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Enantioselective Rhodium(III)-Catalyzed Markovnikov Hydroboration of Unactivated Terminal Alkenes

Journal of the American Chemical Society, 2017-07, Vol.139 (27), p.9148-9151

2017

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Diastereodivergent Synthesis of Trisubstituted Alkenes through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone

Angewandte Chemie (International ed.), 2012-12, Vol.51 (50), p.12444-12448

International ed. in English, 2012

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Deubiquitinase-targeting chimeras for targeted protein stabilization

Nature chemical biology, 2022-04, Vol.18 (4), p.412-421

2022

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Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes

Chemical communications (Cambridge, England), 2012-01, Vol.48 (74), p.9230-9232

2012

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Correction to “Rational Chemical Design of Molecular Glue Degraders”

ACS central science, 2023-08, Vol.9 (8), p.1702-1702

2023

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Property-Based Drug Design Merits a Nobel Prize

Journal of medicinal chemistry, 2024-07, Vol.67 (14), p.11452-11458

2024

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Targeted Protein Degradation through E2 Recruitment

ACS chemical biology, 2023-04, Vol.18 (4), p.897-904

2023

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Highly Diastereo- and Enantioselective Allylboration of Aldehydes using α‑Substituted Allyl/Crotyl Pinacol Boronic Esters via in Situ Generated Borinic Esters

Journal of the American Chemical Society, 2013-04, Vol.135 (14), p.5316-5319

2013

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A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core

Chemical science (Cambridge), 2020-10, Vol.11 (43), p.11897-1191

2020

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Highly Selective Allylborations of Aldehydes Using α,α-Disubstituted Allylic Pinacol Boronic Esters

Angewandte Chemie (International ed.), 2014-06, Vol.53 (24), p.6145-6149

2014

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Rational Chemical Design of Molecular Glue Degraders

ACS central science, 2023-05, Vol.9 (5), p.915-926

2023

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Discovery of Potent Pyrazoline‐Based Covalent SARS‐CoV‐2 Main Protease Inhibitors

Chembiochem : a European journal of chemical biology, 2023-06, Vol.24 (11), p.e202300116-n/a

2023

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Diastereodivergent Synthesis of Trisubstituted Alkenes through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone

Angewandte Chemie, 2012-12, Vol.124 (50), p.12612-12616

2012

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Highly Selective Allylborations of Aldehydes Using [alpha],[alpha]-Disubstituted Allylic Pinacol Boronic Esters

Angewandte Chemie International Edition, 2014-06, Vol.53 (24), p.6145-6149

International ed. in English, 2014

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Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenesElectronic supplementary information (ESI) available: Full experimental and characterisation data is provided. See DOI: 10.1039/c2cc32176a

2012-08

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ChemInform Abstract: Diastereodivergent Synthesis of Trisubstituted Alkenes Through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone

ChemInform, 2013-05, Vol.44 (20), p.no-no

2013

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Highly Selective Allylborations of Aldehydes Using α,α-Disubstituted Allylic Pinacol Boronic Esters

Angewandte Chemie, 2014-06, Vol.126 (24), p.6259-6263

2014

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Highly Selective Allylborations of Aldehydes Using [alpha],[alpha]-Disubstituted Allylic Pinacol Boronic Esters

Angewandte Chemie, 2014-06, Vol.126 (24), p.6259-6263

2014

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ChemInform Abstract: Application of the Lithiation-Borylation Reaction to the Rapid and Enantioselective Synthesis of the Bisabolane Family of Sesquiterpenes

ChemInform, 2013-01, Vol.44 (2), p.no-no

2013

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ChemInform Abstract: Highly Selective Allylborations of Aldehydes Using α,α-Disubstituted Allylic Pinacol Boronic Esters

ChemInform, 2014-12, Vol.45 (49), p.no-no

2014

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ChemInform Abstract: Highly Selective Allylborations of Aldehydes Using [alpha],[alpha]-Disubstituted Allylic Pinacol Boronic Esters

ChemInform, 2014-12, Vol.45 (49)

2014

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ChemInform Abstract: Highly Diastereo- and Enantioselective Allylboration of Aldehydes Using [alpha]-Substituted Allyl/Crotyl Pinacol Boronic Esters via in situ Generated Borinic Esters

ChemInform, 2013-09, Vol.44 (38)

2013

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ChemInform Abstract: Highly Diastereo- and Enantioselective Allylboration of Aldehydes Using α-Substituted Allyl/Crotyl Pinacol Boronic Esters via in situ Generated Borinic Esters

ChemInform, 2013-09, Vol.44 (38), p.no-no

2013

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Emergence of the Asian 1 genotype of dengue virus serotype 2 in viet nam: in vivo fitness advantage and lineage replacement in South-East Asia

PLoS neglected tropical diseases, 2010-07, Vol.4 (7), p.e757

2010

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Haro 11: The Spatially Resolved Lyman Continuum Sources

The Astrophysical journal, 2024-06, Vol.967 (2), p.117

2024

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Enantioselective Rhodium(III)-Catalyzed Markovnikov Hydroboration of Unactivated Terminal Alkenes

Diastereodivergent Synthesis of Trisubstituted Alkenes through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone

Deubiquitinase-targeting chimeras for targeted protein stabilization

Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes

Correction to “Rational Chemical Design of Molecular Glue Degraders”

Property-Based Drug Design Merits a Nobel Prize

Targeted Protein Degradation through E2 Recruitment

Highly Diastereo- and Enantioselective Allylboration of Aldehydes using α‑Substituted Allyl/Crotyl Pinacol Boronic Esters via in Situ Generated Borinic Esters

A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core

Highly Selective Allylborations of Aldehydes Using α,α-Disubstituted Allylic Pinacol Boronic Esters

Rational Chemical Design of Molecular Glue Degraders

Discovery of Potent Pyrazoline‐Based Covalent SARS‐CoV‐2 Main Protease Inhibitors

Diastereodivergent Synthesis of Trisubstituted Alkenes through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone

Highly Selective Allylborations of Aldehydes Using [alpha],[alpha]-Disubstituted Allylic Pinacol Boronic Esters

Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenesElectronic supplementary information (ESI) available: Full experimental and characterisation data is provided. See DOI: 10.1039/c2cc32176a

ChemInform Abstract: Diastereodivergent Synthesis of Trisubstituted Alkenes Through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone

Highly Selective Allylborations of Aldehydes Using α,α-Disubstituted Allylic Pinacol Boronic Esters

Highly Selective Allylborations of Aldehydes Using [alpha],[alpha]-Disubstituted Allylic Pinacol Boronic Esters

ChemInform Abstract: Application of the Lithiation-Borylation Reaction to the Rapid and Enantioselective Synthesis of the Bisabolane Family of Sesquiterpenes

ChemInform Abstract: Highly Selective Allylborations of Aldehydes Using α,α-Disubstituted Allylic Pinacol Boronic Esters

ChemInform Abstract: Highly Selective Allylborations of Aldehydes Using [alpha],[alpha]-Disubstituted Allylic Pinacol Boronic Esters

ChemInform Abstract: Highly Diastereo- and Enantioselective Allylboration of Aldehydes Using [alpha]-Substituted Allyl/Crotyl Pinacol Boronic Esters via in situ Generated Borinic Esters

ChemInform Abstract: Highly Diastereo- and Enantioselective Allylboration of Aldehydes Using α-Substituted Allyl/Crotyl Pinacol Boronic Esters via in situ Generated Borinic Esters

Emergence of the Asian 1 genotype of dengue virus serotype 2 in viet nam: in vivo fitness advantage and lineage replacement in South-East Asia

Haro 11: The Spatially Resolved Lyman Continuum Sources

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