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Dive into the research topics where Chinmay Bhat is active.

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Featured researches published by Chinmay Bhat.


RSC Advances | 2014

Recent advances in the synthesis of naturally occurring pyrrolidines, pyrrolizidines and indolizidine alkaloids using proline as a unique chiral synthon

Chinmay Bhat; Santosh G. Tilve

The present article describes the synthesis of a wide spectrum of natural products of the class pyrrolidines, pyrrolizidines and indolizidines using proline as a viable synthetic precursor. The review emphasizes the versatility of the basic unit of proline as a useful chiral synthon confined for the synthesis of only natural products of the above mentioned families. The vast coverage of the synthesis of these natural products is presented for a period from 1990 onwards. The synthesis of all ranges of alkaloids from simple to complex molecules is presented under the groups of alkaloids.


RSC Advances | 2013

Magnetically recoverable catalytic Co–Co2B nanocomposites for the chemoselective reduction of aromatic nitro compounds

Amit A. Vernekar; Sagar Patil; Chinmay Bhat; Santosh G. Tilve

Magnetically recoverable and recyclable Co–Co2B nanocomposites are described for the catalytic and chemoselective reduction of nitroarenes using two different hydrogen sources, sodium borohydride and hydrazine hydrate. Both the systems display an interesting chemoselective reduction switch. The kinetics of reduction of nitroaromatics were studied for the first time and follow nitroreductase enzyme-like kinetics with exceedingly high Kcat (5.2 × 104 s−1) and Kcat/KM (4.4 × 106 M−1 s−1) values, reaching the state of catalytic perfection. The recyclability of the catalyst system was studied by magnetically recovering the nano composite catalyst.


Bioorganic & Medicinal Chemistry Letters | 2013

Synthesis of (R)-norbgugaine and its potential as quorum sensing inhibitor against Pseudomonas aeruginosa

Mahesh S. Majik; Deepak Naik; Chinmay Bhat; Santosh G. Tilve; Supriya Tilvi; Lisette D’Souza

(R)-Bgugaine is a natural pyrrolidine alkaloid from Arisarum vulgare, which shows antifungal and antibacterial activity. In this Letter, we have accomplished the simple synthesis of norbgugaine (demethylated form of natural bgugaine) employing Wittig olefination and cat. hydrogenation as the key steps and its biological studies are reported for the first time. The synthesized norbgugaine was evaluated for inhibition of quorum sensing mediated virulence factors (motility, biofilm formation, pyocyanin pigmentation, rhamnolipid production and LasA protease) in Pseudomonas aeruginosa wherein swarming motility is reduced by 95%, and biofilm formation by 83%.


Synthetic Communications | 2014

PDC-Mediated Tandem Oxidative–Wittig Olefination

Kashinath L. Dhumaskar; Chinmay Bhat; Santosh G. Tilve

Abstract A convenient tandem oxidative–Wittig olefination of a primary alcohols to α,β-unsaturated compounds using pyridinium dichromate (PDC) is described. GRAPHICAL ABSTRACT


Tetrahedron Letters | 2011

Synthesis of (−)-hygrine, (−)-norhygrine, (−)-pseudohygroline and (−)-hygroline via Nef reaction

Chinmay Bhat; Santosh G. Tilve


Tetrahedron | 2013

Henry–Nef reaction: a practical and versatile chiral pool route to 2-substituted pyrrolidine and piperidine alkaloids

Chinmay Bhat; Santosh G. Tilve


Synthesis | 2014

Conhydrine: An Account of Isolation, Biological Perspectives and Synthesis

Chinmay Bhat; Sandesh T. Bugde; Santosh G. Tilve


Tetrahedron Letters | 2013

Tandem approaches for the synthesis of functionalized pyrrolidones: efficient routes toward allokainic acid and kainic acid

Chinmay Bhat; Santosh G. Tilve


Tetrahedron | 2013

A concise diastereoselective approach to (+)-dexoxadrol, (−)-epi-dexoxadrol, (−)-conhydrine and (+)-lentiginosine from (−)-pipecolinic acid

Chinmay Bhat; Santosh G. Tilve


Archives of Microbiology | 2017

The first report on Listeria monocytogenes producing siderophores and responds positively to N-acyl homoserine lactone (AHL) molecules by enhanced biofilm formation

Milind Mohan Naik; Purva Bhangui; Chinmay Bhat

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