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Nazarov Cyclization of Divinyl and Arylvinyl Epoxides: Application in the Synthesis of Resveratrol-Based Natural Products

Chemistry : a European journal, 2015-04, Vol.21 (17), p.6475-6480

2015

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Structure-Based Design of Highly Potent HIV‑1 Protease Inhibitors Containing New Tricyclic Ring P2-Ligands: Design, Synthesis, Biological, and X‑ray Structural Studies

Journal of medicinal chemistry, 2020-05, Vol.63 (9), p.4867-4879

2020

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Enantioselective Synthesis of a Cyclopropane Derivative of Spliceostatin A and Evaluation of Bioactivity

Organic letters, 2018-11, Vol.20 (22), p.7293-7297

2018

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Potent HIV-1 protease inhibitors incorporating squaramide-derived P2 ligands: Design, synthesis, and biological evaluation

Bioorganic & medicinal chemistry letters, 2019-09, Vol.29 (18), p.2565-2570

2019

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Chloropyridinyl Esters of Nonsteroidal Anti-Inflammatory Agents and Related Derivatives as Potent SARS-CoV-2 3CL Protease Inhibitors

Molecules (Basel, Switzerland), 2021-09, Vol.26 (19), p.5782

2021

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Potent HIV‐1 Protease Inhibitors Containing Carboxylic and Boronic Acids: Effect on Enzyme Inhibition and Antiviral Activity and Protein‐Ligand X‐ray Structural Studies

ChemMedChem, 2019-11, Vol.14 (21), p.1863-1872

2019

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Design, Synthesis and X‐Ray Structural Studies of Potent HIV‐1 Protease Inhibitors Containing C‐4 Substituted Tricyclic Hexahydro‐Furofuran Derivatives as P2 Ligands

ChemMedChem, 2022-05, Vol.17 (9), p.e202200058-n/a

2022

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Design, synthesis, and X-ray studies of potent HIV-1 protease inhibitors incorporating aminothiochromane and aminotetrahydronaphthalene carboxamide derivatives as the P2 ligands

European journal of medicinal chemistry, 2018-12, Vol.160 (C), p.171-182

2018

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Total Synthesis and Absolute Configuration of Curvularides A‑E

Journal of organic chemistry, 2012-11, Vol.77 (22), p.10010-10020

2012

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SARS-CoV-2 papain-like protease (PLpro) inhibitory and antiviral activity of small molecule derivatives for drug leads

Bioorganic & medicinal chemistry letters, 2023-11, Vol.96, p.129489-129489, Article 129489

2023

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Synthesis of diversely substituted quinazoline-2,4(1 H ,3 H )-diones by cyclization of tert -butyl (2-cyanoaryl)carbamates

Organic & biomolecular chemistry, 2024-01, Vol.22 (32), p.6495-6499

2024

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Asymmetric Diels-Alder reaction of 3-(acyloxy)acryloyl oxazolidinones: optically active synthesis of a high-affinity ligand for potent HIV-1 protease inhibitors

RSC advances, 2019, Vol.9 (71), p.41755-41763

2019

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Exploration of imatinib and nilotinib-derived templates as the P2-Ligand for HIV-1 protease inhibitors: Design, synthesis, protein X-ray structural studies, and biological evaluation

European journal of medicinal chemistry, 2023-07, Vol.255 (C), p.115385-115385, Article 115385

2023

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Design and Synthesis of Highly Potent HIV‑1 Protease Inhibitors Containing Tricyclic Fused Ring Systems as Novel P2 Ligands: Structure–Activity Studies, Biological and X‑ray Structural Analysis

Journal of medicinal chemistry, 2018-05, Vol.61 (10), p.4561-4577

2018

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Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants

ChemMedChem, 2018-04, Vol.13 (8), p.803-815

2018

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Highly Selective and Potent Human β‐Secretase 2 (BACE2) Inhibitors against Type 2 Diabetes: Design, Synthesis, X‐ray Structure and Structure–Activity Relationship Studies

ChemMedChem, 2019-03, Vol.14 (5), p.545-560

2019

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Design, Synthesis, and X‑ray Studies of Potent HIV‑1 Protease Inhibitors with P2-Carboxamide Functionalities

ACS medicinal chemistry letters, 2020-10, Vol.11 (10), p.1965-1972

2020

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Cover Feature: Highly Selective and Potent Human β‐Secretase 2 (BACE2) Inhibitors against Type 2 Diabetes: Design, Synthesis, X‐ray Structure and Structure–Activity Relationship Studies (ChemMedChem 5/2019)

ChemMedChem, 2019-03, Vol.14 (5), p.513-513

2019

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Front Cover: Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants (ChemMedChem 8/2018)

ChemMedChem, 2018-04, Vol.13 (8), p.762-762

2018

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Two new diterpenoids from the roots of Pygmacopremna herbacea

Phytochemistry letters, 2015-06, Vol.12, p.129-132

2015

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ChemInform Abstract: Nazarov Cyclization of Divinyl and Arylvinyl Epoxides: Application in the Synthesis of Resveratrol-Based Natural Products

ChemInform, 2015-09, Vol.46 (36), p.no-no

2015

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Nazarov Cyclization of Divinyl and Arylvinyl Epoxides: Application in the Synthesis of Resveratrol-Based Natural Products

Structure-Based Design of Highly Potent HIV‑1 Protease Inhibitors Containing New Tricyclic Ring P2-Ligands: Design, Synthesis, Biological, and X‑ray Structural Studies

Enantioselective Synthesis of a Cyclopropane Derivative of Spliceostatin A and Evaluation of Bioactivity

Potent HIV-1 protease inhibitors incorporating squaramide-derived P2 ligands: Design, synthesis, and biological evaluation

Chloropyridinyl Esters of Nonsteroidal Anti-Inflammatory Agents and Related Derivatives as Potent SARS-CoV-2 3CL Protease Inhibitors

Potent HIV‐1 Protease Inhibitors Containing Carboxylic and Boronic Acids: Effect on Enzyme Inhibition and Antiviral Activity and Protein‐Ligand X‐ray Structural Studies

Design, Synthesis and X‐Ray Structural Studies of Potent HIV‐1 Protease Inhibitors Containing C‐4 Substituted Tricyclic Hexahydro‐Furofuran Derivatives as P2 Ligands

Design, synthesis, and X-ray studies of potent HIV-1 protease inhibitors incorporating aminothiochromane and aminotetrahydronaphthalene carboxamide derivatives as the P2 ligands

Total Synthesis and Absolute Configuration of Curvularides A‑E

SARS-CoV-2 papain-like protease (PLpro) inhibitory and antiviral activity of small molecule derivatives for drug leads

Synthesis of diversely substituted quinazoline-2,4(1 H ,3 H )-diones by cyclization of tert -butyl (2-cyanoaryl)carbamates

Asymmetric Diels-Alder reaction of 3-(acyloxy)acryloyl oxazolidinones: optically active synthesis of a high-affinity ligand for potent HIV-1 protease inhibitors

Exploration of imatinib and nilotinib-derived templates as the P2-Ligand for HIV-1 protease inhibitors: Design, synthesis, protein X-ray structural studies, and biological evaluation

Design and Synthesis of Highly Potent HIV‑1 Protease Inhibitors Containing Tricyclic Fused Ring Systems as Novel P2 Ligands: Structure–Activity Studies, Biological and X‑ray Structural Analysis

Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants

Highly Selective and Potent Human β‐Secretase 2 (BACE2) Inhibitors against Type 2 Diabetes: Design, Synthesis, X‐ray Structure and Structure–Activity Relationship Studies

Design, Synthesis, and X‑ray Studies of Potent HIV‑1 Protease Inhibitors with P2-Carboxamide Functionalities

Cover Feature: Highly Selective and Potent Human β‐Secretase 2 (BACE2) Inhibitors against Type 2 Diabetes: Design, Synthesis, X‐ray Structure and Structure–Activity Relationship Studies (ChemMedChem 5/2019)

Front Cover: Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants (ChemMedChem 8/2018)

Two new diterpenoids from the roots of Pygmacopremna herbacea

ChemInform Abstract: Nazarov Cyclization of Divinyl and Arylvinyl Epoxides: Application in the Synthesis of Resveratrol-Based Natural Products

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