Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Gilles Berthiaume"'
Autor:
Nadia Fortin, Carl Saint-Louis, Annick Landry, René Gagnon, Gilles Olsen, Sylvain Bernard, Patrick Bherer, Eric Marsault, Véronique Plourde, Gilles Berthiaume, Martin Brassard, Robert Deziel, Axel Mathieu, Gérald Villeneuve, Xiaowen Peng, Hamid R. Hoveyda, Mark Peterson, Graeme L. Fraser, François Bilodeau, Ruoxi Lan, Shridhar Bhat, Annie Doucet, Maude Gauthier, Yves L. Dory, David Lonergan, Shigui Li, Sylvie Beaubien, Luc Ouellet, Pierre Deslongchamps, Alexandre Drouin, Fabrice Galaud, Sophie Beauchemin, Manon Champagne, Kamel Benakli, Mahesh Ramaseshan, Laurence Foucher, Jean François Pinault, Martin Vezina, Daniel Fortin, Zhigang Wang
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:4731-4735
A new method for solid phase parallel synthesis of chemically and conformationally diverse macrocyclic peptidomimetics is reported. A key feature of the method is access to broad chemical and conformational diversity. Synthesis and mechanistic studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf941f5cc5a05130451a2464ff661573
https://doi.org/10.1016/j.bmcl.2008.06.085
https://doi.org/10.1016/j.bmcl.2008.06.085
Publikováno v:
European Journal of Organic Chemistry. 2006:3681-3686
The synthesis of a completely substituted ring A of Taxol is reported and it is shown that the C13-OP group must have a β configuration to succeed in the formation of 12-membered rings, a requisite for the construction of the B and C rings of Taxol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8e9795e072c5c44121dccb8338c1177
https://doi.org/10.1002/ejoc.200600284
https://doi.org/10.1002/ejoc.200600284
Autor:
Gilles Berthiaume
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
(1; R = Me) [52784-37-9] C8H10O3 (MW 154.18) InChI = 1S/C8H10O3/c1-11-8(10)6-4-2-3-5-7(6)9/h4H,2-3,5H2,1H3 InChIKey = CJTBWDJSTLSONF-UHFFFAOYSA-N (2; R = Et) [57205-09-1] C9H12O3 (MW 168.21) InChI = 1S/C9H12O3/c1-2-12-9(11)7-5-3-4-6-8(7)10/h5H,2-4,6H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a9cf07774c978fa70278825da99d0f3
https://doi.org/10.1002/047084289x.rm222
https://doi.org/10.1002/047084289x.rm222
Autor:
Gilles Berthiaume
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
(1; R = tert-Bu) [132117-94-3] C10H16O3 (MW 184.23) InChI = 1S/C10H16O3/c1-5-6-8(11)7-9(12)13-10(2,3)4/h5-6H,7H2,1-4H3/b6-5+ InChIKey = YBQWHQCHKADBAN-AATRIKPKSA-N (2; R = Et) [25654-09-5] C8H12O3 (MW 156.18) InChI = 1S/C8H12O3/c1-3-5-7(9)6-8(10)11-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6c3333ec1fb3c6e1d88a381f345cf53
https://doi.org/10.1002/047084289x.rb405
https://doi.org/10.1002/047084289x.rb405
Publikováno v:
Tetrahedron Letters. 27:5451-5454
A study on the base-catalyzed intramolecular Michael addition of cyclic β-ketoester enones 9 and 10 (n = 0-3, R 1 = R 2 = H and/or CH 3 ) is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::563b76162be14d235cb05579adf2ccd9
https://doi.org/10.1016/s0040-4039(00)85235-1
https://doi.org/10.1016/s0040-4039(00)85235-1
Publikováno v:
Tetrahedron Letters. 27:5455-5458
A study on the base-catalyzed intramolecular Michael addition of β-ketoester-ynone 1 (n′ = 1–2, n = 0–3) is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f3c1e3bfabbc3ce68fab58ba3815ade
https://doi.org/10.1016/s0040-4039(00)85236-3
https://doi.org/10.1016/s0040-4039(00)85236-3
Autor:
Gilles Berthiaume
Publikováno v:
Proceedings of the American Mathematical Society. 66:335-343
Quasi-uniformities in spaces of subsets are investigated. It is shown, by means of examples, how quasi-uniformities can play a unifying role in the study of topological structures in hyperspaces. The main application is the following result: an infin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::452f3a570c710891cfa5e64b909b94d1
https://doi.org/10.1090/s0002-9939-1977-0482620-9
https://doi.org/10.1090/s0002-9939-1977-0482620-9
Publikováno v:
ChemInform. 18
A study on the base-catalyzed intramolecular Michael addition of β-ketoester-ynone 1 (n′ = 1–2, n = 0–3) is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44a7b088026c6a5927fbc48d8d7b486d
https://doi.org/10.1002/chin.198715104
https://doi.org/10.1002/chin.198715104
Publikováno v:
ChemInform. 18
A study on the base-catalyzed intramolecular Michael addition of cyclic β-ketoester enones 9 and 10 (n = 0-3, R 1 = R 2 = H and/or CH 3 ) is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f097decae5456ffe96f54d0b8f2aa00a
https://doi.org/10.1002/chin.198715105
https://doi.org/10.1002/chin.198715105