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Cobalt-Catalyzed C–H Cyanation of (Hetero)arenes and 6‑Arylpurines with N‑Cyanosuccinimide as a New Cyanating Agent

Organic letters, 2015-02, Vol.17 (3), p.660-663

2015

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Redox-neutral C-H annulation strategies for the synthesis of heterocycles via high-valent CpCo(III) catalysis

Organic & biomolecular chemistry, 2023-05, Vol.21 (19), p.3918-3941

2023

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Catalytic cyanation of aryl iodides using DMF and ammonium bicarbonate as the combined source of cyanide: a dual role of copper catalysts

Chemical communications (Cambridge, England), 2014-01, Vol.50 (4), p.448-450

2014

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CpIr()-catalyzed C-H/N-H functionalization of sulfoximines for the synthesis of 1,2-benzothiazines at room temperature

Chemical communications (Cambridge, England), 2018-06, Vol.54 (49), p.6288-6291

2018

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Promising efficacy and acceptable safety of venetoclax plus bortezomib and dexamethasone in relapsed/refractory MM

Blood, 2017-11, Vol.130 (22), p.2392-2400

2017

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CpCo()-catalyzed C-H amination/annulation cascade of sulfoxonium ylides with anthranils for the synthesis of indoloindolones

Chemical communications (Cambridge, England), 2021-07, Vol.57 (58), p.7164-7167

2021

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Arylidene and amino spacer‐linked rhodanine‐quinoline hybrids as upgraded antimicrobial agents

Chemical biology & drug design, 2023-12, Vol.102 (6), p.1632-1642

2023

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Ru(II)-Catalyzed Regioselective Redox-Neutral [4 + 2] Annulation of N‑Chlorobenzamides with 1,3-Diynes at Room Temperature for the Synthesis of Isoquinolones

Journal of organic chemistry, 2023-04, Vol.88 (7), p.4704-4719

2023

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Applications of copper and iron-catalyzed Csp3-Csp3 cross-dehydrogenative coupling in organic synthesis

Synthetic communications, 2023-10, Vol.53 (20), p.1665-1700

2023

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Deciphering the Origin of Regioselectivity in Ru(II)-Catalyzed C–H Annulation of N‑Chlorobenzamides with 1,3-Diynes

Journal of organic chemistry, 2024-05, Vol.89 (10), p.6838-6846

2024

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Reverse Regioselective CpCo(III)-Catalyzed [4 + 2] C–H Annulation of N‑Chloroamides with Vinylsilanes: Synthesis of 4‑Silylated Isoquinolones and Their Synthetic Utilities

Organic letters, 2023-11, Vol.25 (43), p.7878-7883

2023

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Tri‐substituted 1,3,5‐triazine‐based analogs as effective HIV‐1 non‐nucleoside reverse transcriptase inhibitors (NNRTIs): A systematic review

Drug development research, 2024-02, Vol.85 (1), p.e22154-n/a

2024

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Advances in transition metal-catalyzed C-H amination strategies using anthranils

Organic & biomolecular chemistry, 2023-11, Vol.21 (44), p.8794-8812

2023

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Catalyst- and reagent-free 1,6-hydrophosphonylation of p-quinone methides: a practical approach for the synthesis of diarylmethyl phosphine oxides

Organic & biomolecular chemistry, 2019-08, Vol.17 (32), p.7536-7546

2019

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Phase II Study of Alisertib, a Selective Aurora A Kinase Inhibitor, in Relapsed and Refractory Aggressive B- and T-Cell Non-Hodgkin Lymphomas

Journal of clinical oncology, 2014-01, Vol.32 (1), p.44-50

2014

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Free Amine-Directed Ru(II)-Catalyzed Redox-Neutral [4 + 2] C–H Activation/Annulation of Benzylamines with Sulfoxonium Ylides

Journal of organic chemistry, 2022-10, Vol.87 (19), p.12608-12621

2022

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Total Synthesis of Lamellarin D Trimethyl Ether, Lamellarin D, and Lamellarin H

Journal of organic chemistry, 2017-05, Vol.82 (9), p.4998-5004

2017

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Randomized Phase III Noninferiority Study Comparing Two Radiotherapy Fractionation Schedules in Patients With Low-Risk Prostate Cancer

Journal of clinical oncology, 2016-07, Vol.34 (20), p.2325-2332

2016

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Cobalt(III)-catalyzed C-H halogenation of 6-arylpurines: facile entry into arylated, sulfenylated and alkoxylated 6-arylpurines

Organic & biomolecular chemistry, 2016-01, Vol.14 (12), p.3275-3283

2016

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CpCo(III)-Catalyzed C–H/N–N Functionalization of Arylhydrazones for the Synthesis of Isoquinolines

Journal of organic chemistry, 2016-11, Vol.81 (22), p.11409-11415

2016

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Indole Fused Benzimidazole Hybrids: A Promising Combination to Fulfill Pharmacological Significance

Polycyclic aromatic compounds, 2023-10, Vol.43 (9), p.7783-7807

2023

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CpCo(III)-Catalyzed C–H Functionalization Cascade of N‑Methoxyamides with Alkynedione for the Synthesis of Indolizidines

Organic letters, 2017-04, Vol.19 (8), p.2186-2189

2017

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Investigation of the antibacterial activity of new quinazoline derivatives against methicillin and quinolone resistant Staphylococcus aureus

Journal of chemical research, 2020-05, Vol.44 (5-6), p.315-321

Patel, Amit B

2020

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CpIr(III)-Catalyzed C–H/O–H Functionalization of Salicylaldehydes for the Synthesis of Chromones at Room Temperature

Journal of organic chemistry, 2019-07, Vol.84 (14), p.9188-9195

2019

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Review on NAD(P)H dehydrogenase quinone 1 (NQO1) pathway

Molecular biology reports, 2022-09, Vol.49 (9), p.8907-8924

2022

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Cobalt-Catalyzed C–H Cyanation of (Hetero)arenes and 6‑Arylpurines with N‑Cyanosuccinimide as a New Cyanating Agent

Redox-neutral C-H annulation strategies for the synthesis of heterocycles via high-valent CpCo(III) catalysis

Catalytic cyanation of aryl iodides using DMF and ammonium bicarbonate as the combined source of cyanide: a dual role of copper catalysts

CpIr()-catalyzed C-H/N-H functionalization of sulfoximines for the synthesis of 1,2-benzothiazines at room temperature

Promising efficacy and acceptable safety of venetoclax plus bortezomib and dexamethasone in relapsed/refractory MM

CpCo()-catalyzed C-H amination/annulation cascade of sulfoxonium ylides with anthranils for the synthesis of indoloindolones

Arylidene and amino spacer‐linked rhodanine‐quinoline hybrids as upgraded antimicrobial agents

Ru(II)-Catalyzed Regioselective Redox-Neutral [4 + 2] Annulation of N‑Chlorobenzamides with 1,3-Diynes at Room Temperature for the Synthesis of Isoquinolones

Applications of copper and iron-catalyzed Csp3-Csp3 cross-dehydrogenative coupling in organic synthesis

Deciphering the Origin of Regioselectivity in Ru(II)-Catalyzed C–H Annulation of N‑Chlorobenzamides with 1,3-Diynes

Reverse Regioselective CpCo(III)-Catalyzed [4 + 2] C–H Annulation of N‑Chloroamides with Vinylsilanes: Synthesis of 4‑Silylated Isoquinolones and Their Synthetic Utilities

Tri‐substituted 1,3,5‐triazine‐based analogs as effective HIV‐1 non‐nucleoside reverse transcriptase inhibitors (NNRTIs): A systematic review

Advances in transition metal-catalyzed C-H amination strategies using anthranils

Catalyst- and reagent-free 1,6-hydrophosphonylation of p-quinone methides: a practical approach for the synthesis of diarylmethyl phosphine oxides

Phase II Study of Alisertib, a Selective Aurora A Kinase Inhibitor, in Relapsed and Refractory Aggressive B- and T-Cell Non-Hodgkin Lymphomas

Free Amine-Directed Ru(II)-Catalyzed Redox-Neutral [4 + 2] C–H Activation/Annulation of Benzylamines with Sulfoxonium Ylides

Total Synthesis of Lamellarin D Trimethyl Ether, Lamellarin D, and Lamellarin H

Randomized Phase III Noninferiority Study Comparing Two Radiotherapy Fractionation Schedules in Patients With Low-Risk Prostate Cancer

Cobalt(III)-catalyzed C-H halogenation of 6-arylpurines: facile entry into arylated, sulfenylated and alkoxylated 6-arylpurines

CpCo(III)-Catalyzed C–H/N–N Functionalization of Arylhydrazones for the Synthesis of Isoquinolines

Indole Fused Benzimidazole Hybrids: A Promising Combination to Fulfill Pharmacological Significance

CpCo(III)-Catalyzed C–H Functionalization Cascade of N‑Methoxyamides with Alkynedione for the Synthesis of Indolizidines

Investigation of the antibacterial activity of new quinazoline derivatives against methicillin and quinolone resistant Staphylococcus aureus

CpIr(III)-Catalyzed C–H/O–H Functionalization of Salicylaldehydes for the Synthesis of Chromones at Room Temperature

Review on NAD(P)H dehydrogenase quinone 1 (NQO1) pathway

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