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A 2-oxa-spiro[5.4]decane scaffold displays neurotrophic, neurogenic and anti-neuroinflammatory activities with high potential for development as a versatile CNS therapeutic

Scientific reports, 2017-05, Vol.7 (1), p.1492-13, Article 1492

2017

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PHLPP1 promotes neutral lipid accumulation through AMPK/ChREBP-dependent lipid uptake and fatty acid synthesis pathways

iScience, 2022-02, Vol.25 (2), p.103766-103766, Article 103766

2022

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Versatile Route to Benzoannulated Medium-Ring Carbocycles via Aryne Insertion into Cyclic 1,3-Diketones: Application to a Synthesis of Radermachol

Organic letters, 2016-06, Vol.18 (12), p.2832-2835

2016

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A General Carbazole Synthesis via Stitching of Indole–Ynones with Nitromethanes: Application to Total Synthesis of Carbazomycin A, Calothrixin B, and Staurosporinone

Organic letters, 2019-05, Vol.21 (9), p.3372-3376

2019

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Nitromethane as a Carbanion Source for Domino Benzoannulation with Ynones: One‐Pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine

Angewandte Chemie International Edition, 2018-12, Vol.57 (51), p.16847-16851

International ed. in English, 2018

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Spiroannulation of Oxindoles via Aryne and Alkyne Incorporation: Substituent-Diverted, Transition-Metal-Free, One-Pot Access to Spirooxindoles

Organic letters, 2017-06, Vol.19 (12), p.3119-3122

2017

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Stitching Oxindoles and Ynones in a Domino Process: Access to Spirooxindoles and Application to a Short Synthesis of Spindomycin B

Organic letters, 2017-11, Vol.19 (22), p.6152-6155

2017

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From vinyl pyranoses to carbasugars by an iron-catalyzed reaction complementary to classical Ferrier carbocyclization

Chemical communications (Cambridge, England), 2009-01 (31), p.4717-4719

2009

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Benzannulation of arynes with dimethylacetonedicarboxylates via an insertion-fragmentation-Dieckman-aromatization cascade: Expeditious entry to naphthoresorcinols and binaphthoresorcinols

Tetrahedron, 2019-05, Vol.75 (21), p.2923-2932

2019

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Multiple Aryne Insertions into Oxindoles: Synthesis of Bioactive 3,3-Diarylated Oxindoles and Dibenzo[b,e]azepin-6-ones

Organic letters, 2016-12, Vol.18 (23), p.6184-6187

2016

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Grignard Reagents as Niche Bases in the Synthesis of Pharmaceutically Relevant Molecules

ChemistrySelect (Weinheim), 2022-02, Vol.7 (5), p.n/a

2022

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An enantiodivergent formal synthesis of paecilomycine A

Tetrahedron letters, 2012-02, Vol.53 (7), p.829-832

2012

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Model studies towards paecilomycine A-C: exploring scaffold diversity through a key intramolecular Pauson-Khand reaction

Tetrahedron letters, 2011-04, Vol.52 (14), p.1663-1666

2011

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A novel natural product inspired scaffold with robust neurotrophic, neurogenic and neuroprotective action

Scientific reports, 2015-09, Vol.5 (1), p.14134-14134, Article 14134

2015

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Diverted organic synthesis (DOS): accessing a new, natural product inspired, neurotrophically active scaffold through an intramolecular Pauson-Khand reaction

Organic & biomolecular chemistry, 2012-09, Vol.10 (34), p.6830-6833

2012

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Nitromethane as a Carbanion Source for Domino Benzoannulation with Ynones: One‐Pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine

Angewandte Chemie, 2018-12, Vol.130 (51), p.17089-17093

2018

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Total synthesis of gabosines via an iron-catalyzed intramolecular tandem aldol process

Tetrahedron, 2011-12, Vol.67 (48), p.9305-9310

2011

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Diverted organic synthesis (DOS): accessing a new, natural product inspired, neurotrophically active scaffold through an intramolecular Pauson-Khand reactionElectronic supplementary Information (ESI) available: Experimental details and 1H, 13C spectra available here. CCDC 876473. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob26107c

2012-08

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Model studies towards paecilomycine A―C: exploring scaffold diversity through a key intramolecular Pauson―Khand reaction

Tetrahedron letters, , Vol.52 (14), p.1663-1666

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ChemInform Abstract: Versatile Route to Benzoannulated Medium‐Ring Carbocycles via Aryne Insertion into Cyclic 1,3‐Diketones: Application to a Synthesis of Radermachol

ChemInform, 2016-10, Vol.47 (44), p.no-no

2016

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ChemInform Abstract: From Vinyl Pyranoses to Carbasugars by an Iron-Catalyzed Reaction Complementary to Classical Ferrier Carbocyclization

ChemInform, 2009-12, Vol.40 (52), p.no-no

2009

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Measuring the Impact of Microfinance on Economic Enhancement of Women: Analysis with Special Reference to India

Global business review, 2023-10, Vol.24 (5), p.1076-1091

2023

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Expiration-Day Effects on Index Futures: Evidence from Indian Market

The Journal of Asian Finance, 2020, Economics and Business , 7(11), 35, pp.95-100

2020

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Expiration-Day Effects on Index Futures: Evidence from Indian Market

The Journal of Asian finance, economics, and business, 2020-11, Vol.7 (11), p.95-100

2020

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A 2-oxa-spiro[5.4]decane scaffold displays neurotrophic, neurogenic and anti-neuroinflammatory activities with high potential for development as a versatile CNS therapeutic

PHLPP1 promotes neutral lipid accumulation through AMPK/ChREBP-dependent lipid uptake and fatty acid synthesis pathways

Versatile Route to Benzoannulated Medium-Ring Carbocycles via Aryne Insertion into Cyclic 1,3-Diketones: Application to a Synthesis of Radermachol

A General Carbazole Synthesis via Stitching of Indole–Ynones with Nitromethanes: Application to Total Synthesis of Carbazomycin A, Calothrixin B, and Staurosporinone

Nitromethane as a Carbanion Source for Domino Benzoannulation with Ynones: One‐Pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine

Spiroannulation of Oxindoles via Aryne and Alkyne Incorporation: Substituent-Diverted, Transition-Metal-Free, One-Pot Access to Spirooxindoles

Stitching Oxindoles and Ynones in a Domino Process: Access to Spirooxindoles and Application to a Short Synthesis of Spindomycin B

From vinyl pyranoses to carbasugars by an iron-catalyzed reaction complementary to classical Ferrier carbocyclization

Benzannulation of arynes with dimethylacetonedicarboxylates via an insertion-fragmentation-Dieckman-aromatization cascade: Expeditious entry to naphthoresorcinols and binaphthoresorcinols

Multiple Aryne Insertions into Oxindoles: Synthesis of Bioactive 3,3-Diarylated Oxindoles and Dibenzo[b,e]azepin-6-ones

Grignard Reagents as Niche Bases in the Synthesis of Pharmaceutically Relevant Molecules

An enantiodivergent formal synthesis of paecilomycine A

Model studies towards paecilomycine A-C: exploring scaffold diversity through a key intramolecular Pauson-Khand reaction

A novel natural product inspired scaffold with robust neurotrophic, neurogenic and neuroprotective action

Diverted organic synthesis (DOS): accessing a new, natural product inspired, neurotrophically active scaffold through an intramolecular Pauson-Khand reaction

Nitromethane as a Carbanion Source for Domino Benzoannulation with Ynones: One‐Pot Synthesis of Polyfunctional Naphthalenes and a Total Synthesis of Macarpine

Total synthesis of gabosines via an iron-catalyzed intramolecular tandem aldol process

Model studies towards paecilomycine A―C: exploring scaffold diversity through a key intramolecular Pauson―Khand reaction

ChemInform Abstract: Versatile Route to Benzoannulated Medium‐Ring Carbocycles via Aryne Insertion into Cyclic 1,3‐Diketones: Application to a Synthesis of Radermachol

ChemInform Abstract: From Vinyl Pyranoses to Carbasugars by an Iron-Catalyzed Reaction Complementary to Classical Ferrier Carbocyclization

Measuring the Impact of Microfinance on Economic Enhancement of Women: Analysis with Special Reference to India

Expiration-Day Effects on Index Futures: Evidence from Indian Market

Expiration-Day Effects on Index Futures: Evidence from Indian Market

Translational Chickpea Genomics Consortium to Accelerate Genetic Gains in Chickpea ( Cicer arietinum L.)

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