Literature DB >> 29573527

Highly Stereoselective Synthesis of 1,3-Dienes through an Aryl to Vinyl 1,4-Palladium Migration/Heck Sequence.

Tian-Jiao Hu1, Meng-Yao Li1, Qian Zhao2, Chen-Guo Feng1,3, Guo-Qiang Lin1.   

Abstract

An efficient aryl to vinyl 1,4-palladium migration/Heck sequence was developed for the stereoselective synthesis of 1,3-dienes. High stereoselectivity was observed not only for 1,3-dienes bearing two similar aryl groups at terminal positions, but also for those with configurations shown to be unfavorable with previous methods.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  C−H functionalization; alkenylation; cross-coupling; metal migration; palladium

Year:  2018        PMID: 29573527     DOI: 10.1002/anie.201801963

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

Review 1.  Modern Synthetic Methods for the Stereoselective Construction of 1,3-Dienes.

Authors:  Raquel G Soengas; Humberto Rodríguez-Solla
Journal:  Molecules       Date:  2021-01-06       Impact factor: 4.411

2.  Suzuki-Miyaura Coupling Enabled by Aryl to Vinyl 1,4-Palladium Migration.

Authors:  Meng-Yao Li; Pengbo Han; Tian-Jiao Hu; Dong Wei; Ge Zhang; Anjun Qin; Chen-Guo Feng; Ben Zhong Tang; Guo-Qiang Lin
Journal:  iScience       Date:  2020-03-07
  2 in total

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