Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Andrew N. Payne"'
Autor:
Peter Nash, Stephen Hall, Johan Vanhoof, Rita Tarzynski-Potempa, Udayasankar Arulmani, Alfred Cividino, Kristina Unnebrink, Andrew N. Payne
Publikováno v:
Rheumatology and Therapy
Introduction Adalimumab, an anti-tumor necrosis factor antibody, is currently available in a 40 mg/0.8 mL formulation. The objective of this analysis was to evaluate injection site-related pain, safety, and tolerability of a 40 mg/0.4 mL formulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::120bb5ffae790a52d158ba677c6c33f8
https://pubmed.ncbi.nlm.nih.gov/27747583
https://pubmed.ncbi.nlm.nih.gov/27747583
Autor:
Andrew N. Payne, Andrew B. Holmes, Craig L. Francis, Neil Roy Curtis, Jonathan W. Burton, Miles S. Congreve, S. Y. Frankie Mak
Publikováno v:
Synthesis. :3199-3201
A synthesis of the halogenated medium-ring ether natural product (+)-obtusenyne is reported utilizing a Claisen rearrangement and an intramolecular hydrosilation as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::173b686cb74f8e79a76d22c10953f27c
https://doi.org/10.1055/s-2005-918470
https://doi.org/10.1055/s-2005-918470
Autor:
Andrew N. Payne, Stanley M. Roberts
Publikováno v:
ChemInform. 24
The 6′-fluorocarbocyclic nucleosides 1 and 2 have been synthesized from the bicyclic ketone 3 in 16 and 2% yield respectively. The nucleoside 1 has been incorporated into short chains of DNA using an automated synthesizer and these oligonucleotides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27e098f93086449d0ae4a4f089562e5c
https://doi.org/10.1002/chin.199306297
https://doi.org/10.1002/chin.199306297
Autor:
Andrew N. Payne, Mary Ann M. Fuhry, Simon E. Ward, Miles S. Congreve, R. A. Robinson, Andrew B. Holmes, Edwin C. Davison
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fd882711db314d6de9ffa750c7d1d3f
https://doi.org/10.1002/chin.199406101
https://doi.org/10.1002/chin.199406101
Publikováno v:
ChemInform. 28
A convenient preparation of α-halo enamines using oxalyl halides is described together with applications of these reagents in the halogenation of β-hydroxy cyclic ethers and lactones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3a13e973025e63b80e5c5ce47668495
https://doi.org/10.1002/chin.199741080
https://doi.org/10.1002/chin.199741080
Autor:
Stanley M. Roberts, Andrew N. Payne
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2633-2641
The 6′-fluorocarbocyclic nucleosides 1 and 2 have been synthesized from the bicyclic ketone 3 in 16 and 2% yield respectively. The nucleoside 1 has been incorporated into short chains of DNA using an automated synthesizer and these oligonucleotides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae8e9031fc37eddb0ca5ead6a9cd1ecf
https://doi.org/10.1039/p19920002633
https://doi.org/10.1039/p19920002633
Autor:
Sofia I. Pascu, Andrew B. Holmes, Andrew N. Payne, Andrew J. Wildsmith, Miles Congreve, Craig L. Francis, Neil Roy Curtis, S. Y. Frankie Mak, Jonathan W. Burton, John E. Davies
Publikováno v:
ChemInform. 39
An enantioselective synthesis of the halogenated medium-ring ether natural product (+)-obtusenyne is reported which uses the ring expansion of a seven-membered ketene acetal by means of a Claisen rearrangement to construct the core nine-membered oxyg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa6f6bd1a1c99eb1f699d8cce05e1311
https://doi.org/10.1002/chin.200833203
https://doi.org/10.1002/chin.200833203
Autor:
Andrew N. Payne, John E. Davies, Craig L. Francis, Sofia I. Pascu, Neil Roy Curtis, S. Y. Frankie Mak, Andrew B. Holmes, Miles Congreve, Andrew J. Wildsmith, Jonathan W. Burton
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 14(9)
An enantioselective synthesis of the halogenated medium-ring ether natural product (+)-obtusenyne is reported which uses the ring expansion of a seven-membered ketene acetal by means of a Claisen rearrangement to construct the core nine-membered oxyg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77eafb4397fc276ac3d24fd467f177a
http://ora.ox.ac.uk/objects/uuid:e77c401b-8833-46f5-b9dc-0093b2c598a9
http://ora.ox.ac.uk/objects/uuid:e77c401b-8833-46f5-b9dc-0093b2c598a9
Publikováno v:
Chemical Communications. :1067-1068
A convenient preparation of α-halo enamines using oxalyl halides is described together with applications of these reagents in the halogenation of β-hydroxy cyclic ethers and lactones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b74efc695f330a0a3edff7c9407223d0
https://doi.org/10.1039/a701999h
https://doi.org/10.1039/a701999h