The regio- and stereochemical course of reductive cross-coupling reactions between 1,3-disubstituted allenes and vinylsilanes: synthesis of (Z)-dienes-Reference-Cited by-同舟云学术

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The regio- and stereochemical course of reductive cross-coupling reactions between 1,3-disubstituted allenes and vinylsilanes: synthesis of (Z)-dienes

Published:2010-06 Issue:26 Volume:66 Page:4775-4783
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Barlan Allan U.,Micalizio Glenn C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference108 articles.

1. For recent reviews, see:

2. Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes

3. Nickel-catalyzed coupling reactions of alkenes

4. Regioselectivity and enantioselectivity in nickel-catalysed reductive coupling reactions of alkynes

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1. Deciphering the Chameleonic Chemistry of Allenols: Breaking the Taboo of a Onetime Esoteric Functionality;Chemical Reviews;2021-02-25

2. Cooperative Iodide Pd(0)-Catalysed Coupling of Alkoxyallenes and N -Tosylhydrazones: A Selective Synthesis of Conjugated and Skipped Dienes;Chemistry - A European Journal;2018-03-23

3. Reaction Design, Discovery, and Development as a Foundation to Function-Oriented Synthesis;Accounts of Chemical Research;2015-02-10

4. An Annulation Reaction for the Synthesis of Cross-Conjugated Triene-Containing Hydroindanes from Acyclic Precursors;Organic Letters;2014-09-12

5. Carbometallation Reactions;Metal-Catalyzed Cross-Coupling Reactions and More;2013-11-30

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