Vinyl hydrogen more reactive than benzyl hydrogen toward base in significantly twisted styrenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Abnormally high reactivity of the vinyl hydrogen toward singlet oxygen in twisted 1,3-diene
2. Further demonstration of the higher reactivity of the vinyl hydrogen rather than the allyl hydrogen towards singlet oxygen
3. Photosensitized Oxygenation of Twisted 1,3-Dienes: Abnormally Higher Reactivity of Vinyl Hydrogen Rather than Allyl Hydrogen toward Singlet Oxygen
4. Novel diastereoselective allene formation by an ene reaction of significantly twisted 1,3-dienes with singlet oxygen
5. Iodide acceleration in the Pd-catalyzed coupling of aromatic 1,2-ditriflates with alkynes: Synthesis of enediynes
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1. Mixed AggregAte (MAA): A Single Concept for All Dipolar Organometallic Aggregates. 2. Syntheses and Reactivities of Homo/HeteroMAAs;Chemical Reviews;2013-08-16
2. Highly Activated Vinyl Hydrogen in a Significantly Twisted Styrene;The Journal of Organic Chemistry;2006-10-27
3. Vinylic Deprotonation in the Coordination Sphere of Platinum( II ): Regioselective Formation of Alkenyl Complexes;European Journal of Inorganic Chemistry;2004-12
4. Functionalized Organolithium Compounds: New Synthetic Adventures;Current Organic Chemistry;2003-06-01
5. Unique Reactivity of Twisted 1,3-Diene;Journal of Synthetic Organic Chemistry, Japan;2003
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