Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Henri Piras"'
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10f3b5fae19dab92aedc1e7b63753f33
https://doi.org/10.1002/0471264229.os096.22
https://doi.org/10.1002/0471264229.os096.22
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb1140187e227e969b07c001c2129418
https://doi.org/10.1002/0471264229.os095.22
https://doi.org/10.1002/0471264229.os095.22
Publikováno v:
ACS Catalysis. 6:1109-1112
A photochemical (UVA) continuous flow process for the amination of thioethers and sulfoxides was performed with trichloroethoxysulfonyl azide in the presence of catalytic iron(III) acetylacetonate. Aromatic and aliphatic sulfilimines and sulfoximines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de6c9e8a11fe31b6f21278a299d7aa4c
https://doi.org/10.1021/acscatal.5b02495
https://doi.org/10.1021/acscatal.5b02495
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ab8d475e6743b8c8d8e980775d74a91
https://doi.org/10.1002/0471264229.os094.11
https://doi.org/10.1002/0471264229.os094.11
Publikováno v:
Israel Journal of Chemistry. 53:923-931
Mild conditions for the gold-catalyzed dehydrative cyclization of carbamate-protected azaallylic alcohols to form saturated nitrogen heterocycles are reported. The cyclization reactions are high-yielding, operationally easy to perform, and provide he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83cc5233611333bac2db54b0ad86f952
https://doi.org/10.1002/ijch.201300041
https://doi.org/10.1002/ijch.201300041
Autor:
Henri Piras, Hélène Lebel
Publikováno v:
ChemInform. 46
The synthesis of a variety of chiral sulfilimines and sulfoximines is described. The amination of thioethers with a chiral N-mesyloxycarbamate was achieved in high yields and stereoselectivities using Rh2[(S)-nttl]4 as catalyst in the presence of 4-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6536427dbe87919be279aad294b226f5
https://doi.org/10.1002/chin.201533118
https://doi.org/10.1002/chin.201533118
Autor:
Henri Piras, Hélène Lebel
Publikováno v:
The Journal of organic chemistry. 80(7)
The synthesis of a variety of chiral sulfilimines and sulfoximines is described. The amination of thioethers with a chiral N-mesyloxycarbamate was achieved in high yields and stereoselectivities using Rh2[(S)-nttl]4 as catalyst in the presence of 4-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7318752a1ceb8a2a64011cf20a11b6a8
https://pubmed.ncbi.nlm.nih.gov/25751154
https://pubmed.ncbi.nlm.nih.gov/25751154
Publikováno v:
ChemInform. 45
Chiral sulfilimines are prepared by rhodium-catalyzed intermolecular amination of thioethers with the readily available N-mesyloxycarbamate (I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29927dc4fcbb2221dbbc03fb7f66b854
https://doi.org/10.1002/chin.201451100
https://doi.org/10.1002/chin.201451100
Publikováno v:
Angewandte Chemie (International ed. in English). 53(28)
A stereoselective Rh-catalyzed intermolecular amination of thioethers using a readily available chiral N-mesyloxycarbamate to produce sulfilimines in excellent yields and diastereomeric ratio is described. A catalytic mixture of 4-dimethylaminopyridi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98e32bad0ab18049ef89a225370d1101
https://pubmed.ncbi.nlm.nih.gov/24888544
https://pubmed.ncbi.nlm.nih.gov/24888544