106053-24-1Relevant articles and documents
Syntheses of chiral 1,3-disubstituted tetrahydro-β-carbolines via CIAT process: highly stereoselective Pictet-Spengler reaction of d-tryptophan ester hydrochlorides with various aldehydes
Xiao, Sen,Lu, Xia,Shi, Xiao-Xin,Sun, Yu,Liang, Li-Li,Yu, Xin-Hong,Dong, Jing
experimental part, p. 430 - 439 (2009/09/06)
A highly stereoselective Pictet-Spengler reaction of d-tryptophan methyl ester hydrochloride 1-HCl with various aldehydes via a CIAT (crystallization-induced asymmetric transformation) process is described. It was revealed that the CIAT process should be
Syntheses og Stilbenes with a C2-Sidechain in o-Position and of their Deuteriated Analogues
Mayer, Klaus K.,Prior, Silvia,Wiegrebe, Wolfgang
, p. 511 - 532 (2007/10/02)
Syntheses of o-(β-aminoethyl)-stilbene-urethanes (types 1, 2 and 3) and o-(β-phenethyl)-stilbenes 4 are described.The urethanes are obtained by degradation of 1-benzyl-1,2,3,4-tetrahydroisoquinolines with ethylchloroformate; 4 is synthesized by reduction of desoxybenzoines, followed by o-formylation and Wittig-reaction.The deuteriated isotopomers were obtained via the corresponding deuteriated precursors. - Keywords: Stilbenes, o-substituted; Deuteriated compounds