Electroreductive coupling of aromatic ketones, aldehydes, and aldimines with α,β-unsaturated esters: Synthesis of 5-aryl substituted γ-butyrolactones and lactams-Reference-Cited by-同舟云学术

Electroreductive coupling of aromatic ketones, aldehydes, and aldimines with α,β-unsaturated esters: Synthesis of 5-aryl substituted γ-butyrolactones and lactams

Published:2017-02 Issue:8 Volume:73 Page:1143-1156
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kise Naoki,Hamada Yusuke,Sakurai Toshihiko

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference36 articles.

1. Electroreductive hydrocoupling of activated olefins with ketones or aldehydes in the presence of trimethylchlorosilane

2. NEW ZINC PROMOTED SYNTHETIC REACTION OF γ-BUTYROLACTONE DERIVATIVES

3. Conversion of ketones having δ, ϵ-π-functions to cyclopentanols by zinc-trimethylchlorosilane

4. SmI2-induced reductive cross-coupling of carbonyl compounds with (α,β-unsaturated esters

5. Reductive coupling of ketones or aldehydes with electron-deficient alkenes promoted by samarium di-iodide

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