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Asymmetric Synthetic Strategies of (R)-(–)-Baclofen: An Antispastic Drug

Synthesis (Stuttgart), 2018-01, Vol.50 (2), p.211-226

2018

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A three-step total synthesis of goniothalesdiol A using a one-pot Sharpless epoxidation/regioselective epoxide ring-opening

Tetrahedron letters, 2017-03, Vol.58 (11), p.1037-1039

2017

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Biosynthesis-Inspired Total Synthesis of Bioactive Styryllactones (+)-Goniodiol, (6S,7S,8S)‑Goniodiol, (−)-Parvistone D, and (+)-Parvistone E

Journal of natural products (Washington, D.C.), 2016-08, Vol.79 (8), p.2060-2065

2016

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A simple removable aliphatic nitrile template 2-cyano-2,2-di-isobutyl acetic acid for remote meta -selective C–H functionalization

Organic Chemistry Frontiers, 2021-05, Vol.8 (9), p.1959-1969

2021

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Development of a triazolobenzodiazepine-based PET probe for subtype-selective vasopressin 1A receptor imaging

Pharmacological research, 2021-11, Vol.173, p.105886-105886, Article 105886

2021

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Stereoselective total synthesis of sphingolipids

Journal of chemical sciences (Bangalore, India), 2016-11, Vol.128 (11), p.1789-1794

2016

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Ammonium Nitrate: A Biodegradable and Efficient Catalyst for the Direct Amidation of Esters under Solvent-free Conditions

Chemistry letters, 2015, Vol.44 (2), p.138-140

2015

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Palladium-Catalyzed Aerobic Oxidative Coupling of ortho-(Alkynyl)styrenes with Allylic Alcohols via 6-endo-dig Cyclization: Regioselective Construction of Polysubstituted Naphthalenes

Journal of organic chemistry, 2019-10, Vol.84 (20), p.12856-12870

2019

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Protecting-Group-Free Total Synthesis of 8-Methoxygoniodiol

Synthesis (Stuttgart), 2016-12, Vol.48 (23), p.4300-4304

Ramesh, Perla

2016

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Design, Synthesis, and Cytotoxic Evaluation of Etodolac-1,3,4-oxadiazole-1,2,3-triazole Molecules

SynOpen (2017), 2018-01, Vol.2 (1), p.0017-0024

2018

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A Five‐Step Total Synthesis of Parvistone B

ChemistrySelect (Weinheim), 2016-08, Vol.1 (12), p.3244-3246

Ramesh, Perla

2016

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First total synthesis of the proposed structure of cryptorigidifoliol B

Tetrahedron letters, 2016-05, Vol.57 (19), p.2100-2102

2016

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Recyclable Aliphatic Nitrile-Template Enabled Remote meta-C–H Functionalization at Room Temperature

Journal of organic chemistry, 2022-03, Vol.87 (5), p.2204-2221

2022

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Total synthesis of cryptomoscatone F1 through an asymmetric aldol approach

Tetrahedron: asymmetry, 2015-12, Vol.26 (21-22), p.1251-1255

2015

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Knoevenagel condensation of diethylmalonate with aldehydes catalyzed by immobilized bovine serum albumin (BSA)

RSC advances, 2014, Vol.4 (15), p.7368

2014

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Stereoselective total synthesis of cryptomoscatone D1 and (5R,7S)-kurzilactone via ring closing metathesis

Tetrahedron letters, 2016-03, Vol.57 (10), p.1087-1089

2016

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Copper-catalyzed aerobic oxidative intramolecular amidation of 2-aminophenylacetylenes: a domino process for the synthesis of isatinPart 241 in the series, "Studies on novel synthetic methodologies".Electronic supplementary information (ESI) available: Experimental procedures and spectral data of the products. See DOI: 10.1039/c7nj02441j

2017-11

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Efficient Resolution of cis-(±)-Dimethyl 1‑Acetylpiperidine-2,3-dicarboxylate with Soluble Candida antarctica Lipase B (CAL B)

Organic process research & development, 2015-01, Vol.19 (1), p.296-301

2015

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An Efficient Stereoselective Total Synthesis of Bioactive (3R,5R)-1-(4-Hydroxyphenyl)-7-phenylheptane-3,5-diol via Asymmetric Aldol Reaction

Helvetica chimica acta, 2016-01, Vol.99 (1), p.70-72

2016

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First total synthesis of the highly potent antitumor lactones 8-chlorogoniodiol and parvistone A: Exploiting a bioinspired late-stage epoxide ring-opening

Tetrahedron: asymmetry, 2017-02, Vol.28 (2), p.246-249

2017

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Copper-catalyzed aerobic oxidative intramolecular amidation of 2-aminophenylacetylenes: a domino process for the synthesis of isatin

New journal of chemistry, 2017, Vol.41 (22), p.13754-13759

2017

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An efficient catalyst-free one-pot synthesis of primary amides from the aldehydes of the Baylis–Hillman reaction

New journal of chemistry, 2017, Vol.41 (17), p.9203-9209

2017

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Design and synthesis of 1,2,3-triazole–etodolac hybrids as potent anticancer molecules

RSC advances, 2017-01, Vol.7 (38), p.23680-23686

2017

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An efficient catalyst-free one-pot synthesis of primary amides from the aldehydes of the Baylis-Hillman reactionElectronic supplementary information (ESI) available. CCDC 1495303. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7nj01965c

2017-08

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Stereoselective total synthesis of pectinolide H and 4'-epi-pectinolide H

European journal of chemistry, 2015-03, Vol.6 (1), p.93-97

2015

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Asymmetric Synthetic Strategies of (R)-(–)-Baclofen: An Antispastic Drug

A three-step total synthesis of goniothalesdiol A using a one-pot Sharpless epoxidation/regioselective epoxide ring-opening

Biosynthesis-Inspired Total Synthesis of Bioactive Styryllactones (+)-Goniodiol, (6S,7S,8S)‑Goniodiol, (−)-Parvistone D, and (+)-Parvistone E

A simple removable aliphatic nitrile template 2-cyano-2,2-di-isobutyl acetic acid for remote meta -selective C–H functionalization

Development of a triazolobenzodiazepine-based PET probe for subtype-selective vasopressin 1A receptor imaging

Stereoselective total synthesis of sphingolipids

Ammonium Nitrate: A Biodegradable and Efficient Catalyst for the Direct Amidation of Esters under Solvent-free Conditions

Palladium-Catalyzed Aerobic Oxidative Coupling of ortho-(Alkynyl)styrenes with Allylic Alcohols via 6-endo-dig Cyclization: Regioselective Construction of Polysubstituted Naphthalenes

Protecting-Group-Free Total Synthesis of 8-Methoxygoniodiol

Design, Synthesis, and Cytotoxic Evaluation of Etodolac-1,3,4-oxadiazole-1,2,3-triazole Molecules

A Five‐Step Total Synthesis of Parvistone B

First total synthesis of the proposed structure of cryptorigidifoliol B

Recyclable Aliphatic Nitrile-Template Enabled Remote meta-C–H Functionalization at Room Temperature

Total synthesis of cryptomoscatone F1 through an asymmetric aldol approach

Knoevenagel condensation of diethylmalonate with aldehydes catalyzed by immobilized bovine serum albumin (BSA)

Stereoselective total synthesis of cryptomoscatone D1 and (5R,7S)-kurzilactone via ring closing metathesis

Efficient Resolution of cis-(±)-Dimethyl 1‑Acetylpiperidine-2,3-dicarboxylate with Soluble Candida antarctica Lipase B (CAL B)

An Efficient Stereoselective Total Synthesis of Bioactive (3R,5R)-1-(4-Hydroxyphenyl)-7-phenylheptane-3,5-diol via Asymmetric Aldol Reaction

First total synthesis of the highly potent antitumor lactones 8-chlorogoniodiol and parvistone A: Exploiting a bioinspired late-stage epoxide ring-opening

Copper-catalyzed aerobic oxidative intramolecular amidation of 2-aminophenylacetylenes: a domino process for the synthesis of isatin

An efficient catalyst-free one-pot synthesis of primary amides from the aldehydes of the Baylis–Hillman reaction

Design and synthesis of 1,2,3-triazole–etodolac hybrids as potent anticancer molecules

An efficient catalyst-free one-pot synthesis of primary amides from the aldehydes of the Baylis-Hillman reactionElectronic supplementary information (ESI) available. CCDC 1495303. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7nj01965c

Stereoselective total synthesis of pectinolide H and 4'-epi-pectinolide H

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