Zobrazeno 1 - 10
of 15
pro vyhledávání: '"John B. J. Pavey"'
Autor:
Miles N. Tackett, John B. J. Pavey, Kieron E. Wesson, David Osborn, Maria A. Palomero, Masakuni Kori, Michael C. Willis, James S. Scott, Jag Paul Heer, Matthew L. Maddess, James C. Anderson, Hidenori Watanabe, Paul Brennan, Michael W. Cappi, Catherine Pinel, Joanne Norman, Céline Helgen, Jiirgen Schnaubelt, Stephen P. Marsden, Lesley A. Robinson, Christopher D. Spilling, Steven V. Ley, Cyrille Kouklovsky
For over 30 years, rapamycin has generated a sustained and intense interest from the scientific community as a result of its exceptional pharmacological properties and challenging structural features. In addition to its well known therapeutic value a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54706266323cc943ab83a92c095d5f77
https://ora.ox.ac.uk/objects/uuid:001f9546-a1be-4c4e-985b-5e92b3d0916f
https://ora.ox.ac.uk/objects/uuid:001f9546-a1be-4c4e-985b-5e92b3d0916f
Publikováno v:
Org. Biomol. Chem.. 2:869-875
The 5'-triphosphates of 2'-hydroxymethyluridine (2'-homouridine) and 2'-hydroxyethyluridine were prepared from the corresponding acetyl-protected nucleosides by initial phosphitylation with 2-chloro-5,6-benzo-1,2,3-dioxaphosphorin-4-one. 2'-Acetamido
Publikováno v:
Tetrahedron Letters. 39:6967-6970
An efficient route to 2′-homouridine ( 1 ), a new nucleoside analogue, is reported that is based on an ene reaction. This nucleoside has been incorporated into a dinucleoside monophosphate and hydrolytic studies on the dimer show that it does not b
Autor:
Holger Eick, Alexander C. Humphries, Andrew R. Ross, John B. J. Pavey, Richard J. Boyce, Steven V. Ley, Jörg Pietruszka, Robert Downham
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :3907-3912
The total synthesis of the protein phosphatase inhibitor okadaic acid 1 is reported using a convergent coupling strategy of three components, all of which may be prepared using chemistry developed in our laboratories.
Publikováno v:
Nucleosides and Nucleotides. 16:1497-1501
Five 2′-C-functionalized nucleosides (1–5) have been prepared and incorporated into dinucleoside monophosphates. The effect of the functionality on the stability of the adjacent phosphodiester bond toward hydrolysis by nuclease enzymes and extrem
Autor:
Julie Fisher, Mai-Yee Chan, Stephen Paul Collingwood, Robin Alec Fairhurst, John B. J. Pavey, Richard Cosstick, Anthony J. Lawrence, Ian A. O'Neil
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2761-2768
Uridine 2′-C-3′-O-γ-butyrolactone 5a has been prepared by cyclisation of 2′-α-C-carboxymethyl-2′-deoxyuridine 8 in acetic acid–methanol. Detailed 1H NMR studies on compound 5a clearly demonstrate cis fusion between the γ-lactone and the
Publikováno v:
The Journal of Organic Chemistry. 61:9213-9222
Four functionalized 2‘-deoxy-2‘-α-C-branched nucleosides, namely, 2‘-deoxy-2‘-α-C-(carboxymethyl)uridine, 2‘-deoxy-2‘-α-C-acetamidouridine, 2‘-deoxy-2‘-α-C-(hydroxyethyl)uridine, and 2‘-deoxy-2‘-α-...
Publikováno v:
ChemInform. 26
Publikováno v:
ChemInform. 28
Four functionalized 2‘-deoxy-2‘-α-C-branched nucleosides, namely, 2‘-deoxy-2‘-α-C-(carboxymethyl)uridine, 2‘-deoxy-2‘-α-C-acetamidouridine, 2‘-deoxy-2‘-α-C-(hydroxyethyl)uridine, and 2‘-deoxy-2‘-α-...
Autor:
R. A. Fairhurst, John Fisher, Richard Cosstick, S. P. Collingwood, John B. J. Pavey, Mai-Yee Chan, Ian A. O'Neil, Anthony J. Lawrence
Publikováno v:
ChemInform. 29