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Oxalyl Boronates Enable Modular Synthesis of Bioactive Imidazoles

Angewandte Chemie International Edition, 2017-05, Vol.56 (22), p.6264-6267

International ed. in English, 2017

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Synthesis of Aminoboronic Acid Derivatives from Amines and Amphoteric Boryl Carbonyl Compounds

Angewandte Chemie (International ed.), 2016-10, Vol.55 (41), p.12659-12663

International ed. in English, 2016

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Fragment-based drug discovery: opportunities for organic synthesis

RSC medicinal chemistry, 2020-12, Vol.12 (3), p.321-329

2020

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Boroalkyl Group Migration Provides a Versatile Entry into α-Aminoboronic Acid Derivatives

Journal of the American Chemical Society, 2012-06, Vol.134 (24), p.9926-9929

2012

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Boron-Containing Enamine and Enamide Linchpins in the Synthesis of Nitrogen Heterocycles

Journal of the American Chemical Society, 2014-12, Vol.136 (50), p.17669-17673

2014

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Oxidative Geminal Functionalization of Organoboron Compounds

Angewandte Chemie (International ed.), 2012-10, Vol.51 (44), p.11092-11096

International ed. in English, 2012

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Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates

Organic letters, 2015-12, Vol.17 (23), p.5764-5767

2015

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Amphoteric α‑Boryl Aldehyde Linchpins in the Synthesis of Heterocycles

ACS catalysis, 2015-09, Vol.5 (9), p.5373-5379

2015

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X‑ray Screening of an Electrophilic Fragment Library and Application toward the Development of a Novel ERK 1/2 Covalent Inhibitor

Journal of medicinal chemistry, 2022-09, Vol.65 (18), p.12319-12333

2022

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Development of the Direct Suzuki–Miyaura Cross-Coupling of Primary B‑Alkyl MIDA-boronates and Aryl Bromides

Organic letters, 2014-03, Vol.16 (5), p.1338-1341

2014

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Stereocontrolled Synthesis of 1,2- and 1,3-Diamine Building Blocks from Aziridine Aldehyde Dimers

Journal of organic chemistry, 2013-12, Vol.78 (23), p.11637-11645

2013

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Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach

Organic letters, 2015-11, Vol.17 (22), p.5594-5597

2015

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Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein–Protein Interaction

Journal of medicinal chemistry, 2021-04, Vol.64 (7), p.4071-4088

2021

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Facile synthesis of borofragments and their evaluation in activity-based protein profiling

Chemical communications (Cambridge, England), 2015-02, Vol.51 (17), p.3608-3611

2015

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Stereocontrolled Disruption of the Ugi Reaction toward the Production of Chiral Piperazinones: Substrate Scope and Process Development

Journal of organic chemistry, 2014-11, Vol.79 (21), p.9948-9957

2014

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Activation of Alkynylzinc Reagents by a Hemiaminal‐Driven Catalytic Microenvironment

European journal of organic chemistry, 2017-01, Vol.2017 (2), p.419-423

2017

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Chemoselective palladium-catalyzed α-allylation of α-boryl aldehydes

Organic & biomolecular chemistry, 2012-10, Vol.10 (39), p.7900-7902

2012

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Direct Intramolecular Catalytic Enantioselective Alkylation of Oxazolidinone Bromoalkanoate Imides

Synlett, 2014-10, Vol.25 (19), p.2802-2805

2014

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Novel Synthesis of the Isoflavone Genistein

Synthesis (Stuttgart), 2010-05, Vol.2010 (10), p.1590-1592

2010

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Synthesis of a Novel Chiral Cubane-Based Schiff Base Ligand and Its Application in Asymmetric Nitro-Aldol (Henry) Reactions

Synthesis (Stuttgart), 2010-01, Vol.2010 (1), p.98-102

2010

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An efficient synthesis of daidzein, dimethyldaidzein, and isoformononetin

Tetrahedron letters, 2010-08, Vol.51 (33), p.4408-4410

2010

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Evaluation of a chiral cubane-based Schiff base ligand in asymmetric catalysis reactions

Beilstein journal of organic chemistry, 2012-10, Vol.8 (1), p.1814-1818

2012

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Fragment-Based Discovery of Allosteric Inhibitors of SH2 Domain-Containing Protein Tyrosine Phosphatase‑2 (SHP2)

Journal of medicinal chemistry, 2024-03, Vol.67 (6), p.4655-4675

2024

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Efficient Preparation of α-Aminoboronic Acid Derivatives via Boroalkyl Group Migration

Synthesis (Stuttgart), 2014-02, Vol.46 (4), p.445-454

2014

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Oxalyl Boronates Enable Modular Synthesis of Bioactive Imidazoles

Synthesis of Aminoboronic Acid Derivatives from Amines and Amphoteric Boryl Carbonyl Compounds

Fragment-based drug discovery: opportunities for organic synthesis

Boroalkyl Group Migration Provides a Versatile Entry into α-Aminoboronic Acid Derivatives

Boron-Containing Enamine and Enamide Linchpins in the Synthesis of Nitrogen Heterocycles

Oxidative Geminal Functionalization of Organoboron Compounds

Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates

Amphoteric α‑Boryl Aldehyde Linchpins in the Synthesis of Heterocycles

X‑ray Screening of an Electrophilic Fragment Library and Application toward the Development of a Novel ERK 1/2 Covalent Inhibitor

Development of the Direct Suzuki–Miyaura Cross-Coupling of Primary B‑Alkyl MIDA-boronates and Aryl Bromides

Stereocontrolled Synthesis of 1,2- and 1,3-Diamine Building Blocks from Aziridine Aldehyde Dimers

Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach

Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein–Protein Interaction

Facile synthesis of borofragments and their evaluation in activity-based protein profiling

Stereocontrolled Disruption of the Ugi Reaction toward the Production of Chiral Piperazinones: Substrate Scope and Process Development

Activation of Alkynylzinc Reagents by a Hemiaminal‐Driven Catalytic Microenvironment

Chemoselective palladium-catalyzed α-allylation of α-boryl aldehydes

Direct Intramolecular Catalytic Enantioselective Alkylation of Oxazolidinone Bromoalkanoate Imides

Novel Synthesis of the Isoflavone Genistein

Synthesis of a Novel Chiral Cubane-Based Schiff Base Ligand and Its Application in Asymmetric Nitro-Aldol (Henry) Reactions

An efficient synthesis of daidzein, dimethyldaidzein, and isoformononetin

Evaluation of a chiral cubane-based Schiff base ligand in asymmetric catalysis reactions

Fragment-Based Discovery of Allosteric Inhibitors of SH2 Domain-Containing Protein Tyrosine Phosphatase‑2 (SHP2)

Fragment-Based Discovery of a Series of Allosteric-Binding Site Modulators of β‑Glucocerebrosidase

Efficient Preparation of α-Aminoboronic Acid Derivatives via Boroalkyl Group Migration

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