2-Allylisourea as a Starting Material for Palladium-Catalyzed Wittig-Type Allylidenation of Aldehydes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/59/4/59_4_1279/_pdf
Reference8 articles.
1. Organopalladium intermediates in organic synthesis
2. Metal Complexes in Organic Synthesis. VIII. Allylic Alcohols as Starting Materials in Palladium-catalyzed Wittig-type Olefinizations
3. A Convenient Method for the Preparation of Conjugated Olefins from Allylic Acetates and Aldehydes. Synthesis of Pellitorine
4. N-Allylation of Imides Catalyzed by Palladium(0)
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1. Isoureas: Versatile Alkylation Reagents in Organic Chemistry;Synlett;2009-05-07
2. Palladium(0)-catalyzed direct cross-coupling reaction of allylic alcohols with aryl- and alkenylboronic acids;Organic & Biomolecular Chemistry;2008
3. Stereoselective Synthesis of (E)- and (Z)-Allylphosphonium Salts by Palladium-Catalyzed Addition of Phosphine to Allene;Advanced Synthesis & Catalysis;2001-01-29
4. Stereochemistry of Carbenic 1,2-Vinyl Shifts;The Journal of Organic Chemistry;1998-01-23
5. An expeditious preparation of .eta.3-allylpalladium tetrafluoroborates using the 2,4,6-triphenylpyridine neutral leaving group;Organometallics;1994-01
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