Catalytic Hydrogenation of Amides to Amines under Mild Conditions
作者:Mario Stein、Bernhard Breit
DOI:10.1002/anie.201207803
日期:2013.2.18
Under (not so much) pressure: A general method for the hydrogenation of tertiary and secondary amides to amines with excellent selectivity using a bimetallic Pd–Re catalyst has been developed. The reaction proceeds under low pressure and comparatively low temperature. This method provides organic chemists with a simple and reliable tool for the synthesis of amines.
Tungsten-Catalyzed Transamidation of Tertiary Alkyl Amides
作者:Fang-Fang Feng、Xuan-Yu Liu、Chi Wai Cheung、Jun-An Ma
DOI:10.1021/acscatal.1c01840
日期:2021.6.18
chloride as a catalyst and chlorotrimethylsilane as an additive. The highly electrophilic and oxophilic tungsten catalyst enables the selective scission of a C–N bond of tertiary alkyl amides to effect transamidation of a myriad of structurally and electronically diverse tertiary alkyl amides and amines. Mechanistic study implies that the synergistic effect of the catalyst and the additive could pronouncedly
[reaction: see text] Reaction of carbamoyl chlorides with cyano-Gilman cuprates affords tertiary amides in good to excellent yields. The reaction is general due to the possibility of using reagents made either from organolithium or from Grignard compounds. The characterization of the main side products allowed for the suggestion of a possible mechanism.
Nucleophilic Aminoalkylation with Thiopivalamides1
硫代戊酰胺的亲核氨基烷基化1
3,4-DISUBSTITUTED 3-CYCLOBUTENE-1,2-DIONES AND USE THEREOF
申请人:ALLERGAN, INC.
公开号:US20190047947A1
公开(公告)日:2019-02-14
Described herein are compounds, or pharmaceutically acceptable salts thereof, of the following formula:
The compounds are useful for treating inflammatory and autoimmune diseases.