Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Martin, Pouliot"'
Autor:
Christopher M. Baker, Rob Carson, Matthew Brian Hotson, Jim Harrison, David Gravestock, Martin Pouliot, Konstantinos Papachristos, Alan John Dowling, Nathan J. Kidley
Publikováno v:
Journal of chemical information and modeling. 60(8)
Databases of small, potentially bioactive molecules are ubiquitous across the industry and academia. Designed such that each unique compound should appear only once, the multiplicity of ways in which many compounds can be represented means that these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78de4cd967f892f9f2e08c8206f8003d
https://pubmed.ncbi.nlm.nih.gov/32644790
https://pubmed.ncbi.nlm.nih.gov/32644790
Publikováno v:
Bioorganic & Medicinal Chemistry. 39:116162
In this review, the synthesis of 33 agrochemicals that received an international standardization organization (ISO) name between January 2015 and December 2018 is described. The aim is to showcase the broad range and scope of reactions, reagents and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::766b50c52ae30e27046e41427fa80a6f
https://doi.org/10.1016/j.bmc.2021.116162
https://doi.org/10.1016/j.bmc.2021.116162
Publikováno v:
Bioorganic & Medicinal Chemistry. 24:317-341
In this review, the synthesis of 30 agrochemicals that received an international standardization organization (ISO) name during the last five years (January 2010 to December 2014) is described. The aim is to showcase the range and scope of chemistrie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6515d7f976f6891481a16515e10f8560
https://doi.org/10.1016/j.bmc.2015.12.014
https://doi.org/10.1016/j.bmc.2015.12.014
Autor:
Stephane Jeanmart, Martin Pouliot
Publikováno v:
Journal of Medicinal Chemistry. 59:497-503
Every week, articles disclosing new antifungal leads reported as promising starting points for optimization projects are published. In many cases, the mechanism that accounts for their antifungal activity has not been fully elucidated. More significa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0bbac6f0c7c8f33aa4026fc87b57959
https://doi.org/10.1021/acs.jmedchem.5b00361
https://doi.org/10.1021/acs.jmedchem.5b00361
Publikováno v:
Angewandte Chemie International Edition. 48:6037-6040
Keywords: alkoxyamines ; boron enolates ; enolyl radicals ; nitroxides ; oxidation ; Free-Radical Polymerization ; Asymmetric Conjugate Addition ; Aldol Reactions ; Grignard-Reagents ; Alkoxyamines ; Cyclizations ; Chemistry ; Nitroxyl ; Isomerizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f020919e1c25588d1f24990d94282623
https://doi.org/10.1002/anie.200902242
https://doi.org/10.1002/anie.200902242
Publikováno v:
Angewandte Chemie. 121:6153-6156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35ac44187b740a9fbd9138e2def3207c
https://doi.org/10.1002/ange.200902242
https://doi.org/10.1002/ange.200902242
Autor:
Martin, Pouliot, Stephane, Jeanmart
Publikováno v:
Journal of medicinal chemistry. 59(2)
Every week, articles disclosing new antifungal leads reported as promising starting points for optimization projects are published. In many cases, the mechanism that accounts for their antifungal activity has not been fully elucidated. More significa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d12c53956117b9e1db23b887f47bdd42
https://pubmed.ncbi.nlm.nih.gov/26313340
https://pubmed.ncbi.nlm.nih.gov/26313340
Publikováno v:
Organic Letters. 8:3597-3599
[reaction: see text] The first synthesis of (-)-panacene has been accomplished in concise, highly stereoselective fashion from commercially available 2-methoxy-6-methylbenzoic acid (15 steps, 8.3% overall yield). The synthesis unambiguously establish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8006f3b58d0d904c90a99d7667de88e3
https://doi.org/10.1021/ol061385e
https://doi.org/10.1021/ol061385e
Autor:
John Boukouvalas, Martin Pouliot
Publikováno v:
Synlett. :343-345
The first synthesis of cadiolide B has been achieved in 6 steps and 42% overall yield from 4-bromo-2(5H)-furanone. The pathway involves sequential, regiocontrolled introduction of the three furanone substituents by means of aldol reactions and Suzuki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3b8d911ea3dded664288bb953a5e9a3
https://doi.org/10.1055/s-2004-837220
https://doi.org/10.1055/s-2004-837220
Publikováno v:
ChemInform. 43
A variety of acyclic and cyclic ketones react with TEMPO in the presence of chlorocatecholborane CBC and TMP as bulky pyridine base to give the α-aminoxylated products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd6151b9051c1ef0ce8973deb1d924c6
https://doi.org/10.1002/chin.201252131
https://doi.org/10.1002/chin.201252131