Literature DB >> 30049213

Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates.

Eric J Alexy1, Haiming Zhang2, Brian M Stoltz1.   

Abstract

The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted acyclic enol carbonates providing linear α-quaternary ketones is reported. Investigation into the reaction revealed that the use of an electron-deficient phosphinooxazoline ligand renders the enolate geometry of the starting material inconsequential, with the same enantiomer of product obtained in the same level of selectivity regardless of the starting ratio of enolates. As a result, a general method toward acyclic all-carbon quaternary stereocenters has been developed.

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Year:  2018        PMID: 30049213      PMCID: PMC6103296          DOI: 10.1021/jacs.8b05560

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  38 in total

Review 1.  The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters.

Authors:  Elias J Corey; Angel Guzman-Perez
Journal:  Angew Chem Int Ed Engl       Date:  1998-03-02       Impact factor: 15.336

2.  Chemo- and Enantioselective Pd/B Hybrid Catalysis for the Construction of Acyclic Quaternary Carbons: Migratory Allylation of O-Allyl Esters to α- C-Allyl Carboxylic Acids.

Authors:  Taiki Fujita; Tomohiro Yamamoto; Yuya Morita; Hongyu Chen; Yohei Shimizu; Motomu Kanai
Journal:  J Am Chem Soc       Date:  2018-04-26       Impact factor: 15.419

3.  Pseudoephenamine: a practical chiral auxiliary for asymmetric synthesis.

Authors:  Marvin R Morales; Kevin T Mellem; Andrew G Myers
Journal:  Angew Chem Int Ed Engl       Date:  2012-03-27       Impact factor: 15.336

4.  Enantioselective Rhodium-Catalyzed Allylic Alkylation of Prochiral α,α-Disubstituted Aldehyde Enolates for the Construction of Acyclic Quaternary Stereogenic Centers.

Authors:  Timothy B Wright; P Andrew Evans
Journal:  J Am Chem Soc       Date:  2016-11-18       Impact factor: 15.419

5.  Palladium-catalyzed asymmetric allylic alkylation of 2-acylimidazoles as ester enolate equivalents.

Authors:  Barry M Trost; Konrad Lehr; David J Michaelis; Jiayi Xu; Andreas K Buckl
Journal:  J Am Chem Soc       Date:  2010-07-07       Impact factor: 15.419

6.  Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes.

Authors:  Yury Minko; Morgane Pasco; Lukas Lercher; Mark Botoshansky; Ilan Marek
Journal:  Nature       Date:  2012-10-25       Impact factor: 49.962

7.  Stereocontrolled alkylative construction of quaternary carbon centers.

Authors:  David A Kummer; William J Chain; Marvin R Morales; Olga Quiroga; Andrew G Myers
Journal:  J Am Chem Soc       Date:  2008-09-13       Impact factor: 15.419

8.  Uniting C1-Ammonium Enolates and Transition Metal Electrophiles via Cooperative Catalysis: The Direct Asymmetric α-Allylation of Aryl Acetic Acid Esters.

Authors:  Kevin J Schwarz; Jessica L Amos; J Cullen Klein; Dung T Do; Thomas N Snaddon
Journal:  J Am Chem Soc       Date:  2016-04-18       Impact factor: 15.419

9.  Stereodefined Acyclic Polysubstituted Silyl Ketene Aminals: Asymmetric Formation of Aldol Products with Quaternary Carbon Stereocenters.

Authors:  Zackaria Nairoukh; Ilan Marek
Journal:  Angew Chem Int Ed Engl       Date:  2015-10-08       Impact factor: 15.336

10.  Regio- and enantiospecific rhodium-catalyzed allylic substitution with an acyl anion equivalent.

Authors:  P Andrew Evans; Samuel Oliver
Journal:  Org Lett       Date:  2013-11-01       Impact factor: 6.005

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  10 in total

1.  Further Developments and Applications of Oxazoline-Containing Ligands in Asymmetric Catalysis.

Authors:  Robert Connon; Brendan Roche; Balaji V Rokade; Patrick J Guiry
Journal:  Chem Rev       Date:  2021-05-21       Impact factor: 60.622

2.  Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Acyclic α-N-Pyrrolyl/Indolyl Ketones.

Authors:  Remi Lavernhe; Eric J Alexy; Haiming Zhang; Brian M Stoltz
Journal:  Org Lett       Date:  2020-05-18       Impact factor: 6.005

3.  Palladium-catalyzed α,β-dehydrogenation of acyclic ester equivalents promoted by a novel electron deficient phosphinooxazoline ligand.

Authors:  Tyler J Fulton; Brenda Wu; Eric J Alexy; Haiming Zhang; Brian M Stoltz
Journal:  Tetrahedron       Date:  2019-06-01       Impact factor: 2.457

4.  Catalytic Asymmetric Allylic Amination with Isatins, Sulfonamides, Imides, Amines, and N-Heterocycles.

Authors:  Ciarán C Lynch; Kaluvu Balaraman; Christian Wolf
Journal:  Org Lett       Date:  2020-04-07       Impact factor: 6.005

5.  Catalytic Enantioselective Synthesis of α-Difunctionalized Cyclic Sulfones.

Authors:  Eleanor Bowen; Gillian Laidlaw; Bethany C Atkinson; Timur A McArdle-Ismaguilov; Vilius Franckevičius
Journal:  J Org Chem       Date:  2022-07-08       Impact factor: 4.198

6.  Asymmetric, visible light-mediated radical sulfinyl-Smiles rearrangement to access all-carbon quaternary stereocentres.

Authors:  Cédric Hervieu; Mariia S Kirillova; Tatiana Suárez; Marco Müller; Estíbaliz Merino; Cristina Nevado
Journal:  Nat Chem       Date:  2021-04-08       Impact factor: 24.427

7.  Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of Thietane 1,1-Dioxides.

Authors:  Gillian Laidlaw; Vilius Franckevičius
Journal:  Org Lett       Date:  2021-12-16       Impact factor: 6.005

8.  Asymmetric construction of acyclic quaternary stereocenters via direct enantioselective additions of α-alkynyl ketones to allenamides.

Authors:  Jiawen Wang; Faqian He; Xiaoyu Yang
Journal:  Nat Commun       Date:  2021-11-18       Impact factor: 14.919

9.  Copper(I)-Catalyzed Synthesis of Unsymmetrical All-Carbon Bis-Quaternary Centers at the Opposing α-Carbons of Cyclohexanones.

Authors:  Joshua A Malone; Satish Chandra Philkhana; Jacob R Stepherson; Fatimat O Badmus; Frank R Fronczek; Rendy Kartika
Journal:  Org Lett       Date:  2022-06-29       Impact factor: 6.072

Review 10.  The Allylic Alkylation of Ketone Enolates.

Authors:  Lukas Junk; Uli Kazmaier
Journal:  ChemistryOpen       Date:  2020-09-10       Impact factor: 2.630

  10 in total

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