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Conazoles

Molecules, 2010-06, Vol.15 (6), p.4129-4188

2010

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Access to Silylated Pyrazole Derivatives by Palladium-Catalyzed C−H Activation of a TMS group

Chemistry : a European journal, 2016-07, Vol.22 (28), p.9687-9692

2016

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Cobalt-Catalyzed Diastereoselective Synthesis of C‑Furanosides. Total Synthesis of (−)-Isoaltholactone

Journal of organic chemistry, 2013-12, Vol.78 (23), p.11807-11814

2013

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Iron-Catalyzed Synthesis of C2 Aryl- and N‑Heteroaryl-Substituted Tetrahydropyrans

Journal of organic chemistry, 2015-12, Vol.80 (24), p.12509-12525

2015

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Tandem Suzuki-Miyaura Coupling/Acid-Catalyzed Cyclization between Vinyl Ether Boronates and Vinyl Halides: A Concise Approach to Polysubstituted Furans

Organic letters, 2013-08, Vol.15 (15), p.3840-3843

2013

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FEP+ calculations predict a stereochemical SAR switch for first-in-class indoline NIK inhibitors for multiple myeloma

Future drug discovery, 2020-07, Vol.2 (3)

2020

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Direct α-Functionalization of Saturated Cyclic Amines

Chemistry : a European journal, 2012-08, Vol.18 (33), p.10092-10142

2012

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Diastereoselective Metal-Catalyzed Synthesis of C-Aryl and C-Vinyl Glycosides

Angewandte Chemie (International ed.), 2012-10, Vol.51 (44), p.11101-11104

International ed. in English, 2012

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The Novel Azole R126638 Is a Selective Inhibitor of Ergosterol Synthesis in Candida albicans, Trichophyton spp., and Microsporum canis

Antimicrobial Agents and Chemotherapy, 2004-09, Vol.48 (9), p.3272-3278

2004

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C-2 Arylation of Piperidines through Directed Transition-Metal-Catalyzed sp3 CH Activation

Chemistry : a European journal, 2010-11, Vol.16 (44), p.13063-13067

2010

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Organic glasses with tunable liquid-crystalline order through kinetic arrest of end-over-end rotation: the case of saperconazole

Soft matter, 2020-02, Vol.16 (8), p.225-23

2020

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Minisci-Photoredox-Mediated α‑Heteroarylation of N‑Protected Secondary Amines: Remarkable Selectivity of Azetidines

Organic letters, 2018-10, Vol.20 (19), p.6003-6006

2018

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Stereodivergent Synthesis of Biologically Active Spironucleoside Scaffolds via Catalytic Cyclopropanation of 4-exo-Methylene Furanosides

Journal of organic chemistry, 2021-12, Vol.86 (23), p.17344-17361

2021

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Synthesis and Reactivity of Spirocarbocycles as Scaffolds for Nucleoside Analogues

Journal of organic chemistry, 2020-12, Vol.85 (23), p.14989-15005

2020

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Synthesis and transformations of pyrrolo[1,2-a][1,3,5]-triazines

Tetrahedron letters, 2018-12, Vol.59 (52), p.4537-4539

2018

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Correction to “Regio- and Stereoselective Synthesis of C‑4′ Spirocyclobutyl Ribofuranose Scaffolds and Their Use as Biologically Active Nucleoside Analogues”

Organic letters, 2022-01, Vol.24 (2), p.798-798

2022

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Iron-Catalyzed Synthesis of Sulfur-Containing Heterocycles

Journal of organic chemistry, 2017-04, Vol.82 (8), p.4020-4036

2017

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Discovery and Pharmacological Characterization of JNJ-64619178, a Novel Small-Molecule Inhibitor of PRMT5 with Potent Antitumor Activity

Molecular cancer therapeutics, 2021-12, Vol.20 (12), p.2317-2328

2021

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Discovery of JNJ-63576253: A Clinical Stage Androgen Receptor Antagonist for F877L Mutant and Wild-Type Castration-Resistant Prostate Cancer (mCRPC)

Journal of medicinal chemistry, 2021-01, Vol.64 (2), p.909-924

2021

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Preparation of 4′‐Spirocyclobutyl Nucleoside Analogues as Novel and Versatile Adenosine Scaffolds

Chemistry : a European journal, 2019-12, Vol.25 (67), p.15419-15423

2019

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Anionic Access to Silylated and Germylated Binuclear Heterocycles

Chemistry : a European journal, 2014-08, Vol.20 (32), p.10131-10139

2014

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Discovery and optimization of a series of small-molecule allosteric inhibitors of MALT1 protease

Bioorganic & medicinal chemistry letters, 2019-12, Vol.29 (23), p.126743-126743, Article 126743

2019

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Ruthenium‐Catalyzed Reductive Arylation of N‐(2‐Pyridinyl)amides with Isopropanol and Arylboronate Esters

Angewandte Chemie (International ed.), 2019-01, Vol.58 (2), p.482-487

International ed. in English, 2019

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Chemoselective Palladium‐Catalyzed Direct C–H Arylation of 5‐Carboxyimidazoles: Unparalleled Access to Fused Imidazole‐Based Tricycles Containing Six‐, Seven‐ or Eight‐Membered Rings

European journal of organic chemistry, 2017-05, Vol.2017 (17), p.2491-2494

2017

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Design and synthesis of a series of bioavailable fatty acid synthase (FASN) KR domain inhibitors for cancer therapy

Bioorganic & medicinal chemistry letters, 2018-07, Vol.28 (12), p.2159-2164

2018

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Conazoles

Access to Silylated Pyrazole Derivatives by Palladium-Catalyzed C−H Activation of a TMS group

Cobalt-Catalyzed Diastereoselective Synthesis of C‑Furanosides. Total Synthesis of (−)-Isoaltholactone

Iron-Catalyzed Synthesis of C2 Aryl- and N‑Heteroaryl-Substituted Tetrahydropyrans

Tandem Suzuki-Miyaura Coupling/Acid-Catalyzed Cyclization between Vinyl Ether Boronates and Vinyl Halides: A Concise Approach to Polysubstituted Furans

FEP+ calculations predict a stereochemical SAR switch for first-in-class indoline NIK inhibitors for multiple myeloma

Direct α-Functionalization of Saturated Cyclic Amines

Diastereoselective Metal-Catalyzed Synthesis of C-Aryl and C-Vinyl Glycosides

The Novel Azole R126638 Is a Selective Inhibitor of Ergosterol Synthesis in Candida albicans, Trichophyton spp., and Microsporum canis

C-2 Arylation of Piperidines through Directed Transition-Metal-Catalyzed sp3 CH Activation

Organic glasses with tunable liquid-crystalline order through kinetic arrest of end-over-end rotation: the case of saperconazole

Minisci-Photoredox-Mediated α‑Heteroarylation of N‑Protected Secondary Amines: Remarkable Selectivity of Azetidines

Stereodivergent Synthesis of Biologically Active Spironucleoside Scaffolds via Catalytic Cyclopropanation of 4-exo-Methylene Furanosides

Synthesis and Reactivity of Spirocarbocycles as Scaffolds for Nucleoside Analogues

Synthesis and transformations of pyrrolo[1,2-a][1,3,5]-triazines

Correction to “Regio- and Stereoselective Synthesis of C‑4′ Spirocyclobutyl Ribofuranose Scaffolds and Their Use as Biologically Active Nucleoside Analogues”

Iron-Catalyzed Synthesis of Sulfur-Containing Heterocycles

Discovery and Pharmacological Characterization of JNJ-64619178, a Novel Small-Molecule Inhibitor of PRMT5 with Potent Antitumor Activity

Discovery of JNJ-63576253: A Clinical Stage Androgen Receptor Antagonist for F877L Mutant and Wild-Type Castration-Resistant Prostate Cancer (mCRPC)

Preparation of 4′‐Spirocyclobutyl Nucleoside Analogues as Novel and Versatile Adenosine Scaffolds

Anionic Access to Silylated and Germylated Binuclear Heterocycles

Discovery and optimization of a series of small-molecule allosteric inhibitors of MALT1 protease

Ruthenium‐Catalyzed Reductive Arylation of N‐(2‐Pyridinyl)amides with Isopropanol and Arylboronate Esters

Chemoselective Palladium‐Catalyzed Direct C–H Arylation of 5‐Carboxyimidazoles: Unparalleled Access to Fused Imidazole‐Based Tricycles Containing Six‐, Seven‐ or Eight‐Membered Rings

Design and synthesis of a series of bioavailable fatty acid synthase (FASN) KR domain inhibitors for cancer therapy

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