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Updated: Jul 5, 2026

Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
06:46

Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate

Published on: June 21, 2017

1,3-ダイオール合成は,制御された,激素媒介C-H機能化によるものです.

Ke Chen1, Jeremy M Richter, Phil S Baran

  • 1Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.

Journal of the American Chemical Society
|May 17, 2008
PubMed
まとめ

新しい方法では,ラジカル媒介C-H機能化を用いてアルコールから1,3-ジオールを合成する. この効率的でスケーラブルなプロセスは,価値ある化学化合物を合成するための実用的な代替案を提供します.

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Diels–Alder Reaction Forming Cyclic Products: Stereochemistry

The Diels–Alder reaction is one of the robust methods for synthesizing unsaturated six-membered rings. The reaction involves a concerted cyclic movement of six π electrons: four π electrons from the diene and two π electrons from the dienophile.
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[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

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