Mechanistic Studies on the Heck−Mizoroki Cross-Coupling Reaction of a Hindered Vinylboronate Ester as a Key Approach to Developing a Highly Stereoselective Synthesis of a C1−C7 Z,Z,E-Triene Synthon for Viridenomycin-Reference-Cited by-同舟云学术

Mechanistic Studies on the Heck−Mizoroki Cross-Coupling Reaction of a Hindered Vinylboronate Ester as a Key Approach to Developing a Highly Stereoselective Synthesis of a C1−C7 Z,Z,E-Triene Synthon for Viridenomycin

Published:2007-03-01 Issue:7 Volume:72 Page:2525-2532
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Batsanov Andrei S.¹,Knowles Jonathan P.¹,Whiting Andrew¹

Affiliation:

1. University of Durham, Department of Chemistry, Sciences Laboratories South Road DH1 3LE, Durham, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0626010

Reference69 articles.

1. Synthesis of trans-arylvinylboronates via a palladium catalysed cross-coupling of a vinylboronate ester with aryl halides

2. 4,4,6-Trimethyl-2-vinyl-1,3,2-dioxaborinane: a superior 2-carbon building block for vinylboronate Heck couplings

3. A Convergent Stereoselective Total Synthesis of Racemic Phthoxazolin A

Cited by 50 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Regioselective Synthesis of α-Vinyl Boronates via a Pd-Catalyzed Mizoroki–Heck Reaction;Organic Letters;2024-08-30

2. NHC-Pd(II) full pincer catalyzed Mizoroki-Heck Type Cross-Coupling of Vinyl Chloride and Alkenes: Synthesis of Novel Ferrocenylated Conjugated Dienes;Journal of Organometallic Chemistry;2023-01

3. Synthesis and Stability Studies of a Simplified, Thiazole-Containing Macrocycle of the Anticancer Agent Salarin C;Organic Letters;2022-08-17

4. Synthesis and characterization of novel basketing of C-4-phenylocta-phenylhydrazide-calix[4]resorcinarene-PdNPs;VIII INTERNATIONAL ANNUAL CONFERENCE “INDUSTRIAL TECHNOLOGIES AND ENGINEERING” (ICITE 2021);2022

5. Rapid Access to Azabicyclo[3.3.1]nonanes by a Tandem Diverted Tsuji–Trost Process;Chemistry – A European Journal;2020-10-06