Chemoselective Hydrogenation Reaction of Unsaturated Bonds in the Presence of an o-Nitrobenzenesulfonyl Group
摘要:
Chemoselective hydrogenation of unsaturated compounds bearing an o-nitrobenzenesulfonyl (Ns)-amide moiety, affording the corresponding saturated compounds, was accomplished efficiently without loss of the nitro group by using the Pd/MS3A catalyst and a H-2 balloon. Partial hydrogenation of alkynes bearing an Ns group to corresponding cis alkenes was achieved with the combination of the Pd/BN catalyst and an additive (diethylenetriamine or acetic acid).
Demeny, Recueil des Travaux Chimiques des Pays-Bas, 1929, vol. 48, p. 1152,1153
作者:Demeny
DOI:——
日期:——
Chemoselective Hydrogenation Reaction of Unsaturated Bonds in the Presence of an <i>o</i>-Nitrobenzenesulfonyl Group
作者:Akinori Kawanishi、Chiyako Miyamoto、Yuki Yabe、Makoto Inai、Tomohiro Asakawa、Yoshitaka Hamashima、Hironao Sajiki、Toshiyuki Kan
DOI:10.1021/ol4002448
日期:2013.3.15
Chemoselective hydrogenation of unsaturated compounds bearing an o-nitrobenzenesulfonyl (Ns)-amide moiety, affording the corresponding saturated compounds, was accomplished efficiently without loss of the nitro group by using the Pd/MS3A catalyst and a H-2 balloon. Partial hydrogenation of alkynes bearing an Ns group to corresponding cis alkenes was achieved with the combination of the Pd/BN catalyst and an additive (diethylenetriamine or acetic acid).