Literature DB >> 21755089

Silicon-based cross-coupling reaction: an environmentally benign version.

Yoshiaki Nakao1, Tamejiro Hiyama.   

Abstract

Much attention has been paid to the cross-coupling reaction of organosilicon compounds due to their stability, non-toxicity, and natural abundance of silicon. In addition, the silicon-based cross-coupling has many advantages over other cross-coupling protocols. Successful examples of the silicon-based cross-coupling reaction are reviewed, focusing especially on the advances made in the last decade. Having had a number of highly effective palladium catalysts developed mainly for other cross-coupling reactions, the development of the silicon-based protocol owes heavily to the design of organosilicon reagents which effectively undergo transmetalation, a key elemental step of the silicon-based cross-coupling reaction. This tutorial review thus classifies various organosilicon reagents depending on substituents on silicon and surveys their cross-coupling reactions with various electrophiles. This journal is © The Royal Society of Chemistry 2011

Entities:  

Year:  2011        PMID: 21755089     DOI: 10.1039/c1cs15122c

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  59 in total

1.  Umpolung α-Silylation of Cyclopropyl Acetates via Low-Temperature Catalytic C-C Activation.

Authors:  Thirupataiah Avullala; Parham Asgari; Yuanda Hua; Apparao Bokka; Shawn G Ridlen; Kyungsuk Yum; H V Rasika Dias; Junha Jeon
Journal:  ACS Catal       Date:  2018-12-03       Impact factor: 13.084

2.  Palladium-Catalyzed Transformations of Alkyl C-H Bonds.

Authors:  Jian He; Masayuki Wasa; Kelvin S L Chan; Qian Shao; Jin-Quan Yu
Journal:  Chem Rev       Date:  2016-12-02       Impact factor: 60.622

3.  Preparation of allyl and vinyl silanes by the palladium-catalyzed silylation of terminal olefins: a silyl-Heck reaction.

Authors:  Jesse R McAtee; Sara E S Martin; Derek T Ahneman; Keywan A Johnson; Donald A Watson
Journal:  Angew Chem Int Ed Engl       Date:  2012-03-01       Impact factor: 15.336

4.  Ligand-enabled cross-coupling of C(sp(3))-H bonds with arylsilanes.

Authors:  Jian He; Ryosuke Takise; Haiyan Fu; Jin-Quan Yu
Journal:  J Am Chem Soc       Date:  2015-04-02       Impact factor: 15.419

5.  Iridium-Catalyzed Silylation of C-H Bonds in Unactivated Arenes: A Sterically Encumbered Phenanthroline Ligand Accelerates Catalysis.

Authors:  Caleb Karmel; Zhewei Chen; John F Hartwig
Journal:  J Am Chem Soc       Date:  2019-04-23       Impact factor: 15.419

6.  Simplified Preparation of Trialkylvinylsilanes via the Silyl-Heck Reaction Utilizing a Second Generation Catalyst.

Authors:  Jesse R McAtee; Sarah B Krause; Donald A Watson
Journal:  Adv Synth Catal       Date:  2015-07-14       Impact factor: 5.837

7.  Enantioselective Synthesis of Nonracemic Geminal Silylboronates by Pt-Catalyzed Hydrosilylation.

Authors:  Adam A Szymaniak; Chenlong Zhang; John R Coombs; James P Morken
Journal:  ACS Catal       Date:  2018-02-23       Impact factor: 13.084

8.  Iridium-Catalyzed Silylation of Five-Membered Heteroarenes: High Sterically Derived Selectivity from a Pyridyl-Imidazoline Ligand.

Authors:  Caleb Karmel; Camille Z Rubel; Elena V Kharitonova; John F Hartwig
Journal:  Angew Chem Weinheim Bergstr Ger       Date:  2020-01-22

9.  Silver catalyzed proto- and sila-Nakamura-type α-vinylation of silyl enol ethers with dichloroacetylene. Divergent formation of stereochemically pure tri- and tetrasubstituted olefins.

Authors:  Lun Li; Kimberly A Wasik; Brian J Frost; Laina M Geary
Journal:  Tetrahedron Lett       Date:  2019-11-06       Impact factor: 2.415

10.  Understanding Site Selectivity in the Palladium-Catalyzed Cross-Coupling of Allenylsilanolates.

Authors:  Scott E Denmark; Andrea Ambrosi
Journal:  Synlett       Date:  2017-07-12       Impact factor: 2.454

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.