Search Results - "Tilve, Santosh G."

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  1. 1

    Recent Developments in the Synthesis of Five- and Six-Membered Heterocycles Using Molecular Iodine by Parvatkar, Prakash T., Parameswaran, Perunninakulath S., Tilve, Santosh G.

    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. 2

    Domino Bischler–Napieralski – Michael Reaction and Oxidation – New Route to Coumarin‐Pyrrole‐Isoquinoline Fused Pentacycles by Mandrekar, Ketan S., Kadam, Hari K., Tilve, Santosh G.

    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. 3

    An efficient synthesis of indoloquinoline alkaloid—neocryptolepine (cryptotackieine) by Parvatkar, Prakash T., Tilve, Santosh G.

    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. 4

    Total Synthesis of (−)- and (+)-Tedanalactam by Majik, Mahesh S, Parameswaran, Perunninakulath S, Tilve, Santosh G

    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. 5

    Synthetic access to thiolane-based therapeutics and biological activity studies by Rodrigues, Lima, Tilve, Santosh G., Majik, Mahesh S.

    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. 6

    Iodine-Mediated Intramolecular Dehydrogenative Coupling: Synthesis of N‑Alkylindolo[3,2‑c]- and -[2,3‑c]quinoline Iodides by Volvoikar, Prajesh S, Tilve, Santosh G

    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. 7

    P4O10/TfOH mediated domino condensation–cyclization of amines with diacids: a route to indolizidine alkaloids under catalyst- and solvent-free conditions by Mandrekar, Ketan S, Tilve, Santosh G

    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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  8. 8
  9. 9

    Graphite catalyzed solvent free synthesis of dihydropyrimidin-2(1H)-ones/thiones and their antidiabetic activity by Dhumaskar, Kashinath L, Meena, Surya Nandan, Ghadi, Sanjeev C, Tilve, Santosh G

    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. 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 by Meena, Surya N., kumar, Ujjwal, Naik, Mayuri M., Ghadi, Sanjeev C., Tilve, Santosh G.

    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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  11. 11

    Synthetic access to syn-functionalised chiral hydroxy pyrrolidines and pyrrolidones: Evaluation of α-glucosidase inhibition activity, docking studies and pharmacokinetics prediction by Mhaldar, Shashank N., Kotkar, Gayatri D., Tilve, Santosh G.

    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. 12

    An Alternate Synthesis of 6H-Indolo[2,3-b]quinoline via One-Pot Alkylation-Dehydration-Cyclization-Aromatization Approach by Kadam, Hari K., Tilve, Santosh G.

    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. 13

    Synthesis of (−)-hygrine, (−)-norhygrine, (−)-pseudohygroline and (−)-hygroline via Nef reaction by Bhat, Chinmay, Tilve, Santosh G.

    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. 14

    Graphite catalyzed green synthesis of quinoxalines by Kadam, Hari K., Khan, Salman, Kunkalkar, Rupesh A., Tilve, Santosh G.

    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. 15

    Pyrrolidine and iodine catalyzed domino aldol-Michael-dehydrogenative synthesis of flavones by Naik, Mayuri M., Tilve, Santosh G., Kamat, Vijayendra P.

    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. 16

    Molecular iodine catalyst promoted synthesis of chromans and 4-aryl-3,4-dihydrobenzopyran-2-ones via [3+3] cyclocoupling by Naik, Mayuri M., Kamat, Durga P., Tilve, Santosh G., Kamat, Vijayendra P.

    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. 17

    Tandem approaches for the synthesis of functionalized pyrrolidones: efficient routes toward allokainic acid and kainic acid by Bhat, Chinmay, Tilve, Santosh G.

    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. 18

    An Expeditious I2-Catalyzed Entry into 6H-Indolo[2,3-b]quinoline System of Cryptotackieine by Parvatkar, Prakash T, Parameswaran, Perunninakulath S, Tilve, Santosh G

    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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  19. 19

    Convenient and efficient syntheses of 4-hydroxy-2(E)-nonenal and 4-oxo-2(E)-nonenal by Kurangi, Reshma F, Tilve, Santosh G, Blair, Ian A

    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. 20

    Solventless Mechanosynthesis Of Bis(Indolyl)Methanes by Mhaldar, Shashank N., Mandrekar, Ketan S., Gawde, Mukund K., Shet, Rajdatt V., Tilve, Santosh G.

    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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