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Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres

Chemical communications (Cambridge, England), 2014-01, Vol.50 (84), p.12597-12611

2014

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Developing Comprehensive Computational Parameter Sets To Describe the Performance of Pyridine-Oxazoline and Related Ligands

ACS catalysis, 2017-06, Vol.7 (6), p.4144-4151

2017

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Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres

Chemical science (Cambridge), 2017-01, Vol.8 (1), p.627-630

2017

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Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides

Beilstein journal of organic chemistry, 2013-03, Vol.9 (1), p.526-532

2013

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Oxenoids in organic synthesis

Organic & biomolecular chemistry, 2014-03, Vol.12 (1), p.1535-1546

2014

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

Nature (London), 2012-10, Vol.490 (7421), p.522-526

2012

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All-Carbon Quaternary Stereogenic Centers in Acyclic Systems through the Creation of Several C–C Bonds per Chemical Step

Journal of the American Chemical Society, 2014-02, Vol.136 (7), p.2682-2694

2014

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Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentresDedicated to my dear friend and colleague Prof. Zeev Gross on the occasion of his 60th birthday

2014-09

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Stereodefined trisubstituted enolates as a unique entry to all-carbon quaternary stereogenic centers in acyclic systems

Nature protocols, 2013-04, Vol.8 (4), p.749-754

2013

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Flexible interactions of the rare-earth elements Y, La, and Lu with phosphorus in metallacyclohexane rings

Chemical science (Cambridge), 2024-07, Vol.15 (30), p.12138-12147

2024

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Engineering Catalysts for Selective Ester Hydrogenation

Organic process research & development, 2020-03, Vol.24 (3), p.415-442

2020

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Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentresElectronic supplementary information (ESI) available. CCDC 1488151. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc03036j

2016-12

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Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres† †Electronic supplementary information (ESI) available. CCDC 1488151. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc03036j Click here for additional data file. Click here for additional data file

Chemical science (Cambridge), 2016-09, Vol.8 (1), p.627-630

2016

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ChemInform Abstract: Stereodefined Acyclic Trisubstituted Metal Enolates Towards the Asymmetric Formation of Quaternary Carbon Stereocenters

ChemInform, 2014-12, Vol.45 (51), p.no-no

2014

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ChemInform Abstract: Oxenoids in Organic Synthesis

ChemInform, 2014-04, Vol.45 (15), p.no-no

2014

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Advances in Carbolithiation

Lithium Compounds in Organic Synthesis, 2014, p.329-350

2014

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Carbometallation Reactions

Metal‐Catalyzed Cross‐Coupling Reactions and More, 2014, p.763-874

2014

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ChemInform Abstract: All-Carbon Quaternary Stereogenic Centers in Acyclic Systems Through the Creation of Several C-C Bonds per Chemical Step

ChemInform, 2014-06, Vol.45 (23), p.no-no

2014

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Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres

Developing Comprehensive Computational Parameter Sets To Describe the Performance of Pyridine-Oxazoline and Related Ligands

Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres

Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides

Oxenoids in organic synthesis

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

All-Carbon Quaternary Stereogenic Centers in Acyclic Systems through the Creation of Several C–C Bonds per Chemical Step

Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentresDedicated to my dear friend and colleague Prof. Zeev Gross on the occasion of his 60th birthday

Stereodefined trisubstituted enolates as a unique entry to all-carbon quaternary stereogenic centers in acyclic systems

Flexible interactions of the rare-earth elements Y, La, and Lu with phosphorus in metallacyclohexane rings

Engineering Catalysts for Selective Ester Hydrogenation

ChemInform Abstract: Stereodefined Acyclic Trisubstituted Metal Enolates Towards the Asymmetric Formation of Quaternary Carbon Stereocenters

ChemInform Abstract: Oxenoids in Organic Synthesis

Advances in Carbolithiation

Carbometallation Reactions

ChemInform Abstract: All-Carbon Quaternary Stereogenic Centers in Acyclic Systems Through the Creation of Several C-C Bonds per Chemical Step

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