The Reaction of Alkenylboranes with Palladium Acetate. Stereoselective Synthesis of Olefinic Derivatives
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/53/6/53_6_1670/_pdf
Reference28 articles.
1. Convenient synthesis of trans olefins from alkynes via hydroboration-cyanohalogenation
2. Methylcopper induced coupling of dialkenylchloroboranes. New procedure for the stereoselective synthesis of (E,E)-1,3-dienes
3. Reaction of Bis(trans-1-hexenyl)methylborane with Two Molar Equivalents of Methylcopper(I). Evidence for the Presence oftrans-1-Hexenylcopper(I) as an Intermediate
4. Methylcopper induced coupling of dialkenylchloroboranes. New procedure for the stereoselective synthesis of (E,E)-1,3-dienes
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3. Stereodefined Construction of Trisubstituted Alkenes by Direct Coupling Reaction of Allylating Agents, Alkynes, and Organoboranes;Chemistry - A European Journal;2012-05-30
4. Selectivity in Palladium-Catalyzed Allylic Substitution;Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis;2011
5. Preparation of Olefins;Compendium of Organic Synthetic Methods;2006-11-22
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