Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Jean-François Brazeau"'
Un cowboy éploré. Un musicien confus. Un scientifique ignoré. Une policière à bout de souffle. Des pères désespérés. Un super-héros déchu. Six récits qui illustrent quelques facettes de la relation complexe que l'humain entretient avec la
Publikováno v:
Journal of the American Chemical Society. 134:2742-2749
The discovery of complementary methods for enantioselective transition metal-catalyzed cyclization with silyloxyenynes has been accomplished using chiral phosphine ligands. Under palladium catalysis, 1,6-silyloxyenynes bearing a terminal alkyne led t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::740331741f5851f23c9371defac04f2f
https://doi.org/10.1021/ja210388g
https://doi.org/10.1021/ja210388g
Autor:
François Godin, Yvan Guindon, Jean-François Brazeau, Ioannis Katsoulis, Isabelle Fontaine, Philippe Mochirian
Publikováno v:
The Journal of Organic Chemistry. 76:7654-7676
The structure-activity study of a bioactive natural product containing polypropionate subunits requires that its stereoisomers also be evaluated. Therefore, a general approach to synthesize these motifs is necessary. We describe herein the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6df7c102d7dbb9fefa566e87c4843f8
https://doi.org/10.1021/jo2013884
https://doi.org/10.1021/jo2013884
Publikováno v:
Current Organic Chemistry. 10:1939-1961
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1bf3538d477c5227ba5f83cbf13b42b
https://doi.org/10.2174/138527206778521259
https://doi.org/10.2174/138527206778521259
Autor:
Serge I. Gorelsky, Yvan Guindon, François Godin, Michel Prévost, Jean-François Brazeau, Philippe Mochirian, Frédérick Viens
Publikováno v:
The Journal of organic chemistry. 78(12)
Exocyclic radical reductions were thoroughly investigated in the context of the synthesis of polysubstituted tetrahydropyrans, which are found in numerous macrolides. The radical precursors studied herein were generated by tandem cycloetherification
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb1847e21992a631e0fb68adcf7eaf5f
https://pubmed.ncbi.nlm.nih.gov/23688058
https://pubmed.ncbi.nlm.nih.gov/23688058
Publikováno v:
ChemInform. 43
Novel asymmetric 5-exo-dig and 5-endo-dig cyclizations of silyloxyenynes using palladium and gold complexes are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bce74410c2bb55d7a7c318436308b694
https://doi.org/10.1002/chin.201233057
https://doi.org/10.1002/chin.201233057
Publikováno v:
ChemInform. 42
During continuing studies with a novel oxidative gold oxyarylation reaction, arylsilanes were found to be competent coupling partners, providing further evidence for an intramolecular electrophilic aromatic substitution mechanism. While providing yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c71c8562411c688ec0ee9760ed0e7cbf
https://doi.org/10.1002/chin.201108040
https://doi.org/10.1002/chin.201108040
Publikováno v:
Organic letters. 12(21)
During continuing studies with a novel oxidative gold oxyarylation reaction, arylsilanes were found to be competent coupling partners, providing further evidence for an intramolecular electrophilic aromatic substitution mechanism. While providing yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b4f4349d4120822456e668fbba693da
https://pubmed.ncbi.nlm.nih.gov/21028911
https://pubmed.ncbi.nlm.nih.gov/21028911
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8078fb2722b85a79b22b1ebe15d852a4
https://doi.org/10.1002/chin.200726236
https://doi.org/10.1002/chin.200726236
Autor:
Yvan Guindon, Jean-François Brazeau
Publikováno v:
Organic letters. 6(15)
[reaction: see text] Reported herein is the synthesis of 8 out of 16 polypropionates derived from our propionate units. A new strategy involving a stereoselective Mukaiyama aldol reaction followed by a stereoselective free-radical-based hydrogen tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09eecf3023acf97f5288ef72dd54ed6f
https://pubmed.ncbi.nlm.nih.gov/15255700
https://pubmed.ncbi.nlm.nih.gov/15255700