Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jeremy D Pettigrew"'
Autor:
Johanna Richter, Jana Karolova, Yohannes Gebreselassie, Georg Lenz, Chris T. Williamson, Mark S. Cragg, Michael Svaton, Beatriz Valle-Argos, Lindsay D. Smith, Elizabeth Lemm, Nicola J. Weston-Bell, Graham Packham, Laura I. Karydis, Andrew J. Steele, Curtis Harwig, Karel Helman, Freda K. Stevenson, Pavel Klener, Matthew J. Carter, Jennifer Cross, Francesco Forconi, Lloyd F Mackenzie, Jeremy D Pettigrew
Publikováno v:
Clin Cancer Res
Purpose:PI3K signaling is a common feature of B-cell neoplasms, including chronic lymphocytic leukemia (CLL) and diffuse large B-cell lymphoma (DLBCL), and PI3K inhibitors have been introduced into the clinic. However, there remains a clear need to d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e14b2de6e33034fe5f7f6794dee808d8
https://europepmc.org/articles/PMC7124891/
https://europepmc.org/articles/PMC7124891/
Autor:
Jeremy D Pettigrew, Sapna Padania, Ray Cooke, Curtis W. Harwig, Patrick Tam, Lloyd F Mackenzie, Eleanor Barton, Dylan Williams, Judy Toews, Dorothea Scholl
Publikováno v:
Drug Metabolism and Pharmacokinetics. 35:S30-S31
Autor:
Eleanor Barton, Patrick Tam, Iain Shaw, Philip Bond, Curtis W. Harwig, Lloyd F Mackenzie, Sapna Padania, Jeremy D Pettigrew, Ray Cooke, Judy Toews, Dorothea Scholl
Publikováno v:
Drug Metabolism and Pharmacokinetics. 35:S30
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8de2538574a8860ed13fe486503afae2
https://doi.org/10.1002/047084289x.rn00592.pub2
https://doi.org/10.1002/047084289x.rn00592.pub2
Autor:
Leo A. Paquette, Jeremy D. Pettigrew
Publikováno v:
Synthesis. 2009:379-384
Convenient access to polycondensed heterocyclic networks has been realized through exposure of bridged hydroxy acetonides to appropriate reagents.
Autor:
Peter R. Wilson, Jeremy D. Pettigrew
Publikováno v:
The Journal of Organic Chemistry. 71:1620-1625
A series of demethyl analogues of the natural products xyloketal A, B, C, D, and G have been prepared in a notably direct manner from 3-hydroxymethyl-2-methyl-4,5-dihydrofuran and a series of corresponding phenols. These syntheses featured a boron tr
Autor:
Jeremy D. Pettigrew, Charles H. DePuy
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[534-07-6] C3H4Cl2O (MW 126.97) InChI = 1S/C3H4Cl2O/c4-1-3(6)2-5/h1-2H2 InChIKey = SUNMBRGCANLOEG-UHFFFAOYSA-N (starting material for the synthesis of cyclopropanols2 and cyclopropenones3) Alternate Name: 1,3-dichloro-2-propanone. Physical Data: mp 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a06918fea85349595f65ed531b11687
https://doi.org/10.1002/047084289x.rd083.pub2
https://doi.org/10.1002/047084289x.rd083.pub2
Autor:
Peter R. Wilson, Jeremy D. Pettigrew
Publikováno v:
ChemInform. 37
[reaction: see text] The first total synthesis of the C(3)-symmetric and biologically active natural product, (-)-xyloketal A, has been accomplished in one step from phloroglucinol (1,3,5-trihydroxybenzene) and (4R)-3-hydroxymethyl-2,4-dimethyl-4,5-d
Autor:
Jeremy D, Pettigrew, Peter D, Wilson
Publikováno v:
The Journal of organic chemistry. 71(4)
A series of demethyl analogues of the natural products xyloketal A, B, C, D, and G have been prepared in a notably direct manner from 3-hydroxymethyl-2-methyl-4,5-dihydrofuran and a series of corresponding phenols. These syntheses featured a boron tr