Literature DB >> 21677934

The asymmetric Heck and related reactions.

Dennis Mc Cartney1, Patrick J Guiry.   

Abstract

The asymmetric inter- and intramolecular Heck and related reactions are comprehensively reviewed, from their original development to recent advances in terms of substrate scope, reactivity, regio- and enantioselectivity. Their reaction mechanisms/catalytic cycles are discussed in order to understand the concepts underpinning the significant recent developments of these processes. The design and application of new chiral ligands has been pivotal to reaction enhancements and, for each Heck and related process, we classify ligands by the nature of the denticity, chirality and donor atoms involved. In this manner, the continued development of ligand architectural design and application can be more easily monitored for each process. Significant improvements in reaction times, a disadvantage in many Heck reactions, have been addressed through a combination the use of microwave-assisted protocols and ligand design. The asymmetric Fujiwara-Moritani and oxidative boron Heck-type reactions, recent additions to Heck type processes, will also be discussed in this critical review (149 references). This journal is © The Royal Society of Chemistry 2011

Entities:  

Year:  2011        PMID: 21677934     DOI: 10.1039/c1cs15101k

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


  42 in total

Review 1.  Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C Bonds.

Authors:  Alan H Cherney; Nathaniel T Kadunce; Sarah E Reisman
Journal:  Chem Rev       Date:  2015-08-13       Impact factor: 60.622

2.  Practical Intermolecular Hydroarylation of Terminal Alkenes via Reductive Heck Coupling.

Authors:  John A Gurak; Keary M Engle
Journal:  ACS Catal       Date:  2018-08-24       Impact factor: 13.084

3.  Alkenyl carbonyl derivatives in enantioselective redox relay Heck reactions: accessing α,β-unsaturated systems.

Authors:  Chun Zhang; Celine B Santiago; Lei Kou; Matthew S Sigman
Journal:  J Am Chem Soc       Date:  2015-06-04       Impact factor: 15.419

4.  Relative reactivity of alkenyl alcohols in the palladium-catalyzed redox-relay Heck reaction.

Authors:  Margaret J Hilton; Bin Cheng; Benjamin R Buckley; Liping Xu; Olaf Wiest; Matthew S Sigman
Journal:  Tetrahedron       Date:  2015-09-16       Impact factor: 2.457

5.  Enantioselective Heck arylations of acyclic alkenyl alcohols using a redox-relay strategy.

Authors:  Erik W Werner; Tian-Sheng Mei; Alexander J Burckle; Matthew S Sigman
Journal:  Science       Date:  2012-12-14       Impact factor: 47.728

6.  Enantioselective Dehydrogenative Heck Arylations of Trisubstituted Alkenes with Indoles to Construct Quaternary Stereocenters.

Authors:  Chun Zhang; Celine B Santiago; Jennifer M Crawford; Matthew S Sigman
Journal:  J Am Chem Soc       Date:  2015-12-10       Impact factor: 15.419

7.  Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.

Authors:  Elizabeth C Swift; Elizabeth R Jarvo
Journal:  Tetrahedron       Date:  2013-07-22       Impact factor: 2.457

8.  Catalyst-controlled regioselectivity in the synthesis of branched conjugated dienes via aerobic oxidative Heck reactions.

Authors:  Changwu Zheng; Dian Wang; Shannon S Stahl
Journal:  J Am Chem Soc       Date:  2012-09-28       Impact factor: 15.419

9.  Nickel-Catalyzed Dicarbofunctionalization of Alkenes.

Authors:  Xiaoxu Qi; Tianning Diao
Journal:  ACS Catal       Date:  2020-07-02       Impact factor: 13.084

10.  Enantioselective redox-relay oxidative heck arylations of acyclic alkenyl alcohols using boronic acids.

Authors:  Tian-Sheng Mei; Erik W Werner; Alexander J Burckle; Matthew S Sigman
Journal:  J Am Chem Soc       Date:  2013-04-24       Impact factor: 15.419

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