Zinc diiodide-promoted synthesis of trisubstituted allenes from propargylic amines
Author:
Affiliation:
1. State Key Laboratory of Organometallic Chemistry
2. Shanghai Institute of Organic Chemistry
3. Chinese Academy of Sciences
4. Shanghai 200032
5. P. R. China
Abstract
Zinc diiodide has been identified as an effective reagent for the efficient synthesis of trisubstituted allenes from propargylic amines.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/QO/C5QO00047E
Reference57 articles.
1. Cascade Radical Cyclizations via Biradicals Generated from Enediynes, Enyne-Allenes, and Enyne-Ketenes
2. Synthesis and Reactions of Allylic, Allenic, Vinylic, and Arylmetal Reagents from Halides and Esters via Transient Organopalladium Intermediates
3. New and Selective Transition Metal Catalyzed Reactions of Allenes
4. Palladium-Catalyzed Reactions of Allenes
5. Reactions of Electron-Deficient Alkynes and Allenes under Phosphine Catalysis
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