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Rh(III)/Cu(II)-cocatalyzed synthesis of 1H-indazoles through C-H amidation and N-N bond formation

Journal of the American Chemical Society, 2013-06, Vol.135 (24), p.8802-8805

2013

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Unparalleled Ease of Access to a Library of Biheteroaryl Fluorophores via Oxidative Cross-Coupling Reactions: Discovery of Photostable NIR Probe for Mitochondria

Journal of the American Chemical Society, 2016-04, Vol.138 (14), p.4730-4738

2016

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Recent Advances in Indazole-Containing Derivatives: Synthesis and Biological Perspectives

Molecules (Basel, Switzerland), 2018-10, Vol.23 (11), p.2783

2018

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Copper-Catalyzed Aerobic C(sp2)–H Functionalization for C–N Bond Formation: Synthesis of Pyrazoles and Indazoles

Journal of organic chemistry, 2013-04, Vol.78 (8), p.3636-3646

2013

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Rhodium(III)-Catalyzed Indazole Synthesis by C–H Bond Functionalization and Cyclative Capture

Journal of the American Chemical Society, 2013-05, Vol.135 (19), p.7122-7125

2013

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Synthesis of indazole motifs and their medicinal importance: An overview

European journal of medicinal chemistry, 2015-01, Vol.90, p.707-731

2015

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Highly Enantioselective Synthesis of Indazoles with a C3-Quaternary Chiral Center Using CuH Catalysis

Journal of the American Chemical Society, 2020-06, Vol.142 (23), p.10550-10556

2020

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P III /P V ═O-Catalyzed Intermolecular N-N Bond Formation: Cross-Selective Reductive Coupling of Nitroarenes and Anilines

Journal of the American Chemical Society, 2021-09, Vol.143 (36), p.14464-14469

2021

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Selective Inhibitors of G2019S-LRRK2 Kinase Activity

Journal of medicinal chemistry, 2020-12, Vol.63 (23), p.14821-14839

2020

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Discovery and Preclinical Characterization of 6‑Chloro-5-[4-(1-hydroxycyclobutyl)phenyl]‑1H‑indole-3-carboxylic Acid (PF-06409577), a Direct Activator of Adenosine Monophosphate-activated Protein Kinase (AMPK), for the Potential Treatment of Diabetic Nephropathy

Journal of medicinal chemistry, 2016-09, Vol.59 (17), p.8068-8081

2016

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Pyrimido[1,2-b]indazole derivatives: Selective inhibitors of human monoamine oxidase B with neuroprotective activity

European journal of medicinal chemistry, 2021-01, Vol.209, p.112911-112911, Article 112911

2021

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Copper-Catalyzed C(sp2)–H Amidation with Azides as Amino Sources

Organic letters, 2014-09, Vol.16 (18), p.4702-4705

2014

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Regioselective Synthesis of 2H‑Indazoles Using a Mild, One-Pot Condensation–Cadogan Reductive Cyclization

Organic letters, 2014-06, Vol.16 (11), p.3114-3117

2014

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Chemistry and biology of indoles and indazoles: a mini-review

Mini reviews in medicinal chemistry, 2013-10, Vol.13 (12), p.1792-1800

2013

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Consecutive Condensation, C–N and N–N Bond Formations: A Copper- Catalyzed One-Pot Three-Component Synthesis of 2H-Indazole

Organic letters, 2011-07, Vol.13 (13), p.3542-3545

2011

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Direct Arylations of 2H-Indazoles On Water

Organic letters, 2010-01, Vol.12 (2), p.224-226

2010

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Indazole- and Indole-5-carboxamides: Selective and Reversible Monoamine Oxidase B Inhibitors with Subnanomolar Potency

Journal of medicinal chemistry, 2014-08, Vol.57 (15), p.6679-6703

2014

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Access to 3‑Acyl-(2H)‑indazoles via Rh(III)-Catalyzed C–H Addition and Cyclization of Azobenzenes with α‑Keto Aldehydes

Organic letters, 2016-01, Vol.18 (2), p.232-235

2016

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CF3 Derivatives of the Anticancer Ru(III) Complexes KP1019, NKP-1339, and Their Imidazole and Pyridine Analogues Show Enhanced Lipophilicity, Albumin Interactions, and Cytotoxicity

Inorganic chemistry, 2016-05, Vol.55 (10), p.4850-4863

2016

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Intramolecular Fe(II)-Catalyzed N−O or N−N Bond Formation from Aryl Azides

Organic letters, 2010-06, Vol.12 (12), p.2884-2887

2010

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Palladium-Catalyzed Oxidative Direct C3- and C7-Alkenylations of Indazoles: Application to the Synthesis of Gamendazole

Organic letters, 2015-09, Vol.17 (17), p.4320-4323

2015

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Pharmacology of Indole and Indazole Synthetic Cannabinoid Designer Drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB-PINACA, ADBICA, and 5F-ADBICA

ACS chemical neuroscience, 2015-09, Vol.6 (9), p.1546-1559

2015

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Synthesis of 3-Substituted Indazoles from Arynes and N-Tosylhydrazones

Organic letters, 2011-07, Vol.13 (13), p.3340-3343

2011

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Synthesis of 2H-Indazoles by the [3 + 2] Cycloaddition of Arynes and Sydnones

Organic letters, 2010-05, Vol.12 (10), p.2234-2237

2010

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Design and Synthesis of a Pan-Janus Kinase Inhibitor Clinical Candidate (PF-06263276) Suitable for Inhaled and Topical Delivery for the Treatment of Inflammatory Diseases of the Lungs and Skin

Journal of medicinal chemistry, 2017-01, Vol.60 (2), p.767-786

2017

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Rh(III)/Cu(II)-cocatalyzed synthesis of 1H-indazoles through C-H amidation and N-N bond formation

Unparalleled Ease of Access to a Library of Biheteroaryl Fluorophores via Oxidative Cross-Coupling Reactions: Discovery of Photostable NIR Probe for Mitochondria

Recent Advances in Indazole-Containing Derivatives: Synthesis and Biological Perspectives

Copper-Catalyzed Aerobic C(sp2)–H Functionalization for C–N Bond Formation: Synthesis of Pyrazoles and Indazoles

Rhodium(III)-Catalyzed Indazole Synthesis by C–H Bond Functionalization and Cyclative Capture

Synthesis of indazole motifs and their medicinal importance: An overview

Highly Enantioselective Synthesis of Indazoles with a C3-Quaternary Chiral Center Using CuH Catalysis

P III /P V ═O-Catalyzed Intermolecular N-N Bond Formation: Cross-Selective Reductive Coupling of Nitroarenes and Anilines

Selective Inhibitors of G2019S-LRRK2 Kinase Activity

Discovery and Preclinical Characterization of 6‑Chloro-5-[4-(1-hydroxycyclobutyl)phenyl]‑1H‑indole-3-carboxylic Acid (PF-06409577), a Direct Activator of Adenosine Monophosphate-activated Protein Kinase (AMPK), for the Potential Treatment of Diabetic Nephropathy

Pyrimido[1,2-b]indazole derivatives: Selective inhibitors of human monoamine oxidase B with neuroprotective activity

Copper-Catalyzed C(sp2)–H Amidation with Azides as Amino Sources

Regioselective Synthesis of 2H‑Indazoles Using a Mild, One-Pot Condensation–Cadogan Reductive Cyclization

Chemistry and biology of indoles and indazoles: a mini-review

Consecutive Condensation, C–N and N–N Bond Formations: A Copper- Catalyzed One-Pot Three-Component Synthesis of 2H-Indazole

Direct Arylations of 2H-Indazoles On Water

Indazole- and Indole-5-carboxamides: Selective and Reversible Monoamine Oxidase B Inhibitors with Subnanomolar Potency

Access to 3‑Acyl-(2H)‑indazoles via Rh(III)-Catalyzed C–H Addition and Cyclization of Azobenzenes with α‑Keto Aldehydes

CF3 Derivatives of the Anticancer Ru(III) Complexes KP1019, NKP-1339, and Their Imidazole and Pyridine Analogues Show Enhanced Lipophilicity, Albumin Interactions, and Cytotoxicity

Intramolecular Fe(II)-Catalyzed N−O or N−N Bond Formation from Aryl Azides

Palladium-Catalyzed Oxidative Direct C3- and C7-Alkenylations of Indazoles: Application to the Synthesis of Gamendazole

Pharmacology of Indole and Indazole Synthetic Cannabinoid Designer Drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB-PINACA, ADBICA, and 5F-ADBICA

Synthesis of 3-Substituted Indazoles from Arynes and N-Tosylhydrazones

Synthesis of 2H-Indazoles by the [3 + 2] Cycloaddition of Arynes and Sydnones

Design and Synthesis of a Pan-Janus Kinase Inhibitor Clinical Candidate (PF-06263276) Suitable for Inhaled and Topical Delivery for the Treatment of Inflammatory Diseases of the Lungs and Skin

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