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引用本文的文献

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Stereoselective electrochemical intramolecular imino-pinacol reaction: a straightforward entry to enantiopure piperazines.立体选择性电化学分子内亚氨基频哪醇反应：对映体纯哌嗪的直接合成方法
Beilstein J Org Chem. 2025 Sep 12;21:1897-1908. doi: 10.3762/bjoc.21.147. eCollection 2025.

Diastereoselective reductive imino-aldol reaction of alpha-imino esters promoted by titanium tetraiodide: synthesis of alpha,beta-diamino esters.

作者信息

Shimizu Makoto, Inayoshi Koji, Sahara Tetsuya

机构信息

Department of Chemistry for Materials, Mie University, Tsu, Mie 514-8507, Japan.

出版信息

Org Biomol Chem. 2005 Jun 21;3(12):2237-8. doi: 10.1039/b505335h. Epub 2005 May 18.

DOI:10.1039/b505335h
PMID:16010355
Abstract

Under the influence of titanium tetraiodide reductive imino-aldol reaction of the N-tosylimine derived from ethyl glyoxylate proceeded with aldimines to give alpha,beta-diamino esters in good yields in a highly diastereoselective manner.

摘要