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Facile synthesis and cytotoxicity of substituted uracil-1'(N)-acetic acid and 4-pyridone-1'(N)-acetic acid esters of 20(S)-camptothecins

Journal of asian natural products research, 2024-02, Vol.26 (2), p.259-268

2024

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Synthesis and antiviral activity of lycorine derivatives

Journal of asian natural products research, 2020-12, Vol.22 (12), p.1188-1196

2020

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LiCl-promoted amination of β-methoxy amides (γ-lactones)

RSC advances, 2020-09, Vol.1 (57), p.34938-34942

2020

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Practical Ligand-Free Copper-Catalysed Short-Chain Alkoxylation of Unactivated Aryl Bromides

European journal of organic chemistry, 2015-07, Vol.2015 (21), p.4744-4755

2015

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The antitumor activity and mechanism of MCL3 in G422 glioblastoma

World Journal of Traditional Chinese Medicine, 2020-07, Vol.6 (3), p.353

2020

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Blocking the major inflammatory pathways by newly synthesized thiadiazine derivatives via in-vivo, in-vitro and in-silico mechanism

Bioorganic chemistry, 2023-11, Vol.140, p.106760-106760, Article 106760

2023

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Design, synthesis and biological evaluation of aloperine derivatives as potential anticancer agents

Journal of asian natural products research, 2024-09, Vol.26 (9), p.1057-1086

2024

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A highly efficient approach to vanillin starting from 4-cresol

Green chemistry : an international journal and green chemistry resource : GC, 2014-01, Vol.16 (5), p.2807-2814

2014

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Synthesis and antitumor activity of novel substituted uracil-1′(N)-acetic acid ester derivatives of 20(S)-camptothecins

European journal of medicinal chemistry, 2017-01, Vol.125, p.1235-1246

2017

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Synthesis and Antiviral Activity of Phthiobuzone Analogues

Chemical and Pharmaceutical Bulletin, 2010/02/01, Vol.58(2), pp.208-211

2010

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Synthesis and cytotoxic activity of heterocycle-substituted phthalimide derivatives

Chinese chemical letters, 2010-08, Vol.21 (8), p.902-904

2010

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Synthesis and antitumor activity of 20- O-linked nitrogen-based camptothecin ester derivatives

Bioorganic & medicinal chemistry, 2004-07, Vol.12 (13), p.3657-3662

2004

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An Efficient Strategy for Protecting Dihydroxyl Groups of Catechols

Synlett, 2013-04, Vol.24 (6), p.741-746

2013

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Synthesis and Antiviral Activity of Phthiobuzone Analogues

Chemical & Pharmaceutical Bulletin, 2010, Vol.58 (2), p.208-212

2010

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Synthesis and cytotoxicity of novel 20-O-linked homocamptothecin ester derivatives as potent topoisomerase I inhibitors

Journal of asian natural products research, 2013-11, Vol.15 (11), p.1179-1188

2013

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Synthesis and antitumor activity of heterocyclic acid ester derivatives of 20S-camptothecins

Chinese chemical letters, 2007-11, Vol.18 (11), p.1335-1338

2007

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Regioselective synthesis and cytotoxicities of camptothecin derivatives modified at the 7-, 10- and 20-positions

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (21), p.3739-3741

2003

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Facile synthesis and cytotoxicity of 5- C-alkylates of 20( S)-camptothecins

Chinese chemical letters, 2008-10, Vol.19 (10), p.1202-1205

2008

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A Solid-Phase Approach to Fluorobenzimidazoles and Fluoro-2-hydroxyquinoxalines Using ’One-Bead-Two-Compound’ Method

Synlett, 2004-07, Vol.2004 (9), p.1607-1609

2004

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Current status of camptothecin derivatives as natural antitumor agents

Yao hsüeh hsüeh pao, 2003-09, Vol.38 (9), p.715

2003

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Synthesis and antitumor activity of nitrogen-based thiocolchicine derivatives

Yao hsüeh hsüeh pao, 2006-11, Vol.41 (11), p.1057

2006

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Recent progress in structure-activity relationship studies on the anticancer drug colchicine and its analogues

Yao hsüeh hsüeh pao, 2002-10, Vol.37 (10), p.821

2002

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Synthesis and antitumor activity of 20-O-linked camptothecin ester derivatives

Yao hsüeh hsüeh pao, 2004-08, Vol.39 (8), p.591

2004

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Synthesis and antitumor activity of A-ring modified hexacyclic analogues of camptothecin

Yao hsüeh hsüeh pao, 2005-03, Vol.40 (3), p.241

2005

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A highly efficient approach to vanillin starting from 4-cresolElectronic supplementary information (ESI) available. See DOI: 10.1039/c4gc00003j

2014-04

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Facile synthesis and cytotoxicity of substituted uracil-1'(N)-acetic acid and 4-pyridone-1'(N)-acetic acid esters of 20(S)-camptothecins

Synthesis and antiviral activity of lycorine derivatives

LiCl-promoted amination of β-methoxy amides (γ-lactones)

Practical Ligand-Free Copper-Catalysed Short-Chain Alkoxylation of Unactivated Aryl Bromides

The antitumor activity and mechanism of MCL3 in G422 glioblastoma

Blocking the major inflammatory pathways by newly synthesized thiadiazine derivatives via in-vivo, in-vitro and in-silico mechanism

Design, synthesis and biological evaluation of aloperine derivatives as potential anticancer agents

A highly efficient approach to vanillin starting from 4-cresol

Synthesis and antitumor activity of novel substituted uracil-1′(N)-acetic acid ester derivatives of 20(S)-camptothecins

Synthesis and Antiviral Activity of Phthiobuzone Analogues

Synthesis and cytotoxic activity of heterocycle-substituted phthalimide derivatives

Synthesis and antitumor activity of 20- O-linked nitrogen-based camptothecin ester derivatives

An Efficient Strategy for Protecting Dihydroxyl Groups of Catechols

Synthesis and Antiviral Activity of Phthiobuzone Analogues

Synthesis and cytotoxicity of novel 20-O-linked homocamptothecin ester derivatives as potent topoisomerase I inhibitors

Synthesis and antitumor activity of heterocyclic acid ester derivatives of 20S-camptothecins

Regioselective synthesis and cytotoxicities of camptothecin derivatives modified at the 7-, 10- and 20-positions

Facile synthesis and cytotoxicity of 5- C-alkylates of 20( S)-camptothecins

A Solid-Phase Approach to Fluorobenzimidazoles and Fluoro-2-hydroxyquinoxalines Using ’One-Bead-Two-Compound’ Method

Current status of camptothecin derivatives as natural antitumor agents

Synthesis and antitumor activity of nitrogen-based thiocolchicine derivatives

Recent progress in structure-activity relationship studies on the anticancer drug colchicine and its analogues

Synthesis and antitumor activity of 20-O-linked camptothecin ester derivatives

Synthesis and antitumor activity of A-ring modified hexacyclic analogues of camptothecin

A highly efficient approach to vanillin starting from 4-cresolElectronic supplementary information (ESI) available. See DOI: 10.1039/c4gc00003j

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