The efficient stereoselective synthesis of Z-vinylsilanes through the Suzuki-Miyaura coupling of Z-(α-silylvinyl)borinates-Reference-Cited by-同舟云学术

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The efficient stereoselective synthesis of Z-vinylsilanes through the Suzuki-Miyaura coupling of Z-(α-silylvinyl)borinates

Published:1998-06 Issue:23 Volume:39 Page:3989-3990
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Soderquist John A.,León Gisela

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

2. Asymmetric dihydroxylation of vinyl and allylsilanes

3. Synthetic methods

4. A CONVENIENT STEREOSPECIFIC SYNTHESIS OF α,β-UNSATURATED CARBOXYLIC ESTERS VIA THE PALLADIUM-CATALYZED CARBONYLATION OF 1-ALKENYLBORANES

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1. B-Alkyl sp3–sp2 Suzuki–Miyaura Couplings under Mild Aqueous Micellar Conditions;Organic Letters;2018-05-08

2. Tetrakis(triphenylphosphine)palladium(0);Fieser and Fieser's Reagents for Organic Synthesis;2017-02-21

3. Tetrakis(triphenylphosphine)palladium(0);Fieser and Fieser's Reagents for Organic Synthesis;2017-02-21

4. Synthesis of 4-silaspiro[3.4]octa-1,5-diene derivatives: hybrid spiro compounds;Applied Organometallic Chemistry;2015-03-23

5. Organoboron Chemistry;Organometallics in Synthesis: A Manual;2013-06-26

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