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Metal-Catalyzed Asymmetric Hydrogenation of CN Bonds

ACS catalysis, 2021-01, Vol.11 (1), p.215-247

2021

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Asymmetric C(sp2)H Activation

Chemistry : a European journal, 2013-10, Vol.19 (42), p.14010-14017

2013

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Asymmetric, Nearly Barrierless C(sp3)–H Activation Promoted by Easily-Accessible N-Protected Aminosulfoxides as New Chiral Ligands

ACS catalysis, 2019-03, Vol.9 (3), p.2532-2542

2019

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Synthesis of Axially Chiral C–N Scaffolds via Asymmetric Coupling with Enantiopure Sulfinyl Iodanes

ACS catalysis, 2018-04, Vol.8 (4), p.2805-2809

2018

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C-H Activation for Asymmetric Synthesis

1, 2019

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Visible‐Light‐Triggered, Metal‐ and Photocatalyst‐Free Acylation of N‐Heterocycles

Advanced synthesis & catalysis, 2018-11, Vol.360 (21), p.4184-4190

2018

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Synthesis of Axially Chiral Biaryls through Sulfoxide-Directed Asymmetric Mild CH Activation and Dynamic Kinetic Resolution

Angewandte Chemie (International ed.), 2014-12, Vol.53 (50), p.13871-13875

2014

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Stereoselective Sulfinyl Aniline‐Promoted Pd‐Catalyzed C−H Arylation and Acetoxylation of Aliphatic Amides

Chemistry : a European journal, 2017-11, Vol.23 (62), p.15594-15600

2017

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Highly Efficient One-Pot Access to Functionalized Arylboronic Acids via Noncryogenic Bromine/Magnesium Exchanges

Organic letters, 2011-09, Vol.13 (17), p.4479-4481

2011

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Access to 12-Membered Cyclic ortho,meta-Diarylheptanoids: Total Synthesis of Actinidione via Isomyricanone

Journal of organic chemistry, 2021-02, Vol.86 (3), p.3033-3040

2021

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Stereoselective Metal-Catalyzed C–C Bond Coupling Reactions by Stereoconvergence, Dynamic Kinetic Asymmetric Transformation, or Dynamic Kinetic Resolution

Synthesis (Stuttgart), 2016-09, Vol.48 (18), p.2981-2996

2016

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Enantiopure Sulfinyl Aniline as a Removable and Recyclable Chiral Auxiliary for Asymmetric C(sp3)−H Bond Activation

Chemistry : a European journal, 2016-11, Vol.22 (48), p.17397-17406

2016

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Palladium-Catalyzed Intramolecular Direct Arylation of 2‑Bromo-diaryl Sulfoxides via C–H Bond Activation

Organic letters, 2013-05, Vol.15 (10), p.2490-2493

2013

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Transition-Metal-Free Atropo-Selective Synthesis of Biaryl Compounds Based on Arynes

Chemistry : a European journal, 2012-11, Vol.18 (45), p.14232-14236

2012

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P‐Stereogenic Phosphonates via Dynamic Kinetic Resolution: A Route towards Enantiopure Tertiary Phosphine Oxides

European journal of organic chemistry, 2019-12, Vol.2019 (48), p.7836-7841

2019

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Stereoselective Synthesis of P-Chirogenic Dibenzophosphole–Boranes via Aryne Intermediates

Journal of organic chemistry, 2012-07, Vol.77 (14), p.6117-6127

2012

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Stereoselective Synthesis of o-Bromo (or Iodo)aryl P-Chirogenic Phosphines Based on Aryne Chemistry

Journal of organic chemistry, 2012-07, Vol.77 (13), p.5759-5769

2012

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Iron-catalyzed cross-coupling between C-bromo mannopyranoside derivatives and a vinyl Grignard reagent: toward the synthesis of the C31–C52 fragment of amphidinol 3

Tetrahedron, 2013-09, Vol.69 (36), p.7759-7770

2013

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Increased Potency and Selectivity for Group III Metabotropic Glutamate Receptor Agonists Binding at Dual sites

Journal of medicinal chemistry, 2018-03, Vol.61 (5), p.1969-1989

2018

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Mild deprotection of PMB ethers using tert-butyl bromide

Tetrahedron letters, 2015-12, Vol.56 (49), p.6823-6826

2015

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Efficient and Complementary Methods Offering Access to Synthetically Valuable 1,2-Dibromobenzenes

European Journal of Organic Chemistry, 2011-01, Vol.2011 (2), p.327-340

2011

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Axial Chirality Control During Suzuki−Miyaura Cross-Coupling Reactions: The tert-Butylsulfinyl Group as an Efficient Chiral Auxiliary

Organic letters, 2009-11, Vol.11 (22), p.5130-5133

2009

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Isolation, structural determination and synthetic approaches toward amphidinol 3

Natural product reports, 2014-01, Vol.31 (4), p.468-488

2014

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Diastereoselective synthesis of the C14–C29 fragment of amphidinol 3

Organic & biomolecular chemistry, 2013-10, Vol.11 (39), p.6829

2013

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Diastereoselective synthesis of the C17-C30 fragment of amphidinol 3

Organic & biomolecular chemistry, 2012-12, Vol.10 (47), p.9418-9428

2012

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Metal-Catalyzed Asymmetric Hydrogenation of CN Bonds

Asymmetric C(sp2)H Activation

Asymmetric, Nearly Barrierless C(sp3)–H Activation Promoted by Easily-Accessible N-Protected Aminosulfoxides as New Chiral Ligands

Synthesis of Axially Chiral C–N Scaffolds via Asymmetric Coupling with Enantiopure Sulfinyl Iodanes

C-H Activation for Asymmetric Synthesis

Visible‐Light‐Triggered, Metal‐ and Photocatalyst‐Free Acylation of N‐Heterocycles

Synthesis of Axially Chiral Biaryls through Sulfoxide-Directed Asymmetric Mild CH Activation and Dynamic Kinetic Resolution

Stereoselective Sulfinyl Aniline‐Promoted Pd‐Catalyzed C−H Arylation and Acetoxylation of Aliphatic Amides

Highly Efficient One-Pot Access to Functionalized Arylboronic Acids via Noncryogenic Bromine/Magnesium Exchanges

Access to 12-Membered Cyclic ortho,meta-Diarylheptanoids: Total Synthesis of Actinidione via Isomyricanone

Stereoselective Metal-Catalyzed C–C Bond Coupling Reactions by Stereoconvergence, Dynamic Kinetic Asymmetric Transformation, or Dynamic Kinetic Resolution

Enantiopure Sulfinyl Aniline as a Removable and Recyclable Chiral Auxiliary for Asymmetric C(sp3)−H Bond Activation

Palladium-Catalyzed Intramolecular Direct Arylation of 2‑Bromo-diaryl Sulfoxides via C–H Bond Activation

Transition-Metal-Free Atropo-Selective Synthesis of Biaryl Compounds Based on Arynes

P‐Stereogenic Phosphonates via Dynamic Kinetic Resolution: A Route towards Enantiopure Tertiary Phosphine Oxides

Stereoselective Synthesis of P-Chirogenic Dibenzophosphole–Boranes via Aryne Intermediates

Stereoselective Synthesis of o-Bromo (or Iodo)aryl P-Chirogenic Phosphines Based on Aryne Chemistry

Iron-catalyzed cross-coupling between C-bromo mannopyranoside derivatives and a vinyl Grignard reagent: toward the synthesis of the C31–C52 fragment of amphidinol 3

Increased Potency and Selectivity for Group III Metabotropic Glutamate Receptor Agonists Binding at Dual sites

Mild deprotection of PMB ethers using tert-butyl bromide

Efficient and Complementary Methods Offering Access to Synthetically Valuable 1,2-Dibromobenzenes

Axial Chirality Control During Suzuki−Miyaura Cross-Coupling Reactions: The tert-Butylsulfinyl Group as an Efficient Chiral Auxiliary

Isolation, structural determination and synthetic approaches toward amphidinol 3

Diastereoselective synthesis of the C14–C29 fragment of amphidinol 3

Diastereoselective synthesis of the C17-C30 fragment of amphidinol 3

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