eff45
Publikováno v:
TETRAHEDRON-ASYMMETRY. 18(4)
The value of readily available 2-C-methyl aldonic acids in short syntheses of carbon branched piperidines containing quaternary centers is demonstrated. The effect of the introduction of a 4-C-methyl group into piperidine imino sugar inhibitors of l-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::030ccd2d52a3a41908db3789689ee6c0
http://ora.ox.ac.uk/objects/uuid:b2cae2ab-0735-4d03-8aff-411d561bc401
http://ora.ox.ac.uk/objects/uuid:b2cae2ab-0735-4d03-8aff-411d561bc401
Autor:
David J. Hotchkiss, Christopher C. Harding, David J. Watkin, Andrew R. Cowley, George W. J. Fleet, Francesco Punzo
The title tagatosamine, C20H25NO5.CH 4O, formed in the Amadori rearrangement of D-galactose with dibenzylamine, is shown to crystallize as the α-anomer, in contrast to the β-anomer formed in the Amadori reaction of D-glucose with dibenzylamine. ©
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa334cfb34e13c64f50243af8ad6d423
http://hdl.handle.net/20.500.11769/56008
http://hdl.handle.net/20.500.11769/56008
The title rhamnopyranosylamine, C 13H 19NO 4·1.5H 2O, was isolated as an intermediate in the Amadori rearrangement of L-rhamnose with p-toluidine. Two independent molecules and three water molecules of crystallization comprise the asymmetric unit, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::731a160049b07d4b546d6ffdbc786a2d
http://hdl.handle.net/20.500.11769/14590
http://hdl.handle.net/20.500.11769/14590