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MLi-2, a Potent, Selective, and Centrally Active Compound for Exploring the Therapeutic Potential and Safety of LRRK2 Kinase Inhibition

The Journal of pharmacology and experimental therapeutics, 2015-12, Vol.355 (3), p.397

2015

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Solution to the C 3 –Arylation of Indazoles: Development of a Scalable Method

Organic letters, 2016-07, Vol.18 (13), p.3218-3221

2016

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Total Syntheses of the Assigned Structures of Lituarines B and C

Journal of the American Chemical Society, 2008-01, Vol.130 (2), p.422-423

2008

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The Leader's Role in Managing Change: Five Cases of Technology-Enabled Business Transformation

Global Business and Organizational Excellence, 2015-03, Vol.34 (3), p.28-42

Kumar Basu, Kallol

2015

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Solution to the C3–Arylation of Indazoles: Development of a Scalable Method

Organic letters, 2016-07, Vol.18 (13), p.3218-3221

2016

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Discovery of a 3‑(4-Pyrimidinyl) Indazole (MLi-2), an Orally Available and Selective Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitor that Reduces Brain Kinase Activity

Journal of medicinal chemistry, 2017-04, Vol.60 (7), p.2983-2992

2017

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Development of a stereoselective and scalable process for the preparation of a methylcyclobutanol-pyridyl ether

Bioorganic & medicinal chemistry, 2018-02, Vol.26 (4), p.938-944

2018

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Development of a Green and Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 4: Formylation–Cyclization as a Flow–Batch Process Leads to Significant Improvements in Process Mass Intensity (PMI) and CO Generated versus the Batch–Batch Process

Organic process research & development, 2020-11, Vol.24 (11), p.2478-2490

2020

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Development of a Green and Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 1: Introduction and Process Overview

Organic process research & development, 2020-11, Vol.24 (11), p.2445-2452

2020

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Total Synthesis of (−)-Okilactomycin

Journal of the American Chemical Society, 2007-12, Vol.129 (48), p.14872-14874

2007

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Development of a Green and Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 3: Development of a One-Pot Formylation–Cyclization Sequence to the Diaminopyrimidine Core

Organic process research & development, 2020-11, Vol.24 (11), p.2462-2477

2020

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Can We Make Small Molecules Lean? Optimization of a Highly Lipophilic TarO Inhibitor

Journal of medicinal chemistry, 2017-05, Vol.60 (9), p.3851-3865

2017

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Pyrazoloquinolines as PDE10A inhibitors: Discovery of a tool compound

Bioorganic & medicinal chemistry letters, 2012-02, Vol.22 (3), p.1335-1339

2012

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Evaluation of possible intramolecular [4+2] cycloaddition routes for assembling the central tetracyclic core of the potent marine antiinflammatory agent mangicol A

Tetrahedron, 2006-05, Vol.62 (22), p.5178-5194

2006

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Mono- and Bis-Acrolein Derivatives by Reliable and Efficient One-Step Methylenation of Aldehyde Precursors

Synthesis (Stuttgart), 2004-12, Vol.2004 (17), p.2841-2844

2004

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Comparative investigation of kinetic consequences associated with long-range electronic effects on catalytic ruthenium-promoted ring-closing metathesis

Tetrahedron letters, 2002-07, Vol.43 (31), p.5453-5456

2002

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ChemInform Abstract: Solution to the C 3 —Arylation of Indazoles: Development of a Scalable Method

ChemInform, 2016-11, Vol.47 (47)

2016

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Relative Rate Profile for Ring-Closing Metathesis of a Series of 1-Substituted 1,7-Octadienes as Promoted by a 4,5-Dihydroimidazol-2-ylidene-Coordinated Ruthenium Catalyst

Organic letters, 2003-03, Vol.5 (6), p.789-792

2003

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New aspects in ring closing metathesis reactions studies toward the synthesis of mangicol A

Basu, Kallol

2004

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ProQuest

Ruthenium-Promoted Ring-Closing Metathesis of Ene-Dienes. Competitive Intramolecular Regioselection as a Function of Chain Length

Advanced synthesis & catalysis, 2002-08, Vol.344 (6-7), p.615-618

2002

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ChemInform Abstract: Solution to the C3—Arylation of Indazoles: Development of a Scalable Method

ChemInform, 2016-11, Vol.47 (47), p.no-no

2016

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Systematic Analysis of the Intramolecular Competition Associated with the Ring Closing Metathesis of Ene-Diene Systems of Differing Chain Length with a Pair of Ruthenium Catalysts

Helvetica chimica acta, 2002-10, Vol.85 (10), p.3033-3051

2002

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ChemInform Abstract: Total Synthesis of (-)-Okilactomycin

ChemInform, 2008-05, Vol.39 (19), p.no-no

2008

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Mono- and Bis-Acrolein Derivatives by Reliable and Efficient One-Step Methylenation of Aldehyde Precursors

ChemInform, 2005-04, Vol.36 (16), p.no-no

2005

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ChemInform Abstract: Total Syntheses of the Assigned Structures of Lituarines B and C

ChemInform, 2008-05, Vol.39 (22), p.no-no

2008

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MLi-2, a Potent, Selective, and Centrally Active Compound for Exploring the Therapeutic Potential and Safety of LRRK2 Kinase Inhibition

Solution to the C 3 –Arylation of Indazoles: Development of a Scalable Method

Total Syntheses of the Assigned Structures of Lituarines B and C

The Leader's Role in Managing Change: Five Cases of Technology-Enabled Business Transformation

Solution to the C3–Arylation of Indazoles: Development of a Scalable Method

Discovery of a 3‑(4-Pyrimidinyl) Indazole (MLi-2), an Orally Available and Selective Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitor that Reduces Brain Kinase Activity

Development of a stereoselective and scalable process for the preparation of a methylcyclobutanol-pyridyl ether

Development of a Green and Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 4: Formylation–Cyclization as a Flow–Batch Process Leads to Significant Improvements in Process Mass Intensity (PMI) and CO Generated versus the Batch–Batch Process

Development of a Green and Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 1: Introduction and Process Overview

Total Synthesis of (−)-Okilactomycin

Development of a Green and Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 3: Development of a One-Pot Formylation–Cyclization Sequence to the Diaminopyrimidine Core

Can We Make Small Molecules Lean? Optimization of a Highly Lipophilic TarO Inhibitor

Pyrazoloquinolines as PDE10A inhibitors: Discovery of a tool compound

Evaluation of possible intramolecular [4+2] cycloaddition routes for assembling the central tetracyclic core of the potent marine antiinflammatory agent mangicol A

Mono- and Bis-Acrolein Derivatives by Reliable and Efficient One-Step Methylenation of Aldehyde Precursors

Comparative investigation of kinetic consequences associated with long-range electronic effects on catalytic ruthenium-promoted ring-closing metathesis

ChemInform Abstract: Solution to the C 3 —Arylation of Indazoles: Development of a Scalable Method

Relative Rate Profile for Ring-Closing Metathesis of a Series of 1-Substituted 1,7-Octadienes as Promoted by a 4,5-Dihydroimidazol-2-ylidene-Coordinated Ruthenium Catalyst

New aspects in ring closing metathesis reactions studies toward the synthesis of mangicol A

Ruthenium-Promoted Ring-Closing Metathesis of Ene-Dienes. Competitive Intramolecular Regioselection as a Function of Chain Length

ChemInform Abstract: Solution to the C3—Arylation of Indazoles: Development of a Scalable Method

Systematic Analysis of the Intramolecular Competition Associated with the Ring Closing Metathesis of Ene-Diene Systems of Differing Chain Length with a Pair of Ruthenium Catalysts

ChemInform Abstract: Total Synthesis of (-)-Okilactomycin

Mono- and Bis-Acrolein Derivatives by Reliable and Efficient One-Step Methylenation of Aldehyde Precursors

ChemInform Abstract: Total Syntheses of the Assigned Structures of Lituarines B and C

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