Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Landry, Serge"'
Autor:
Landry, Serge R.
Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.
Externí odkaz:
http://hdl.handle.net/1866/29200
Autor:
Landry, Serge
Th. doct.-ing.--Chim. moléculaire--Grenoble 1, 1987.
Externí odkaz:
http://catalogue.bnf.fr/ark:/12148/cb376069547
Autor:
Fader, Lee D., Landry, Serge, Morin, Sébastien, Kawai, Stephen H., Bousquet, Yves, Hucke, Oliver, Goudreau, Nathalie, Lemke, Christopher T., Bonneau, Pierre, Titolo, Steve, Mason, Stephen, Simoneau, Bruno
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1 June 2013 23(11):3396-3400
Autor:
Fader, Lee D., Landry, Serge, Goulet, Sylvie, Morin, Sébastien, Kawai, Stephen H., Bousquet, Yves, Dion, Isabelle, Hucke, Oliver, Goudreau, Nathalie, Lemke, Christopher T., Rancourt, Jean, Bonneau, Pierre, Titolo, Steve, Amad, Ma’an, Garneau, Michel, Duan, Jianmin, Mason, Stephen, Simoneau, Bruno
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1 June 2013 23(11):3401-3405
Autor:
Isabelle Duchesne, Christian Brochu, Claude Y. Legault, Anne-Marie Faucher, Andrew Myles, Susanne Hantos, Landry Serge, Amélie Roy
Publikováno v:
Tetrahedron Letters. 39:8425-8428
Lithium tri- n -butyl borohydride showed high selectivity in the reduction of α- and β-oxygenated ketones, giving a preponderance of the chelation controlled products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454cfcd9ceb7e55643f25d9fb809cb1b
https://doi.org/10.1016/s0040-4039(98)01883-8
https://doi.org/10.1016/s0040-4039(98)01883-8
Publikováno v:
The Journal of Organic Chemistry. 62:9276-9283
To enhance the diastereoselectivity of the hydrogen transfer reaction of acyclic substrates bearing 1,2- or 1,3-diols, the feasibility of a strategy employing bifunctional protecting groups has been demonstrated. This strategy is based upon the “ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34cc287ae0c7fd50ae4d18188e9dd5c0
https://doi.org/10.1021/jo971595s
https://doi.org/10.1021/jo971595s
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
ChemInform. 29
To enhance the diastereoselectivity of the hydrogen transfer reaction of acyclic substrates bearing 1,2- or 1,3-diols, the feasibility of a strategy employing bifunctional protecting groups has been demonstrated. This strategy is based upon the “ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::083b965208d3d9294ab60fbdf95bc8db
https://doi.org/10.1002/chin.199820052
https://doi.org/10.1002/chin.199820052
Autor:
Anne-Marie Faucher, Isabelle Duchesne, Christian Brochu, Susanne Hantos, Andrew Myles, Landry Serge, Amélie Roy, Claude Y. Legault
Publikováno v:
ChemInform. 30
Lithium tri- n -butyl borohydride showed high selectivity in the reduction of α- and β-oxygenated ketones, giving a preponderance of the chelation controlled products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7190644fd56e857f4289da6e5987b75d
https://doi.org/10.1002/chin.199905076
https://doi.org/10.1002/chin.199905076
Autor:
Fader, Lee D., Bethell, Richard, Bonneau, Pierre, Bös, Michael, Bousquet, Yves, Cordingley, Michael G., Coulombe, René, Deroy, Patrick, Faucher, Anne-Marie, Gagnon, Alexandre, Goudreau, Nathalie, Grand-Maître, Chantal, Guse, Ingrid, Hucke, Oliver, Kawai, Stephen H., Lacoste, Jean-Eric, Landry, Serge, Lemke, Christopher T., Malenfant, Eric, Mason, Stephen, Morin, Sébastien, O’Meara, Jeff, Simoneau, Bruno, Titolo, Steve, Yoakim, Christiane
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 1 January 2011 21(1):398-404