Search Results - "Markad, Shankar D"
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1
Synthesis of Pentahydroxy Indolizidine Alkaloids Using Ring Closing Metathesis: Attempts To Find the Correct Structure of Uniflorine A
Published in Journal of organic chemistry (04-08-2006)“…Ring closing metathesis of d-glucose derived diene-substrate containing nitrogen functionality followed by asymmetric dihydroxylation afforded sugar…”
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2
Whole cell screen based identification of spiropiperidines with potent antitubercular properties
Published in Bioorganic & medicinal chemistry letters (15-08-2015)“…[Display omitted] Whole cell based screens to identify hits against Mycobacterium tuberculosis (Mtb), carried out under replicating and non-replicating (NRP)…”
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3
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
Published in Journal of organic chemistry (09-06-2006)“…The intramolecular aminomercuration reaction of sugar-derived β-hydroxy-γ-alkenylamines 8a−c undergoes 5-endo-trig cyclization in high yield. The…”
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4
Temporary Carbohydrate Diol Protection with Ester Groups – Orthogonality under Solid‐Phase Oligosaccharide Synthesis Conditions
Published in European Journal of Organic Chemistry (01-10-2009)“…For regioselective deprotection studies under SPOS conditions the glucosamine derivatives 4ab/4ba, 4ac/4ca and 4ad/4da – with Fmoc/PA, Fmoc/Lev or Fmoc/Alloc,…”
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Book Review Journal Article -
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Asymmetric Dihydroxylation of d-Glucose Derived α,β-Unsaturated Ester: Synthesis of Azepane and Nojirimycin Analogues
Published in Journal of organic chemistry (09-07-2004)“…The asymmetric dihydroxylation of a d-glucose derived α,β-unsaturated ester 3 afforded syn vicinal diols in good to high diastereoselectivity. The conversion…”
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6
Stereoselectivity in the Epoxidation of Carbohydrate-Based Oxepines
Published in Journal of organic chemistry (15-08-2008)“…The facial selectivity in the DMDO epoxidation of carbohydrate-based oxepines derived from glucose, galactose, and mannose has been determined by product…”
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7
Computational and experimental investigations of mono-septanoside binding by Concanavalin A: correlation of ligand stereochemistry to enthalpies of binding
Published in Organic & biomolecular chemistry (01-01-2011)“…Structure-energy relationships for a small group of pyranose and septanose mono-saccharide ligands are developed for binding to Concanavalin A (ConA). The…”
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8
1,3-Dipolar Cycloaddition Reaction of d-Glucose-Derived Nitrone with Allyl Alcohol: Synthesis of 2-Hydroxy-1-deoxycastanospermine Analogues
Published in Journal of organic chemistry (18-02-2005)“…The synthesis and evaluation of glycosidase inhibitory activity of polyhydroxylated indolizidine alkaloids namely 2-hydroxy-1-deoxycastanospermine 3a,b and…”
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9
Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy- d- gluco-homonojirimycin and N-butyl 1-deoxy- l- ido-homonojirimycin
Published in Bioorganic & medicinal chemistry (15-08-2006)“…Conjugate addition of n-butyl amine to d-glucose derived α,β-unsaturated ester 4 afforded β-amino esters 5a, b that on reduction of ester group, 1,2-acetonide…”
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10
Polyhydroxylated homoazepanes and 1-deoxy-homonojirimycin analogues: Synthesis and glycosidase inhibition study
Published in Organic & biomolecular chemistry (01-01-2006)“…The Johnson-Claisen rearrangement of D-gluco and L-ido-derived allylic orthoesters afforded gamma,delta-unsaturated ester that on ester reduction, epoxidation,…”
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11
Discovery of Imidazo[1,2‑a]pyridine Ethers and Squaramides as Selective and Potent Inhibitors of Mycobacterial Adenosine Triphosphate (ATP) Synthesis
Published in Journal of medicinal chemistry (23-02-2017)“…The approval of bedaquiline to treat tuberculosis has validated adenosine triphosphate (ATP) synthase as an attractive target to kill Mycobacterium…”
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12
Hydroxyl group orientation affects hydrolysis rates of methyl α-septanosides
Published in Tetrahedron letters (24-02-2010)“…Hydrolysis rates for three related methyl α-septanosides were obtained. The septanosides were synthesized via mCPBA epoxidation and methanolysis of d-mannose,…”
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13
Novel lead generation of an anti-tuberculosis agent active against non-replicating mycobacteria: exploring hybridization of pyrazinamide with multiple fragments
Published in Medicinal chemistry research (01-07-2015)“…The key to shortening tuberculosis (TB) drug regimen lies in eliminating the reservoir of non-replicating persistent (NRP) Mycobacterium tuberculosis (Mtb)…”
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