Synthesis of 1,2-aminoalcohols by Ti(IV)-catalyzed photohydroxymethylation of chiral aldimines
摘要:
The N-(alpha-phenylethyl) alkylated aldimines 3a-c are conveniently hydroxymethylated with moderate diastereoselectivities by means of irradiation in methanolic solution in the presence of titanium(IV)chloride. (C) 1998 Elsevier Science Ltd. All rights reserved.
Synthesis of 1,2-aminoalcohols by Ti(IV)-catalyzed photohydroxymethylation of chiral aldimines
摘要:
The N-(alpha-phenylethyl) alkylated aldimines 3a-c are conveniently hydroxymethylated with moderate diastereoselectivities by means of irradiation in methanolic solution in the presence of titanium(IV)chloride. (C) 1998 Elsevier Science Ltd. All rights reserved.
Synthesis of 1,2-aminoalcohols by Ti(IV)-catalyzed photohydroxymethylation of chiral aldimines
作者:Axel G Griesbeck、Stefan Buhr、Johann Lex
DOI:10.1016/s0040-4039(98)00339-6
日期:1998.4
The N-(alpha-phenylethyl) alkylated aldimines 3a-c are conveniently hydroxymethylated with moderate diastereoselectivities by means of irradiation in methanolic solution in the presence of titanium(IV)chloride. (C) 1998 Elsevier Science Ltd. All rights reserved.