Literature DB >> 33570909

Enantioselective Formation of Quaternary Centers by Allylic Alkylation with First-Row Transition-Metal Catalysts.

Lars Süsse1, Brian M Stoltz1.   

Abstract

Asymmetric allylic alkylation mediated by transition metals provides an efficient strategy to form quaternary stereogenic centers. While this transformation is dominated by the use of second- and third-row transition metals (e.g., Pd, Rh, and Ir), recent developments have revealed the potential of first-row transition metals, which provide not only a less expensive and potentially equally efficient alternative but also new mechanistic possibilities. This review summarizes examples for the assembly of quaternary stereocenters using prochiral allylic substrates and hard, achiral nucleophiles in the presence of copper complexes and highlights the complementary approaches with soft, prochiral nucleophiles catalyzed by chiral cobalt and nickel complexes.

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Year:  2021        PMID: 33570909      PMCID: PMC8846597          DOI: 10.1021/acs.chemrev.0c01115

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  61 in total

1.  Bidentate NHC-based chiral ligands for efficient Cu-catalyzed enantioselective allylic alkylations: structure and activity of an air-stable chiral Cu complex.

Authors:  Andrew O Larsen; Wenhao Leu; Christina Nieto Oberhuber; John E Campbell; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2004-09-15       Impact factor: 15.419

2.  Creation of quaternary stereocenters in carbonyl allylation reactions.

Authors:  Ilan Marek; Genia Sklute
Journal:  Chem Commun (Camb)       Date:  2006-12-06       Impact factor: 6.222

3.  Regiodivergent 1,4 versus 1,6 asymmetric copper-catalyzed conjugate addition.

Authors:  Hélène Hénon; Marc Mauduit; Alexandre Alexakis
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

4.  Controllable, Sequential, and Stereoselective C-H Allylic Alkylation of Alkenes.

Authors:  Ling Qin; Mohammed Sharique; Uttam K Tambar
Journal:  J Am Chem Soc       Date:  2019-10-15       Impact factor: 15.419

5.  Construction of Vicinal Quaternary Carbon Centers via Cobalt-Catalyzed Asymmetric Reverse Prenylation.

Authors:  Minghe Sun; Jia-Feng Chen; Shufeng Chen; Changkun Li
Journal:  Org Lett       Date:  2019-02-15       Impact factor: 6.005

Review 6.  Enantioselective formation of quaternary carbon stereocenters in natural product synthesis: a recent update.

Authors:  Chengxi Li; Sherif Shaban Ragab; Guodu Liu; Wenjun Tang
Journal:  Nat Prod Rep       Date:  2020-02-26       Impact factor: 13.423

7.  Formation of quaternary chiral centers by N-heterocyclic carbene-Cu-catalyzed asymmetric conjugate addition reactions with Grignard reagents on trisubstituted cyclic enones.

Authors:  Stefan Kehrli; David Martin; Diane Rix; Marc Mauduit; Alexandre Alexakis
Journal:  Chemistry       Date:  2010-08-23       Impact factor: 5.236

8.  Diastereodivergent Reverse Prenylation of Indole and Tryptophan Derivatives: Total Synthesis of Amauromine, Novoamauromine, and epi-Amauromine.

Authors:  Jonas M Müller; Christian B W Stark
Journal:  Angew Chem Int Ed Engl       Date:  2016-03-11       Impact factor: 15.336

9.  Pentacoordinated carboxylate π-allyl nickel complexes as key intermediates for the Ni-catalyzed direct amination of allylic alcohols.

Authors:  Yusuke Kita; Hironobu Sakaguchi; Yoichi Hoshimoto; Daisuke Nakauchi; Yasuhito Nakahara; Jean-François Carpentier; Sensuke Ogoshi; Kazushi Mashima
Journal:  Chemistry       Date:  2015-08-26       Impact factor: 5.236

10.  Development of biisoquinoline-based chiral diaminocarbene ligands: enantioselective SN2' allylic alkylation catalyzed by copper-carbene complexes.

Authors:  Hwimin Seo; Dimitri Hirsch-Weil; Khalil A Abboud; Sukwon Hong
Journal:  J Org Chem       Date:  2008-02-12       Impact factor: 4.354

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  8 in total

1.  Synthesis of Highly Congested Tertiary Alcohols via the [3,3] Radical Deconstruction of Breslow Intermediates.

Authors:  Roger Machín Rivera; Nikolas R Burton; Luke D Call; Marshall A Tomat; Vincent N G Lindsay
Journal:  Org Lett       Date:  2022-06-03       Impact factor: 6.072

2.  Identifying the Imperative Role of Metal-Olefin Interactions in Catalytic C-O Reductive Elimination from Nickel(II).

Authors:  Trevor D Lohrey; Alexander Q Cusumano; William A Goddard; Brian M Stoltz
Journal:  ACS Catal       Date:  2021-08-02       Impact factor: 13.700

3.  Enantioselective Hydroalkenylation of Olefins with Enol Sulfonates Enabled by Dual Copper Hydride and Palladium Catalysis.

Authors:  Alexander W Schuppe; James Levi Knippel; Gustavo M Borrajo-Calleja; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2021-03-30       Impact factor: 15.419

4.  Skeletal remodeling of chalcone-based pyridinium salts to access isoindoline polycycles and their bridged derivatives.

Authors:  Lele Wang; Huabin Han; Lijie Gu; Wenjing Zhang; Junwei Zhao; Qilin Wang
Journal:  Chem Sci       Date:  2021-11-09       Impact factor: 9.825

5.  Stereospecific Construction of Quaternary Carbon Stereocenters from Quaternary Carbon Stereocenters.

Authors:  Kaushalendra Patel; Veeranjaneyulu Lanke; Ilan Marek
Journal:  J Am Chem Soc       Date:  2022-04-12       Impact factor: 16.383

6.  Doubly stereoconvergent construction of vicinal all-carbon quaternary and tertiary stereocenters by Cu/Mg-catalyzed propargylic substitution.

Authors:  Xiang Pu; Qiu-Di Dang; Lei Yang; Xia Zhang; Dawen Niu
Journal:  Nat Commun       Date:  2022-05-04       Impact factor: 17.694

Review 7.  Construction of Non-Biaryl Atropisomeric Amide Scaffolds Bearing a C-N Axis via Enantioselective Catalysis.

Authors:  Xiao Xiao; Biao Chen; Yi-Ping Yao; Hai-Jie Zhou; Xu Wang; Neng-Zhong Wang; Fen-Er Chen
Journal:  Molecules       Date:  2022-10-04       Impact factor: 4.927

8.  Enantioselective Synthesis of Acyclic Orthogonally Functionalized Compounds Bearing a Quaternary Stereocenter Using Chiral Ammonium Salt Catalysis.

Authors:  Katharina Röser; Bettina Berger; Michael Widhalm; Mario Waser
Journal:  ChemistryOpen       Date:  2021-08       Impact factor: 2.630

  8 in total

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