14301-29-2Relevant academic research and scientific papers
One-Step Transformation of Trichloroacetamide into Isonitrile
Adachi, Masaatsu,Miyasaka, Tadachika,Hashimoto, Honoka,Nishikawa, Toshio
, p. 380 - 383 (2017)
A one-step transformation of trichloroacetamide, a protective group for the amine function, into isonitrile was successfully developed. The substrate scope and functional group tolerance of this procedure are also described.
N-Acylcatecholamines and 3,4-Dihydro-6,7-isoquinolinediols from N-Acyl-3,4-dimethoxyphenethylamines
Niederstein, Yvonne,Peter, Martin G.
, p. 1189 - 1194 (2007/10/02)
The N-acetamides 2a and 2e are cleaved with boron tribromide to yield as expected the catechols 3a and 3e whereas, under the same conditions, mixtures of the catechols 3b, 3c, 3f, or 3g and 1-(haloalkyl)dihydroisoquinolines 4
