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Tandem Amination/Cycloisomerization of Aryl Propargylic Alcohols with 2-Aminopyridines as an Expedient Route to Imidazo[1,2-a]pyridines

European Journal of Organic Chemistry, 2011-12, Vol.2011 (36), p.7308-7316

2011

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Unexpected Enhancement of HDACs Inhibition by MeS Substitution at C-2 Position of Fluoro Largazole

Marine drugs, 2020-06, Vol.18 (7), p.344

2020

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Synthesis and Preliminary Biological Evaluation of Two Fluoroolefin Analogs of Largazole Inspired by the Structural Similarity of the Side Chain Unit in Psammaplin A

Marine drugs, 2019-06, Vol.17 (6), p.333

2019

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First Stereospecific Synthesis of (E)- or (Z)-α-Fluoroenones via a Kinetically Controlled Negishi Coupling Reaction

Journal of organic chemistry, 2006-05, Vol.71 (11), p.4316-4319

2006

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Synthesis of ∆3-2-hydroxybakuchiol analogues and their growth inhibitory activity against rat UMR106 cells

Molecules (Basel, Switzerland), 2014-02, Vol.19 (2), p.2213-2225

2014

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"One pot" synthesis of quinazolinone-[2,3]-fused polycyclic scaffolds in a three-step reaction sequence

Organic & biomolecular chemistry, 2024-06, Vol.22 (23), p.472-4726

2024

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Construction of indolizine scaffolds from α,ω-alkynoic acids and α,ω-vinylamines via sequential-relay catalysis in "one pot"

Organic & biomolecular chemistry, 2024-03, Vol.22 (12), p.2474-2479

2024

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Construction of indolizine scaffolds from α,ω-alkynoic acids and α,ω-vinylamines sequential-relay catalysis in "one pot"

Organic & biomolecular chemistry, 2024-03, Vol.22 (12), p.2474-2479

2024

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Discovery and synthesis of novel luteolin derivatives as DAT agonists

Bioorganic & medicinal chemistry, 2010-11, Vol.18 (22), p.7842-7848

2010

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Copper-catalyzed cross-coupling of amino acid-derived amides with (Z)-vinyl iodides: Unexpected solvent effect and preparation of plocabulin

Tetrahedron, 2021-03, Vol.83, p.131953, Article 131953

2021

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A Facile and Mild Method for the Synthesis of Terminal Bromofluoroolefins via Diethylzinc-Promoted Wittig Reaction

Organic letters, 2004-06, Vol.6 (13), p.2101-2104

2004

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Identification and immunological evaluation of novel TLR2 agonists through structural optimization of Diprovocim

European journal of medicinal chemistry, 2022-12, Vol.243, p.114771-114771, Article 114771

2022

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Synthesis and Evaluation of the Analogues of Penicillide against Cholesterol Ester Transfer Protein

Chinese journal of chemistry, 2013-03, Vol.31 (3), p.355-370

2013

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Ru-Catalyzed cascade reaction of α,ω-alkynoic acids and arylethylamines towards the synthesis of aryl-fused heterocycles

Organic chemistry frontiers an international journal of organic chemistry, 2020-02, Vol.7 (4), p.660-665

2020

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A Novel Diastereoselective Synthesis of (Z)-Fluoroalkenes via a Nozaki−Hiyama−Kishi-Type Reaction

Journal of organic chemistry, 2005-03, Vol.70 (5), p.1911-1914

2005

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Regio-selective chlorination of vinca alkaloids catalyzed by Lewis acid

Science China. Chemistry, 2011-07, Vol.54 (7), p.1039-1043

2011

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Synthesis of the analogs of plocabulin and their preliminary structure-activity relationship study

Bioorganic & medicinal chemistry letters, 2021-11, Vol.51, p.128355-128355, Article 128355

2021

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Cs2CO3-promoted defluorination and functionalization of α-CF3 carbonyl compounds in the presence of N-, O-, and/or S-nucleophiles

RSC advances, 2018-01, Vol.8 (29), p.16019-16023

2018

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A fluorine scan on the Zn2+-binding thiolate side chain of HDAC inhibitor largazole: Synthesis, biological evaluation, and molecular modeling

European journal of medicinal chemistry, 2019-11, Vol.182, p.111672-111672, Article 111672

2019

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Synthesis, biological evaluation, and molecular modeling of ORM-10921 and its analogs as α 2C -adrenoceptor antagonists

Archiv der Pharmazie (Weinheim), 2023-08, Vol.356 (8), p.e2300125

2023

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Synthesis, biological evaluation, and molecular modeling of ORM‐10921 and its analogs as α2C‐adrenoceptor antagonists

Archiv der Pharmazie (Weinheim), 2023-08, Vol.356 (8), p.e2300125-n/a

2023

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Corrigendum to “A fluorine scan on the Zn2+-binding thiolate side chain of HDAC inhibitor largazole: Synthesis, biological evaluation, and molecular modeling” [Eur. J. Med. Chem. 182 (2019) 111672]

European journal of medicinal chemistry, 2020-07, Vol.198, p.112340-112340, Article 112340

2020

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Synthesis of imidazo[1,2 a]pyridines via three-component reaction of 2-aminopyridines, aldehydes and alkynes

Tetrahedron letters, 2010-09, Vol.51 (35), p.4605-4608

2010

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Synthesis of the molecular hybrid inspired by Largazole and Psammaplin A

Tetrahedron, 2018-02, Vol.74 (5), p.549-555

2018

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Discovery, synthesis, biological evaluation and molecular docking study of (R)-5-methylmellein and its analogs as selective monoamine oxidase A inhibitors

Bioorganic & medicinal chemistry, 2019-05, Vol.27 (10), p.2027-2040

2019

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Tandem Amination/Cycloisomerization of Aryl Propargylic Alcohols with 2-Aminopyridines as an Expedient Route to Imidazo[1,2-a]pyridines

Unexpected Enhancement of HDACs Inhibition by MeS Substitution at C-2 Position of Fluoro Largazole

Synthesis and Preliminary Biological Evaluation of Two Fluoroolefin Analogs of Largazole Inspired by the Structural Similarity of the Side Chain Unit in Psammaplin A

First Stereospecific Synthesis of (E)- or (Z)-α-Fluoroenones via a Kinetically Controlled Negishi Coupling Reaction

Synthesis of ∆3-2-hydroxybakuchiol analogues and their growth inhibitory activity against rat UMR106 cells

"One pot" synthesis of quinazolinone-[2,3]-fused polycyclic scaffolds in a three-step reaction sequence

Construction of indolizine scaffolds from α,ω-alkynoic acids and α,ω-vinylamines via sequential-relay catalysis in "one pot"

Construction of indolizine scaffolds from α,ω-alkynoic acids and α,ω-vinylamines sequential-relay catalysis in "one pot"

Discovery and synthesis of novel luteolin derivatives as DAT agonists

Copper-catalyzed cross-coupling of amino acid-derived amides with (Z)-vinyl iodides: Unexpected solvent effect and preparation of plocabulin

A Facile and Mild Method for the Synthesis of Terminal Bromofluoroolefins via Diethylzinc-Promoted Wittig Reaction

Identification and immunological evaluation of novel TLR2 agonists through structural optimization of Diprovocim

Synthesis and Evaluation of the Analogues of Penicillide against Cholesterol Ester Transfer Protein

Ru-Catalyzed cascade reaction of α,ω-alkynoic acids and arylethylamines towards the synthesis of aryl-fused heterocycles

A Novel Diastereoselective Synthesis of (Z)-Fluoroalkenes via a Nozaki−Hiyama−Kishi-Type Reaction

Regio-selective chlorination of vinca alkaloids catalyzed by Lewis acid

Synthesis of the analogs of plocabulin and their preliminary structure-activity relationship study

Cs2CO3-promoted defluorination and functionalization of α-CF3 carbonyl compounds in the presence of N-, O-, and/or S-nucleophiles

A fluorine scan on the Zn2+-binding thiolate side chain of HDAC inhibitor largazole: Synthesis, biological evaluation, and molecular modeling

Synthesis, biological evaluation, and molecular modeling of ORM-10921 and its analogs as α 2C -adrenoceptor antagonists

Synthesis, biological evaluation, and molecular modeling of ORM‐10921 and its analogs as α2C‐adrenoceptor antagonists

Corrigendum to “A fluorine scan on the Zn2+-binding thiolate side chain of HDAC inhibitor largazole: Synthesis, biological evaluation, and molecular modeling” [Eur. J. Med. Chem. 182 (2019) 111672]

Synthesis of imidazo[1,2 a]pyridines via three-component reaction of 2-aminopyridines, aldehydes and alkynes

Synthesis of the molecular hybrid inspired by Largazole and Psammaplin A

Discovery, synthesis, biological evaluation and molecular docking study of (R)-5-methylmellein and its analogs as selective monoamine oxidase A inhibitors

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