Literature DB >> 27940818

The broadening reach of frustrated Lewis pair chemistry.

Douglas W Stephan1.   

Abstract

The revelation that combinations of Lewis acids and bases for which dative bonding is impeded can activate dihydrogen led to the concept of "frustrated Lewis pairs" (FLPs). Over the past decade, a range of FLP systems and substrate molecules have precipitated a paradigm change in main-group chemistry and metal-free catalysis. The FLP motif has also found application in a growing body of chemical problems in organic synthesis, transition metal and free radical chemistry, materials, enzymatic models, and surface chemistry. The current state of FLP chemistry is assessed herein, and the outlook for the future considered.
Copyright © 2016, American Association for the Advancement of Science.

Entities:  

Year:  2016        PMID: 27940818     DOI: 10.1126/science.aaf7229

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  79 in total

1.  B(C6F5)3-Catalyzed Direct C3 Alkylation of Indoles and Oxindoles.

Authors:  Shyam Basak; Ana Alvarez-Montoya; Laura Winfrey; Rebecca L Melen; Louis C Morrill; Alexander P Pulis
Journal:  ACS Catal       Date:  2020-04-09       Impact factor: 13.084

2.  Halogenated triphenylgallium and -indium in frustrated Lewis pair activations and hydrogenation catalysis.

Authors:  Maotong Xu; Josephine Possart; Alexander E Waked; Julie Roy; Werner Uhl; Douglas W Stephan
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2017-08-28       Impact factor: 4.226

3.  Enantioselective Conia-Ene-Type Cyclizations of Alkynyl Ketones through Cooperative Action of B(C6F5)3, N-Alkylamine and a Zn-Based Catalyst.

Authors:  Min Cao; Ahmet Yesilcimen; Masayuki Wasa
Journal:  J Am Chem Soc       Date:  2019-02-27       Impact factor: 15.419

Review 4.  On the concept of frustrated Lewis pairs.

Authors:  Frédéric-Georges Fontaine; Douglas W Stephan
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2017-08-28       Impact factor: 4.226

5.  Catalytic Deuterium Incorporation within Metabolically Stable β-Amino C-H Bonds of Drug Molecules.

Authors:  Yejin Chang; Ahmet Yesilcimen; Min Cao; Yuyang Zhang; Bochao Zhang; Jessica Z Chan; Masayuki Wasa
Journal:  J Am Chem Soc       Date:  2019-09-09       Impact factor: 15.419

6.  Isolation, characterization and reactivity of three-coordinate phosphorus dications isoelectronic to alanes and silylium cations.

Authors:  Paul Mehlmann; Tim Witteler; Lukas F B Wilm; Fabian Dielmann
Journal:  Nat Chem       Date:  2019-10-21       Impact factor: 24.427

7.  B(C6F5)3-Catalyzed α-Deuteration of Bioactive Carbonyl Compounds with D2O.

Authors:  Yejin Chang; Tanner Myers; Masayuki Wasa
Journal:  Adv Synth Catal       Date:  2019-11-26       Impact factor: 5.837

8.  B(C6F5)3-Catalyzed C-H Alkylation of N-Alkylamines Using Silicon Enolates without External Oxidant.

Authors:  Jessica Z Chan; Yejin Chang; Masayuki Wasa
Journal:  Org Lett       Date:  2019-01-29       Impact factor: 6.005

9.  A silicon-carbonyl complex stable at room temperature.

Authors:  Chelladurai Ganesamoorthy; Juliane Schoening; Christoph Wölper; Lijuan Song; Peter R Schreiner; Stephan Schulz
Journal:  Nat Chem       Date:  2020-04-20       Impact factor: 24.427

10.  Direct Conversion of N-Alkylamines to N-Propargylamines through C-H Activation Promoted by Lewis Acid/Organocopper Catalysis: Application to Late-Stage Functionalization of Bioactive Molecules.

Authors:  Jessica Z Chan; Ahmet Yesilcimen; Min Cao; Yuyang Zhang; Bochao Zhang; Masayuki Wasa
Journal:  J Am Chem Soc       Date:  2020-09-11       Impact factor: 15.419

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