Search Results - "Tilve, Santosh G."
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Recent Developments in the Synthesis of Five- and Six-Membered Heterocycles Using Molecular Iodine
Published in Chemistry : a European journal (27-04-2012)“…Heterocyclic scaffolds represent the key structural subunits of many biologically active compounds. Over the last few years iodine‐mediated reactions have been…”
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2
Domino Bischler–Napieralski – Michael Reaction and Oxidation – New Route to Coumarin‐Pyrrole‐Isoquinoline Fused Pentacycles
Published in European journal of organic chemistry (19-12-2018)“…Lamellarin scaffold is synthesized by a metal free convergent route involving domino Bischler–Napieralski reaction – Michael reaction – oxidation sequence. Six…”
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3
An efficient synthesis of indoloquinoline alkaloid—neocryptolepine (cryptotackieine)
Published in Tetrahedron letters (07-12-2011)“…A short and convenient method for the synthesis of neocryptolepine (cryptotackieine) is described using Wittig reaction and one-pot…”
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4
Total Synthesis of (−)- and (+)-Tedanalactam
Published in Journal of organic chemistry (21-08-2009)“…The first stereoselective route providing access to both enantiomers of tedanalactam, a naturally occurring piperidone, has been developed. The stereogenic…”
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5
Synthetic access to thiolane-based therapeutics and biological activity studies
Published in European journal of medicinal chemistry (15-11-2021)“…Secondary metabolites isolated from bioactive extracts of natural sources iteratively pioneer the research in drug discovery. Modern medicine is often inspired…”
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6
Iodine-Mediated Intramolecular Dehydrogenative Coupling: Synthesis of N‑Alkylindolo[3,2‑c]- and -[2,3‑c]quinoline Iodides
Published in Organic letters (04-03-2016)“…An I2/TBHP-mediated intramolecular dehydrogenative coupling reaction is developed for the synthesis of a library of medicinally important…”
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7
P4O10/TfOH mediated domino condensation–cyclization of amines with diacids: a route to indolizidine alkaloids under catalyst- and solvent-free conditions
Published in RSC advances (15-06-2022)“…A domino condensation–cyclization method is developed to synthesize indolizidine alkaloids using a P4O10/TfOH reagent system without the employment of either a…”
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Intramolecular Diels–Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds
Published in Tetrahedron (06-05-2014)“…[Display omitted]…”
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9
Graphite catalyzed solvent free synthesis of dihydropyrimidin-2(1H)-ones/thiones and their antidiabetic activity
Published in Bioorganic & medicinal chemistry letters (01-07-2014)“…A solvent free three component condensation reaction between an aldehyde, ethyl acetoacetate and urea catalyzed by graphite, a green catalyst is described for…”
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10
α-Glucosidase inhibition activity and in silico study of 2-(benzo[d][1,3]dioxol-5-yl)-4H-chromen-4-one, a synthetic derivative of flavone
Published in Bioorganic & medicinal chemistry (15-06-2019)“…[Display omitted] •BDC, a flavone derivative showed 22.4 fold higher enzyme inhibition than acarbose.•During the enzyme kinetic study BDC showed…”
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Synthetic access to syn-functionalised chiral hydroxy pyrrolidines and pyrrolidones: Evaluation of α-glucosidase inhibition activity, docking studies and pharmacokinetics prediction
Published in Bioorganic chemistry (01-12-2022)“…[Display omitted] •New chiral hydroxy pyrrolidines and pyrrolidones are synthesized via cross aldol reaction.•The hydroxy pyrrolidines are more potent than…”
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12
An Alternate Synthesis of 6H-Indolo[2,3-b]quinoline via One-Pot Alkylation-Dehydration-Cyclization-Aromatization Approach
Published in Journal of heterocyclic chemistry (01-11-2016)“…A simple, straightforward and efficient synthesis of 6H‐indolo[2,3‐b]quinoline, a natural product isolated from leaves of Justicia betonica, is achieved…”
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13
Synthesis of (−)-hygrine, (−)-norhygrine, (−)-pseudohygroline and (−)-hygroline via Nef reaction
Published in Tetrahedron letters (07-12-2011)“…Synthesis of tropane alkaloids (−)-hygrine, (−)-norhygrine and sedum alkaloids (−)-pseudohygroline and (−)-hygroline is described from l-proline via Henry and…”
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14
Graphite catalyzed green synthesis of quinoxalines
Published in Tetrahedron letters (01-02-2013)“…A new simple approach using environmentally benign, cheap, and easily recyclable graphite as a heterogeneous catalyst for the synthesis of quinoxalines is…”
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15
Pyrrolidine and iodine catalyzed domino aldol-Michael-dehydrogenative synthesis of flavones
Published in Tetrahedron letters (28-05-2014)“…A one pot synthesis of flavones is established from 2′-hydroxyacetophenones and substituted aromatic aldehydes. The method uses domino aldol-Michael-oxidation…”
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16
Molecular iodine catalyst promoted synthesis of chromans and 4-aryl-3,4-dihydrobenzopyran-2-ones via [3+3] cyclocoupling
Published in Tetrahedron (26-08-2014)“…Molecular iodine as an inexpensive catalyst is described in the construction of 2-substituted or 2,2-disubstituted chromans and…”
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17
Tandem approaches for the synthesis of functionalized pyrrolidones: efficient routes toward allokainic acid and kainic acid
Published in Tetrahedron letters (01-01-2013)“…Tandem approaches for the synthesis of pyrrolidone precursor of allokainic acid and kainic acid are described. The synthesis of pyrrolidone intermediate of…”
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18
An Expeditious I2-Catalyzed Entry into 6H-Indolo[2,3-b]quinoline System of Cryptotackieine
Published in Journal of organic chemistry (06-11-2009)“…A synthesis of a series of novel 6H-indolo[2,3-b]quinolines with different substituents on the quinoline ring is described. The method involves reaction of…”
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Convenient and efficient syntheses of 4-hydroxy-2(E)-nonenal and 4-oxo-2(E)-nonenal
Published in Lipids (01-09-2006)“…Lipid peroxidation products 4-hydroxy-2(E)-nonenal (HNE) and 4-oxo-2(E)-nonenal (ONE) were conveniently synthesized using Wittig and Horner-Wardsworth-Emmons…”
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20
Solventless Mechanosynthesis Of Bis(Indolyl)Methanes
Published in Synthetic communications (02-01-2019)“…Ball-milling technique as a solvent-free and an alternative green process was investigated for the eco-benign synthesis of bis(indolyl)methanes (BIMs) from…”
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