Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Bruno Anxionnat"'
Autor:
Bruno Anxionnat, Benoit Robert, Pascal George, Gino Ricci, Marc-Antoine Perrin, Domingo Gomez Pardo, Janine Cossy
Publikováno v:
The Journal of Organic Chemistry. 79:5935-5938
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83f5cbc7a0bbf37096b7aadd0176a241
https://doi.org/10.1021/jo501209b
https://doi.org/10.1021/jo501209b
Publikováno v:
Organic Letters. 15:3876-3879
An iridium-catalyzed hydrogen transfer has been developed in the presence of p-benzoquinone, allowing the synthesis of a diversity of substituted benzofurans, benzothiophenes, and indoles from substituted benzylic alcohols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd72d3fb7537ee7e816cb2c3f8381878
https://doi.org/10.1021/ol401610e
https://doi.org/10.1021/ol401610e
Publikováno v:
European Journal of Organic Chemistry. 2012:4453-4456
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e5efcc480033b82e726dcfd7fc380be
https://doi.org/10.1002/ejoc.201200850
https://doi.org/10.1002/ejoc.201200850
Publikováno v:
Organic Letters. 13:4084-4087
The monoalkylation of acetonitrile by primary alcohols was achieved in a one-pot sequence in the presence of iridium catalysts. A diversity of nitriles has been obtained from aryl- and alkyl-methanols in excellent yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc68ecc2e9d4e4ce8322af5b83fc6656
https://doi.org/10.1021/ol2015972
https://doi.org/10.1021/ol2015972
Publikováno v:
Tetrahedron Letters. 50:3470-3473
A safe and inexpensive synthesis of amides, from benzylic alcohols and nitriles and from t-butyl acetate and nitriles, using a Ritter reaction catalyzed by FeCl3·6H2O is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b19af29b807cb4b0c876b46dff0d47a7
https://doi.org/10.1016/j.tetlet.2009.02.208
https://doi.org/10.1016/j.tetlet.2009.02.208
Publikováno v:
ChemInform. 44
An iridium-catalyzed hydrogen transfer has been developed in the presence of p-benzoquinone, allowing the synthesis of a diversity of substituted benzofurans, benzothiophenes, and indoles from substituted benzylic alcohols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cadbfeaba1d0b466149bca05dc63f6bc
https://doi.org/10.1002/chin.201351126
https://doi.org/10.1002/chin.201351126
Publikováno v:
ChemInform. 44
The first iridium-catalyzed intramolecular alkylation ofnitriles with primary and secondary alcohols through hydrogen transfer is described. This reaction allows access to precursors of biologically active arylmethylamines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::526fac1caf5e490ed1c79d71b1c4c01e
https://doi.org/10.1002/chin.201308030
https://doi.org/10.1002/chin.201308030
Autor:
Janine Cossy, Pascal George, Domingo Gomez Pardo, Benoît Robert, Marc-Antoine Perrin, Gino Ricci, Bruno Anxionnat
Publikováno v:
ChemInform. 43
The ring expansion of 2-hydroxymethyl azetidines and prolinols proceeds with high enantioselectivity for small rings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0e22002ab3f82945c6af9f7240ceba3
https://doi.org/10.1002/chin.201249153
https://doi.org/10.1002/chin.201249153
Autor:
Benoît Robert, Bruno Anxionnat, Janine Cossy, Pascal George, Marc-Antoine Perrin, Domingo Gomez Pardo, Gino Ricci
Publikováno v:
The Journal of organic chemistry. 77(14)
As the replacement of a hydrogen atom by a fluorine atom in a compound can have an important impact on its biological properties, the development of methods allowing the introduction of a fluorine atom is of great importance. The scope and limitation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64a0d380bc411b11fae5a739210aeb5a
https://pubmed.ncbi.nlm.nih.gov/22686336
https://pubmed.ncbi.nlm.nih.gov/22686336
Publikováno v:
ChemInform. 42
The monoalkylation of acetonitrile by primary alcohols was achieved in a one-pot sequence in the presence of iridium catalysts. A diversity of nitriles has been obtained from aryl- and alkyl-methanols in excellent yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5417e3a2e6028f68b5e32b3df0eaa050
https://doi.org/10.1002/chin.201149078
https://doi.org/10.1002/chin.201149078