Novel diastereoselective allene formation by an ene reaction of significantly twisted 1,3-dienes with singlet oxygen
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Hydroxy-directed regio-diastereoselective ene reaction of singlet oxygen with chiral allylic alcohols
2. Diastereoselective Singlet Oxygen Ene Reaction (Schenck Reaction) and Diastereoselective Epoxidations of Heteroatom-Substituted Acyclic Chiral Olefins: A Mechanistic Comparison
3. Abnormally high reactivity of the vinyl hydrogen toward singlet oxygen in twisted 1,3-diene
4. Further demonstration of the higher reactivity of the vinyl hydrogen rather than the allyl hydrogen towards singlet oxygen
5. Photosensitized Oxygenation of Twisted 1,3-Dienes: Abnormally Higher Reactivity of Vinyl Hydrogen Rather than Allyl Hydrogen toward Singlet Oxygen
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Stereoselective Photooxidations by the Schenck Ene Reaction;ChemPhotoChem;2018-05-29
2. ChemInform Abstract: Novel Diastereoselective Allene Formation by an Ene Reaction of Significantly Twisted 1,3-Dienes with Singlet Oxygen.;ChemInform;2010-06-12
3. Highly Activated Vinyl Hydrogen in a Significantly Twisted Styrene;The Journal of Organic Chemistry;2006-10-27
4. Stereocontrolled Total Synthesis of a Polyfunctional Carotenoid, Peridinin;The Journal of Organic Chemistry;2004-10-21
5. Ene-Reactions with Singlet Oxygen;CRC Handbookof Organic Photochemistry and Photobiology, Volumes 1 & 2, Second Edition;2003-09-29
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