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Organocatalytic regiospecific synthesis of 1H-indene-2-carbaldehyde derivatives: suppression of cycloolefin isomerisation by employing sterically demanding catalysts†
Organic & Biomolecular Chemistry ( IF 2.9 ) Pub Date : 2016-11-08 00:00:00 , DOI: 10.1039/c6ob01918h
Hui Mao 1, 2, 3, 4 , Dong Wan Kim 1, 2, 3, 4 , Hun Yi Shin 1, 2, 3, 4 , Choong Eui Song 2, 3, 4, 5 , Jung Woon Yang 1, 2, 3, 4
Affiliation  

The regiospecific synthesis of 1H-indene-2-carbaldehyde derivatives was achieved through transition-metal-free, reductive cyclisation of ortho-formyl trans-cinnamaldehydes with Hantzsch ester in the presence of an aminocatalyst. In particular, cycloolefin isomerisation of the resulting products could be inhibited efficiently by the introduction of a sterically demanding stereo-defined aminocatalyst.

中文翻译:

1 H-茚2-甲醛衍生物的有机催化区域特异性合成:通过使用空间要求苛刻的催化剂来抑制环烯烃异构化

1 H-茚-2-甲醛衍生物的区域特异性合成是通过在氨基催化剂存在下用Hantzsch酯进行无过渡金属还原的甲酰基反式肉桂醛的环化反应而实现的。特别地,通过引入空间上需要的立体确定的氨基催化剂,可以有效地抑制所得产物的环烯烃异构化。
更新日期:2016-11-08
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