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Synthesis of Pentahydroxy Indolizidine Alkaloids Using Ring Closing Metathesis: Attempts To Find the Correct Structure of Uniflorine A

Journal of organic chemistry, 2006-08, Vol.71 (16), p.6273-6276

2006

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Whole cell screen based identification of spiropiperidines with potent antitubercular properties

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (16), p.3234-3245

2015

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Intramolecular 5-endo-Trig Aminomercuration of β-Hydroxy-γ-alkenylamines: Efficient Route to a Pyrrolidine Ring and Its Application for the Synthesis of (+)-Castanospermine and Analogues

Journal of organic chemistry, 2006-06, Vol.71 (12), p.4667-4670

2006

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Asymmetric Dihydroxylation of d-Glucose Derived α,β-Unsaturated Ester: Synthesis of Azepane and Nojirimycin Analogues

Journal of organic chemistry, 2004-07, Vol.69 (14), p.4760-4766

2004

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Temporary Carbohydrate Diol Protection with Ester Groups – Orthogonality under Solid‐Phase Oligosaccharide Synthesis Conditions

European Journal of Organic Chemistry, 2009-10, Vol.2009 (29), p.5002-5011

2009

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Stereoselectivity in the Epoxidation of Carbohydrate-Based Oxepines

Journal of organic chemistry, 2008-08, Vol.73 (16), p.6341-6354

2008

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1,3-Dipolar Cycloaddition Reaction of d-Glucose-Derived Nitrone with Allyl Alcohol: Synthesis of 2-Hydroxy-1-deoxycastanospermine Analogues

Journal of organic chemistry, 2005-02, Vol.70 (4), p.1356-1363

2005

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Computational and experimental investigations of mono-septanoside binding by Concanavalin A: correlation of ligand stereochemistry to enthalpies of binding

Organic & biomolecular chemistry, 2011-01, Vol.9 (1), p.154-164

2011

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Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy- d- gluco-homonojirimycin and N-butyl 1-deoxy- l- ido-homonojirimycin

Bioorganic & medicinal chemistry, 2006-08, Vol.14 (16), p.5535-5539

2006

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Polyhydroxylated homoazepanes and 1-deoxy-homonojirimycin analogues: Synthesis and glycosidase inhibition study

Organic & biomolecular chemistry, 2006-01, Vol.4 (19), p.3675

2006

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Synthesis of tetrahydroxy perhydroaza-azulenes: tandem Johnson-Claisen rearrangement of D-glucose-derived allylic alcohols

Organic & biomolecular chemistry, 2006-01, Vol.4 (13), p.2549-2555

2006

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Discovery of Imidazo[1,2‑a]pyridine Ethers and Squaramides as Selective and Potent Inhibitors of Mycobacterial Adenosine Triphosphate (ATP) Synthesis

Journal of medicinal chemistry, 2017-02, Vol.60 (4), p.1379-1399

2017

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Hydroxyl group orientation affects hydrolysis rates of methyl α-septanosides

Tetrahedron letters, 2010-02, Vol.51 (8), p.1209-1212

2010

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Novel lead generation of an anti-tuberculosis agent active against non-replicating mycobacteria: exploring hybridization of pyrazinamide with multiple fragments

Medicinal chemistry research, 2015-07, Vol.24 (7), p.2986-2992

2015

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Scaffold morphing leading to evolution of 2,4-diaminoquinolines and aminopyrazolopyrimidines as inhibitors of the ATP synthesis pathway

MedChemComm, 2016, Vol.7 (5), p.1022-1032

2016

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Computational and experimental investigations of mono-septanoside binding by Concanavalin A: correlation of ligand stereochemistry to enthalpies of bindingElectronic supplementary information (ESI) available: 1H and 13C NMR spectra for all newly reported compounds. Computed QM/MM structures not shown in the main text are provided. Further details on the thermodynamic cycle used in our calculations and approximations are also provided. See DOI: 10.1039/c0ob00425a

2010-12

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Scaffold morphing leading to evolution of 2,4-diaminoquinolines and aminopyrazolopyrimidines as inhibitors of the ATP synthesis pathwayThe authors declare no competing interests.Electronic supplementary information (ESI) available: Materials and methods, synthesis Schemes 1A and B, Fig. S1: 3D flexible superimposition of compounds 3h, 8d and 17a with bedaquiline, Fig. S2 and S3: 2D binding site interaction of inhibitors - bedaquiline, compounds 3h, 8d, 12 and 17a - at the ATPase binding site and

2016-05

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ChemInform Abstract: Carbohydrates to Azasugars: Synthesis and Glycosidase Inhibition Study

ChemInform, 2008-06, Vol.39 (23), p.no-no

2008

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Synthesis of Pentahydroxy Indolizidine Alkaloids Using Ring Closing Metathesis: Attempts To Find the Correct Structure of Uniflorine A

Whole cell screen based identification of spiropiperidines with potent antitubercular properties

Intramolecular 5-endo-Trig Aminomercuration of β-Hydroxy-γ-alkenylamines: Efficient Route to a Pyrrolidine Ring and Its Application for the Synthesis of (+)-Castanospermine and Analogues

Asymmetric Dihydroxylation of d-Glucose Derived α,β-Unsaturated Ester: Synthesis of Azepane and Nojirimycin Analogues

Temporary Carbohydrate Diol Protection with Ester Groups – Orthogonality under Solid‐Phase Oligosaccharide Synthesis Conditions

Stereoselectivity in the Epoxidation of Carbohydrate-Based Oxepines

1,3-Dipolar Cycloaddition Reaction of d-Glucose-Derived Nitrone with Allyl Alcohol: Synthesis of 2-Hydroxy-1-deoxycastanospermine Analogues

Computational and experimental investigations of mono-septanoside binding by Concanavalin A: correlation of ligand stereochemistry to enthalpies of binding

Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy- d- gluco-homonojirimycin and N-butyl 1-deoxy- l- ido-homonojirimycin

Polyhydroxylated homoazepanes and 1-deoxy-homonojirimycin analogues: Synthesis and glycosidase inhibition study

Synthesis of tetrahydroxy perhydroaza-azulenes: tandem Johnson-Claisen rearrangement of D-glucose-derived allylic alcohols

Discovery of Imidazo[1,2‑a]pyridine Ethers and Squaramides as Selective and Potent Inhibitors of Mycobacterial Adenosine Triphosphate (ATP) Synthesis

Hydroxyl group orientation affects hydrolysis rates of methyl α-septanosides

Novel lead generation of an anti-tuberculosis agent active against non-replicating mycobacteria: exploring hybridization of pyrazinamide with multiple fragments

Scaffold morphing leading to evolution of 2,4-diaminoquinolines and aminopyrazolopyrimidines as inhibitors of the ATP synthesis pathway

ChemInform Abstract: Carbohydrates to Azasugars: Synthesis and Glycosidase Inhibition Study

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