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Cucurbit[7]uril: Synthesis and quenching the quorum sensing in bacteria

Journal of molecular structure, 2022-01, Vol.1248, p.131505, Article 131505

2022

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Functionalization of Cyclodextrins via Reactions of 2,3-Anhydrocyclodextrins

Journal of organic chemistry, 2003-11, Vol.68 (24), p.9456-9466

2003

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Three‐in‐One: Miniature Models of Natural Acyl‐Transfer Systems Enable Vector‐Selective Reaction on the Primary Side of Cyclodextrins

Chemistry : a European journal, 2022-02, Vol.28 (8), p.e202103940-n/a

2022

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A one-pot synthetic method for the hetero-bifunctionalization of α-cyclodextrin at the secondary hydroxyl side with high clockwise-counterclockwise selectivity

Organic & biomolecular chemistry, 2017-05, Vol.15 (19), p.477-48

2017

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Restriction of guest rotation based on the distortion of a cyclodextrin cavity

Chemical communications (Cambridge, England), 2000-01 (7), p.541-542

2000

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Synthesis and binding behaviors of monomethyl cucurbit[6]uril

Tetrahedron letters, 2011-09, Vol.52 (36), p.4646-4649

2011

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Imidazolyl Cyclodextrins: Artificial Serine Proteases Enabling Regiospecific Reactions

Angewandte Chemie International Edition, 2007-01, Vol.46 (26), p.5024-5027

2007

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Heptakis(6-deoxy-6-guanidino)-β-cyclodextrin: an artificial model for mitochondrial ADP/ATP carrier

Tetrahedron letters, 2007-05, Vol.48 (19), p.3479-3483

2007

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A Vector-Selective Reaction Enables Efficient Construction of Specific Topology upon the Primary Side of β-Cyclodextrin

Organic letters, 2007-10, Vol.9 (22), p.4591-4594

2007

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The first topologically controlled synthesis of doubly bridged beta-cyclodextrin dimers

Chemical communications (Cambridge, England), 2007-01 (8), p.828-830

2007

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Selective modification of beta-cyclodextrin: an unexpected tandem reaction enables the cross-linking of C2(A) and C2(B) via a sulfur atom

Chemical communications (Cambridge, England), 2007-08 (30), p.3157-3159

2007

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A facile sulfonylation method enabling direct syntheses of per(2- O-sulfonyl)-β-cyclodextrins

Tetrahedron letters, 2006-12, Vol.47 (50), p.8837-8840

2006

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Hetero-bifunctional γ-cyclodextrins having dansylcysteine and tosyl groups at two adjacent sugar units: synthesis and determination of regio-chemistry

Tetrahedron letters, 2007-04, Vol.48 (18), p.3267-3271

2007

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Preparation of 2A,3A-alloepimino-2A,3A-dideoxy-β-cyclodextrin as a versatile scaffold candidate for the hetero-2A,3A-bifunctionalization

Tetrahedron letters, 2005-02, Vol.46 (7), p.1115-1118

2005

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Selective functionalization of β-cyclodextrin: efficient conversions of 2,3- alloepoxypyranosides to 2,3- mannoepithiopyranosides

Tetrahedron letters, 2007-09, Vol.48 (38), p.6665-6668

2007

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Hetero-bifunctionalization of the secondary face of β-cyclodextrin: selective 3G-sulfonylation and subsequent 2G,3G-epoxidation of 3A-azido-3A-deoxy-altro-β-cyclodextrin

Tetrahedron letters, 2006-09, Vol.47 (37), p.6599-6602

2006

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Shortcut Synthesis of β-Cyclomannin from β-Cyclodextrin

Organic letters, 2006-12, Vol.8 (25), p.5733-5736

2006

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Selective modification of β-cyclodextrin: an unexpected tandem reaction enables the cross-linking of C2A and C2B via a sulfur atom

Chemical communications (Cambridge, England), 2007-07 (30), p.3157

2007

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Hetero-bifunctionalization of the secondary face of β-cyclodextrin: selective 3 G-sulfonylation and subsequent 2 G,3 G-epoxidation of 3 A-azido-3 A-deoxy- altro-β-cyclodextrin

Tetrahedron letters, 2006, Vol.47 (37), p.6599-6602

2006

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Selective synthesis and ester cleavage property of 3A,2B-anhydro-3B-deoxy-3B-thio-β-cyclodextrin

Tetrahedron letters, 2007-10, Vol.48 (42), p.7493-7497

2007

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The first hetero-bifunctionalization of the secondary face of beta-cyclodextrin: selective and efficient conversion of the A-ring of a 2A,2B-disulfonate to 2A,3A-epoxymannoside

Chemical communications (Cambridge, England), 2005-07 (25), p.3168

2005

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Clockwise-counterclockwise differentiation on the upper rim of a monofunctional gamma-cyclodextrin: efficient topological control in the syntheses of capped cyclodextrins

Chemical communications (Cambridge, England), 2006-01 (48), p.5057-5059

2006

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Selective synthesis and ester cleavage property of 3 A,2 B-anhydro-3 B-deoxy-3 B-thio-β-cyclodextrin

Tetrahedron letters, 2007, Vol.48 (42), p.7493-7497

2007

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Preparation of 2 A,3 A-alloepimino-2 A,3 A-dideoxy-β-cyclodextrin as a versatile scaffold candidate for the hetero-2 A,3 A-bifunctionalization

Tetrahedron letters, 2005-02, Vol.46 (7), p.1115-1118

2005

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Imidazolyl Cyclodextrins: Artificial Serine Proteases Enabling Regiospecific Reactions

Angewandte Chemie, 2007-06, Vol.119 (26), p.5112-5115

2007

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Cucurbit[7]uril: Synthesis and quenching the quorum sensing in bacteria

Functionalization of Cyclodextrins via Reactions of 2,3-Anhydrocyclodextrins

Three‐in‐One: Miniature Models of Natural Acyl‐Transfer Systems Enable Vector‐Selective Reaction on the Primary Side of Cyclodextrins

A one-pot synthetic method for the hetero-bifunctionalization of α-cyclodextrin at the secondary hydroxyl side with high clockwise-counterclockwise selectivity

Restriction of guest rotation based on the distortion of a cyclodextrin cavity

Synthesis and binding behaviors of monomethyl cucurbit[6]uril

Imidazolyl Cyclodextrins: Artificial Serine Proteases Enabling Regiospecific Reactions

Heptakis(6-deoxy-6-guanidino)-β-cyclodextrin: an artificial model for mitochondrial ADP/ATP carrier

A Vector-Selective Reaction Enables Efficient Construction of Specific Topology upon the Primary Side of β-Cyclodextrin

The first topologically controlled synthesis of doubly bridged beta-cyclodextrin dimers

Selective modification of beta-cyclodextrin: an unexpected tandem reaction enables the cross-linking of C2(A) and C2(B) via a sulfur atom

A facile sulfonylation method enabling direct syntheses of per(2- O-sulfonyl)-β-cyclodextrins

Hetero-bifunctional γ-cyclodextrins having dansylcysteine and tosyl groups at two adjacent sugar units: synthesis and determination of regio-chemistry

Preparation of 2A,3A-alloepimino-2A,3A-dideoxy-β-cyclodextrin as a versatile scaffold candidate for the hetero-2A,3A-bifunctionalization

Selective functionalization of β-cyclodextrin: efficient conversions of 2,3- alloepoxypyranosides to 2,3- mannoepithiopyranosides

Hetero-bifunctionalization of the secondary face of β-cyclodextrin: selective 3G-sulfonylation and subsequent 2G,3G-epoxidation of 3A-azido-3A-deoxy-altro-β-cyclodextrin

Shortcut Synthesis of β-Cyclomannin from β-Cyclodextrin

Selective modification of β-cyclodextrin: an unexpected tandem reaction enables the cross-linking of C2A and C2B via a sulfur atom

Hetero-bifunctionalization of the secondary face of β-cyclodextrin: selective 3 G-sulfonylation and subsequent 2 G,3 G-epoxidation of 3 A-azido-3 A-deoxy- altro-β-cyclodextrin

Selective synthesis and ester cleavage property of 3A,2B-anhydro-3B-deoxy-3B-thio-β-cyclodextrin

The first hetero-bifunctionalization of the secondary face of beta-cyclodextrin: selective and efficient conversion of the A-ring of a 2A,2B-disulfonate to 2A,3A-epoxymannoside

Clockwise-counterclockwise differentiation on the upper rim of a monofunctional gamma-cyclodextrin: efficient topological control in the syntheses of capped cyclodextrins

Selective synthesis and ester cleavage property of 3 A,2 B-anhydro-3 B-deoxy-3 B-thio-β-cyclodextrin

Preparation of 2 A,3 A-alloepimino-2 A,3 A-dideoxy-β-cyclodextrin as a versatile scaffold candidate for the hetero-2 A,3 A-bifunctionalization

Imidazolyl Cyclodextrins: Artificial Serine Proteases Enabling Regiospecific Reactions

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