Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ritobroto Sengupta"'
Autor:
Steven M. Weinreb, Ritobroto Sengupta
Publikováno v:
Synthesis. 44:2933-2937
Conjugate addition of a variety of aryl lithiocyanocuprates to nitrosoalkenes generated from α-chloro aldoximes, followed by in situ dehydration of the crude α-aryl aldoxime product with N , N ′-dicyclohexylcarbodiimide, affords α-aryl nitriles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::016296a21519191e5d27bbe3c1991fa5
https://doi.org/10.1055/s-0032-1316984
https://doi.org/10.1055/s-0032-1316984
Publikováno v:
Tetrahedron. 67:8229-8234
Intermolecular Michael-type conjugate additions of some in situ-generated ring-substituted nitrosocyclohexenes with both carbon- and heteronucleophiles have been found to be highly stereoselective, leading predominantly (or exclusively) to products r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4dcb5bdd4c6b4c71edec8e1b956cf9f
https://doi.org/10.1016/j.tet.2011.08.054
https://doi.org/10.1016/j.tet.2011.08.054
Autor:
Ritobroto Sengupta, Steven M. Weinreb
Publikováno v:
ChemInform. 43
Conjugate addition of a variety of aryl lithiocyanocuprates to nitrosoalkenes generated from α-chloro aldoximes, followed by in situ dehydration of the crude α-aryl aldoxime product with N , N ′-dicyclohexylcarbodiimide, affords α-aryl nitriles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bf1f5f843ade93b0321edf2d8d85e64
https://doi.org/10.1002/chin.201252078
https://doi.org/10.1002/chin.201252078