Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Josie C. Briggs"'
Publikováno v:
Tetrahedron. 53:3943-3956
Ketosteroids absorbed into various insoluble supports (powdered polyethylene, microporous 2% crosslinked polystyrene beads, macroporous highly crosslinked polystyrene beads, silica gel and alumina) can be reduced using aqueous potassium borohydride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c0121f1291beb9fb938690db41b43c5
https://doi.org/10.1016/s0040-4020(97)00011-2
https://doi.org/10.1016/s0040-4020(97)00011-2
Autor:
Josie C. Briggs, Alan H. Haines
Publikováno v:
Carbohydrate Research. 282:293-298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07bfbf571b92438ba62225c76b893658
https://doi.org/10.1016/0008-6215(95)00379-7
https://doi.org/10.1016/0008-6215(95)00379-7
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :27-32
A range of (halogenomethyl)phenyl α-D-glucopyranosides 2–7, prepared from corresponding methylphenyl glucosides by synthetic manipulation of the aglycone moiety, have been investigated as enzyme-activated irreversible inhibitors of yeast α-glucos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9606e4501db43f8d1d82034be0b89a5
https://doi.org/10.1039/p19950000027
https://doi.org/10.1039/p19950000027
Publikováno v:
Reactive Polymers. 19:73-80
Prochiral ketones absorbed into chiral polymer supports were reduced with aqueous potassium borohydride. 2-Substituted naphthoquinones absorbed into chiral polymer supports were epoxidized using aqueous alkaline hydrogen peroxide. In both systems asy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8efea7d0112b30bb62a9efa1fb2140cc
https://doi.org/10.1016/0923-1137(93)90012-5
https://doi.org/10.1016/0923-1137(93)90012-5
Publikováno v:
ChemInform. 23
2-Chloromethyl-4-nitrophenyl α-D-glucopyranoside, prepared by a novel, four-step route from 2-methylphenyl α-D-glucopyranoside tetraacetate, is highly effective as an enzyme-activated irreversible inhibitor of yeast α-glucosidase and is much super
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2f4c170d6920ead0205623748bf85d1
https://doi.org/10.1002/chin.199245260
https://doi.org/10.1002/chin.199245260
Autor:
Josie C. Briggs, Alan H. Haines
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c2b75f1c5cc05b39eac1291afe52cb9
https://doi.org/10.1002/chin.199631186
https://doi.org/10.1002/chin.199631186
Autor:
Alan Lloyd, Ian Gibson, Richard J. K. Taylor, Alan P. Dawson, Silkie Meiners, Jackie Hook, Josie C. Briggs, Alan H. Haines
Publikováno v:
Carbohydrate Research. 234:23-35
A series of analogues of diacylglycerol has been prepared and tested as inhibitors of protein kinase C (PKC). The diketone analogues, 10-hydroxymethyl-8,13-eicosanedione (24), 10-acetoxymethyl-8,13-eicosanedione (25), and 10-methoxymethyl-8,13-eicosa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c56b2266eef7794431b6cd8b36091f3f
https://doi.org/10.1016/0008-6215(92)85036-y
https://doi.org/10.1016/0008-6215(92)85036-y
Autor:
Richard J. K. Taylor, Jackie Hook, Josie C. Briggs, Alan P. Dawson, Alan H. Haines, Ian Gibson
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 2:131-134
A series of conformationally-restricted diacylglycerol analogues have been prepared in homochiral form as potential protein kinase C antagonists using D-ribonolactone and D- and L-2-deoxyribose as starting materials.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c794faf6f285998b5926a573874b5a0
https://doi.org/10.1016/s0960-894x(01)80434-0
https://doi.org/10.1016/s0960-894x(01)80434-0
Autor:
Josie C. Briggs, Richard J. K. Taylor, Alan H. Haines, Silkie Meiners, Alan P. Dawson, Jackie Hook, Alan Lloyd, Ian Gibson
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 2:127-130
Structural analogues of diacylglycerol have been synthesized in an attempt to discover antagonists of protein kinase C with the aim of developing new agents for preventing cell proliferation. Structural analogues of diacylglycerol have been synthesiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce8e20027e6f153852839c78a9de6660
https://doi.org/10.1016/s0960-894x(01)80433-9
https://doi.org/10.1016/s0960-894x(01)80433-9
Publikováno v:
J. Chem. Soc., Chem. Commun.. :1039-1041
2-Chloromethyl-4-nitrophenyl α-D-glucopyranoside, prepared by a novel, four-step route from 2-methylphenyl α-D-glucopyranoside tetraacetate, is highly effective as an enzyme-activated irreversible inhibitor of yeast α-glucosidase and is much super
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3cdd2c80bc6c6f94ed919bdcb619b28
https://doi.org/10.1039/c39920001039
https://doi.org/10.1039/c39920001039