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Divergent synthesis of nitrogen heterocycles via H2O-mediated hydride transfer reactions

Green chemistry : an international journal and green chemistry resource : GC, 2023-07, Vol.25 (13), p.5134-5141

2023

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Organocatalytic Michael/Michael Cycloaddition Enabled Asymmetric Construction of Hexahydroxanthones with Skeletal Diversity

Advanced synthesis & catalysis, 2019-06, Vol.361 (12), p.2836-2843

2019

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Highly Efficient and Stereocontrolled Construction of 3,3′-Pyrrolidonyl Spirooxindoles via Organocatalytic Domino Michael/Cyclization Reaction

Organic letters, 2013-03, Vol.15 (6), p.1246-1249

2013

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Stereocontrolled construction of six vicinal stereogenic centers on a hexahydroxanthone framework through a formal [2+1+3] annulation

Chemical communications (Cambridge, England), 2019, Vol.55 (93), p.143-146

2019

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Study on antitumor activities of the chrysin-chromene-spirooxindole on Lewis lung carcinoma C57BL/6 mice in vivo

Bioorganic & medicinal chemistry letters, 2020-09, Vol.30 (17), p.127410-127410, Article 127410

2020

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Dienolate‐Mediated, Regioselective C2‐Polarity Reversal of Chromone‐Based Reactants and Their Application in Nucleophilic Strategies

Advanced synthesis & catalysis, 2020-12, Vol.362 (23), p.5352-5357

2020

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Oxindole‐chromones C3 Synthons Directed Stereocontrolled Construction of Five Contiguous Stereocenters on Spiro[tetrahydrocyclopenta[b]chromanone‐oxindole]s

Advanced synthesis & catalysis, 2019-12, Vol.361 (23), p.5328-5333

2019

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Synthesis and antitumor activities of 4-(1H-indol-1-yl)-4-oxobutanoic acid spliced podophyllotoxin derivatives

Synthetic communications, 2023-02, Vol.53 (3), p.262-273

2023

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Ammonium hydroxide as the ultimate amino source for the synthesis of N -unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination

Green chemistry : an international journal and green chemistry resource : GC, 2020-03, Vol.22 (6), p.1837-1841

2020

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Fischer's base-triggered formal (3+2) cycloadditions with 3-isothiocyanato oxindoles as acceptor-donor synthons

Chemical communications (Cambridge, England), 2023-04, Vol.59 (31), p.4652-4655

2023

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Design, synthesis and evaluation of structurally diverse ortho -acylphenol-diindolylmethane hybrids as anticancer agents

New journal of chemistry, 2022-01, Vol.46 (3), p.1295-1307

2022

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Design and Synthesis of Rigid‐Featured Tertiary Amine‐Derived C2‐Symmetric Chiral Furan‐N,N′‐dioxide Ligands

European journal of organic chemistry, 2023-11, Vol.26 (42)

2023

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Regio- and stereoselective synthesis and evaluation of densely functionalized bispiro[oxindole-isoxazole-indandione] hybrids as anticancer agents

New journal of chemistry, 2022-10, Vol.46 (4), p.19442-19454

2022

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Diastereoselective construction of a library of structural bispiro[butyrolactone/valerolactone–pyrrolidine–indanedione] hybrids via 1,3-dipolar cycloaddition reactions

New journal of chemistry, 2022-06, Vol.46 (25), p.11975-11979

2022

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Py-2NO ligand enabled Ni()-catalyzed asymmetric Michael addition reaction of indoles with β,γ-unsaturated α-keto esters

New journal of chemistry, 2024-01, Vol.48 (4), p.1688-1695

2024

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Trimethylindolenines as C-N synthons for the assembly of spiro[oxindole-thioxoimidazolidine-indoline] hybrids in formal [3+2] cycloadditions

New journal of chemistry, 2023-07, Vol.47 (26), p.12296-1233

2023

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Advances in chromone-based reactants in the ring opening and skeletal reconstruction reaction: access to skeletally diverse salicyloylbenzene/heterocycle derivatives

Organic & biomolecular chemistry, 2022-06, Vol.2 (23), p.4681-4698

2022

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Clinical Significance of Different Profiles of anti-Ro Antibodies in Connective Tissue Diseases

Journal of Immunology Research, 2023-01, Vol.2023, p.9195157-11

2023

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Phen-2NO, a new C2-symmetric rigid-featured tetradentate ligand, and its application in the asymmetric alkylation reaction of indoles

New journal of chemistry, 2024-04, Vol.48 (15), p.6670-6675

2024

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Design, synthesis and evaluation of structurally diverse polycyclic harmaline scaffolds as anticancer agents

New journal of chemistry, 2024-04, Vol.48 (14), p.6322-6334

2024

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Catalytic asymmetric Michael/cyclization reaction of 3-isothiocyanato thiobutyrolactone: an approach to the construction of a library of bispiro[pyrazolone-thiobutyrolactone] skeletons

Organic & biomolecular chemistry, 2022-06, Vol.2 (25), p.56-565

2022

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Design, synthesis and evaluation of multi-pharmacophore-containing spiropolycyclic harmaline-based hybrids as anticancer agents

New journal of chemistry, 2023-03, Vol.47 (13), p.673-685

2023

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Ring opening and skeletal reconstruction of 3-vinyl benzofuranone-chromone synthons: catalyst-free access to skeletally-diverse 2-pyridone and optically active imidazoline derivatives

Organic & biomolecular chemistry, 2022-03, Vol.2 (11), p.2227-2232

2022

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Thermal-mediated [1,3]-hydrogen transfer as the key step: access to oxindole-chromone hybrid collection with structural diversity

Organic & biomolecular chemistry, 2019-11, Vol.17 (44), p.9567-9572

2019

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An asymmetric iminium ion catalysis-enabled cascade cycloaddition reaction of chromone-oxindole synthons with enals: construction of a spirooxindole-hexahydroxanthone framework

Organic & biomolecular chemistry, 2019-09, Vol.17 (36), p.8369-8373

2019

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Divergent synthesis of nitrogen heterocycles via H2O-mediated hydride transfer reactions

Organocatalytic Michael/Michael Cycloaddition Enabled Asymmetric Construction of Hexahydroxanthones with Skeletal Diversity

Highly Efficient and Stereocontrolled Construction of 3,3′-Pyrrolidonyl Spirooxindoles via Organocatalytic Domino Michael/Cyclization Reaction

Stereocontrolled construction of six vicinal stereogenic centers on a hexahydroxanthone framework through a formal [2+1+3] annulation

Study on antitumor activities of the chrysin-chromene-spirooxindole on Lewis lung carcinoma C57BL/6 mice in vivo

Dienolate‐Mediated, Regioselective C2‐Polarity Reversal of Chromone‐Based Reactants and Their Application in Nucleophilic Strategies

Oxindole‐chromones C3 Synthons Directed Stereocontrolled Construction of Five Contiguous Stereocenters on Spiro[tetrahydrocyclopenta[b]chromanone‐oxindole]s

Synthesis and antitumor activities of 4-(1H-indol-1-yl)-4-oxobutanoic acid spliced podophyllotoxin derivatives

Ammonium hydroxide as the ultimate amino source for the synthesis of N -unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination

Fischer's base-triggered formal (3+2) cycloadditions with 3-isothiocyanato oxindoles as acceptor-donor synthons

Design, synthesis and evaluation of structurally diverse ortho -acylphenol-diindolylmethane hybrids as anticancer agents

Design and Synthesis of Rigid‐Featured Tertiary Amine‐Derived C2‐Symmetric Chiral Furan‐N,N′‐dioxide Ligands

Regio- and stereoselective synthesis and evaluation of densely functionalized bispiro[oxindole-isoxazole-indandione] hybrids as anticancer agents

Diastereoselective construction of a library of structural bispiro[butyrolactone/valerolactone–pyrrolidine–indanedione] hybrids via 1,3-dipolar cycloaddition reactions

Py-2NO ligand enabled Ni()-catalyzed asymmetric Michael addition reaction of indoles with β,γ-unsaturated α-keto esters

Trimethylindolenines as C-N synthons for the assembly of spiro[oxindole-thioxoimidazolidine-indoline] hybrids in formal [3+2] cycloadditions

Advances in chromone-based reactants in the ring opening and skeletal reconstruction reaction: access to skeletally diverse salicyloylbenzene/heterocycle derivatives

Clinical Significance of Different Profiles of anti-Ro Antibodies in Connective Tissue Diseases

Phen-2NO, a new C2-symmetric rigid-featured tetradentate ligand, and its application in the asymmetric alkylation reaction of indoles

Design, synthesis and evaluation of structurally diverse polycyclic harmaline scaffolds as anticancer agents

Catalytic asymmetric Michael/cyclization reaction of 3-isothiocyanato thiobutyrolactone: an approach to the construction of a library of bispiro[pyrazolone-thiobutyrolactone] skeletons

Design, synthesis and evaluation of multi-pharmacophore-containing spiropolycyclic harmaline-based hybrids as anticancer agents

Ring opening and skeletal reconstruction of 3-vinyl benzofuranone-chromone synthons: catalyst-free access to skeletally-diverse 2-pyridone and optically active imidazoline derivatives

Thermal-mediated [1,3]-hydrogen transfer as the key step: access to oxindole-chromone hybrid collection with structural diversity

An asymmetric iminium ion catalysis-enabled cascade cycloaddition reaction of chromone-oxindole synthons with enals: construction of a spirooxindole-hexahydroxanthone framework

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