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Conformationally-constrained indeno[2,1-c]quinolines--a new class of anti-mycobacterial agents

Organic & biomolecular chemistry, 2010-01, Vol.8 (9), p.2180-2197

2010

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Structural Basis of α-Fucosidase Inhibition by Iminocyclitols with Ki Values in the Micro- to Picomolar Range

Angewandte Chemie (International ed.), 2010-01, Vol.49 (2), p.337-340

2010

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Synthesis and antimycobacterial activity of prodrugs of indeno[2,1- c]quinoline derivatives

European journal of medicinal chemistry, 2011-04, Vol.46 (4), p.1306-1324

2011

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Novel quinoline and naphthalene derivatives as potent antimycobacterial agents

European journal of medicinal chemistry, 2010-05, Vol.45 (5), p.1854-1867

2010

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Structural Basis of α‐Fucosidase Inhibition by Iminocyclitols with K i Values in the Micro‐ to Picomolar Range

Angewandte Chemie International Edition, 2010-01, Vol.49 (2), p.337-340

2010

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Synthesis and structure of azole-fused indeno[2,1-c]quinolines and their anti-mycobacterial properties

Organic & biomolecular chemistry, 2010-01, Vol.8 (24), p.5661-5673

2010

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Development of GlcNAc-Inspired Iminocyclitiols as Potent and Selective N-Acetyl-β-Hexosaminidase Inhibitors

ACS chemical biology, 2010-05, Vol.5 (5), p.489-497

2010

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Structural and Thermodynamic Analyses of α-L-Fucosidase Inhibitors

Chembiochem : a European journal of chemical biology, 2010-09, Vol.11 (14), p.1971-1974

2010

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Synthesis and Evaluation of 4/5-Hydroxy-2,3-diaryl(substituted)-cyclopent-2-en-1-ones as cis-Restricted Analogues of Combretastatin A-4 as Novel Anticancer Agents

Journal of medicinal chemistry, 2007-04, Vol.50 (8), p.1744-1753

2007

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Li–X-type zeolite mediated Michael addition of thiols to cyclic enones and its application in the synthesis of 13-thiaprostaglandins

Journal of molecular catalysis. A, Chemical, 2004-07, Vol.216 (1), p.115-119

2004

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EPZ-10 catalyzed regioselective transformation of alkenes into β-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans

Green chemistry : an international journal and green chemistry resource : GC, 2002-01, Vol.4 (4), p.325-327

2002

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A convenient oxidative demasking of 1,3-dithiolanes and dithianes to carbonyl compounds with TBHP

Tetrahedron letters, 2002-08, Vol.43 (34), p.6031-6033

2002

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Thioacetalization of the carbonyl function, transthioacetalization of acetals, ketals, oximes and hydrazones catalysed by aqueous hydrobromic acid

ARKIVOC, 2004-09, Vol.2004 (14), p.110-117

2004

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Enzymatic kinetic resolution studies of racemic 4-hydroxycyclopent-2-en-1-one using Lipozyme IM

Tetrahedron: asymmetry, 1999-10, Vol.10 (21), p.4115-4122

1999

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Cover Picture: Structural and Thermodynamic Analyses of α-L-Fucosidase Inhibitors (ChemBioChem 14/2010)

Chembiochem : a European journal of chemical biology, 2010-09, Vol.11 (14), p.1925-1925

2010

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Synthesis and structure of azole-fused indeno[2,1-c]quinolines and their anti-mycobacterial propertiesElectronic supplementary information (ESI) available: Spectral data (1D-NMR, 2D-NMR, LCMS, Mass, HPLC and IR) for all new compounds is included. See DOI: 10.1039/c0ob00445f

2010-12

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Structural Basis of α‐Fucosidase Inhibition by Iminocyclitols with K i Values in the Micro‐ to Picomolar Range

Angewandte Chemie, 2010-01, Vol.122 (2), p.347-350

2010

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Convenient synthesis of 5-methylene-4-substituted-2(5 H)-furanones

Tetrahedron letters, 2005-02, Vol.46 (6), p.1009-1012

2005

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Studies on Bromination of Active Methylene by a Mixture of Hydrobromic Acid and Hydrogen Peroxide (or TBHP)

Synthetic communications, 2003-01, Vol.33 (8), p.1399-1403

2003

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Structural basis of alpha-fucosidase inhibition by iminocyclitols with K(i) values in the micro- to picomolar range

Angewandte Chemie International Edition, 2010, Vol.49 (2), p.337-340

2010

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Structural Basis of α-Fucosidase Inhibition by Iminocyclitols with Ki Values in the Micro- to Picomolar Range

Angewandte Chemie, 2010-01, Vol.122 (2), p.347-350

2010

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EPZ-10 catalyzed regioselective transformation of alkenes into [small beta]-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans

Green chemistry : an international journal and green chemistry resource : GC, 2002-01, Vol.4 (4), p.325-327

2002

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Convenient Synthesis of 5-Methylene-4-substituted-2(5H)-furanones

ChemInform, 2005-05, Vol.36 (22), p.no-no

2005

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Studies on Bromination of Active Methylene by a Mixture of Hydrobromic Acid and Hydrogen Peroxide (or TBHP)

ChemInform, 2003-08, Vol.34 (34), p.no-no

2003

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A Convenient Oxidative Demasking of 1,3-Dithiolanes and Dithianes to Carbonyl Compounds with TBHP

ChemInform, 2002-11, Vol.33 (46), p.75-75

2002

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Conformationally-constrained indeno[2,1-c]quinolines--a new class of anti-mycobacterial agents

Structural Basis of α-Fucosidase Inhibition by Iminocyclitols with Ki Values in the Micro- to Picomolar Range

Synthesis and antimycobacterial activity of prodrugs of indeno[2,1- c]quinoline derivatives

Novel quinoline and naphthalene derivatives as potent antimycobacterial agents

Structural Basis of α‐Fucosidase Inhibition by Iminocyclitols with K i Values in the Micro‐ to Picomolar Range

Synthesis and structure of azole-fused indeno[2,1-c]quinolines and their anti-mycobacterial properties

Development of GlcNAc-Inspired Iminocyclitiols as Potent and Selective N-Acetyl-β-Hexosaminidase Inhibitors

Structural and Thermodynamic Analyses of α-L-Fucosidase Inhibitors

Synthesis and Evaluation of 4/5-Hydroxy-2,3-diaryl(substituted)-cyclopent-2-en-1-ones as cis-Restricted Analogues of Combretastatin A-4 as Novel Anticancer Agents

Li–X-type zeolite mediated Michael addition of thiols to cyclic enones and its application in the synthesis of 13-thiaprostaglandins

EPZ-10 catalyzed regioselective transformation of alkenes into β-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans

A convenient oxidative demasking of 1,3-dithiolanes and dithianes to carbonyl compounds with TBHP

Thioacetalization of the carbonyl function, transthioacetalization of acetals, ketals, oximes and hydrazones catalysed by aqueous hydrobromic acid

Enzymatic kinetic resolution studies of racemic 4-hydroxycyclopent-2-en-1-one using Lipozyme IM

Cover Picture: Structural and Thermodynamic Analyses of α-L-Fucosidase Inhibitors (ChemBioChem 14/2010)

Synthesis and structure of azole-fused indeno[2,1-c]quinolines and their anti-mycobacterial propertiesElectronic supplementary information (ESI) available: Spectral data (1D-NMR, 2D-NMR, LCMS, Mass, HPLC and IR) for all new compounds is included. See DOI: 10.1039/c0ob00445f

Structural Basis of α‐Fucosidase Inhibition by Iminocyclitols with K i Values in the Micro‐ to Picomolar Range

Convenient synthesis of 5-methylene-4-substituted-2(5 H)-furanones

Studies on Bromination of Active Methylene by a Mixture of Hydrobromic Acid and Hydrogen Peroxide (or TBHP)

Structural basis of alpha-fucosidase inhibition by iminocyclitols with K(i) values in the micro- to picomolar range

Structural Basis of α-Fucosidase Inhibition by Iminocyclitols with Ki Values in the Micro- to Picomolar Range

EPZ-10 catalyzed regioselective transformation of alkenes into [small beta]-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans

Convenient Synthesis of 5-Methylene-4-substituted-2(5H)-furanones

Studies on Bromination of Active Methylene by a Mixture of Hydrobromic Acid and Hydrogen Peroxide (or TBHP)

A Convenient Oxidative Demasking of 1,3-Dithiolanes and Dithianes to Carbonyl Compounds with TBHP

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