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Anil V. Karnik
Anil V. Karnik
Department of Chemistry, University of Mumbai
在 chem.mu.ac.in 的电子邮件经过验证
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引用次数
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Furo-fused BINOL based crown as a fluorescent chiral sensor for enantioselective recognition of phenylethylamine and ethyl ester of valine
SP Upadhyay, RRS Pissurlenkar, EC Coutinho, AV Karnik
The Journal of Organic Chemistry 72 (15), 5709-5714, 2007
742007
Synthesis and in vitro anti-bacterial evaluation of tetracyclic-ortho-fused 4H-naphtho [1′, 2′–5, 6] pyrano [3, 4-d](1, 2, 3) selenadiazole and its derivatives
AV Karnik, AM Kulkarni, NJ Malviya, BR Mourya, BL Jadhav
European journal of medicinal chemistry 43 (11), 2615-2617, 2008
582008
Enantioselective Benzoylation of α-Amino Esters Using (S)-1-Benzoyl-2- (α-acetoxyethyl)benzimidazole, a Chiral Benzimidazolide
AV Karnik, SS Kamath
The Journal of Organic Chemistry 72 (19), 7435-7438, 2007
502007
Enantioselective benzoylation of racemic amines using chiral benzimidazolide as a benzoylating agent
AV Karnik, SS Kamath
Tetrahedron: Asymmetry 19 (1), 45-48, 2008
492008
Synthesis and in vitro antibacterial activity of novel heterocyclic derivatives of 18-nor-equilenin
AV Karnik, NJ Malviya, AM Kulkarni, BL Jadhav
European journal of medicinal chemistry 41 (7), 891-895, 2006
312006
Facile conversion of acyldiithiocarbazinate salts to 1, 3, 4-oxadiazole derivatives under microwave irradiation
S Joshi, AV Karnik
Synthetic communications 32 (1), 111-114, 2002
272002
Chiral benzimidazoles and their applications in stereodiscrimination processes
VN Khose, ME John, AD Pandey, AV Karnik
Tetrahedron: Asymmetry 28 (10), 1233-1289, 2017
252017
Tailor-Made Supramolecular Chirogenic System Based on Cs-Symmetric Rigid Organophosphoric Acid Host and Amino Alcohols: Mechanistic Studies, Bulkiness …
M Hasan, VN Khose, AD Pandey, V Borovkov, AV Karnik
Organic letters 18 (3), 440-443, 2016
202016
Sterically Congested Chiral 7, 8‐Dioxa [6] helicene and Its Dihydro Analogues: Synthesis, Regioselective Functionalization, and Unexpected Domino Prins Reaction
M Hasan, AD Pandey, VN Khose, NA Mirgane, AV Karnik
European Journal of Organic Chemistry 2015 (17), 3702-3712, 2015
192015
Sui generis helicene-based supramolecular chirogenic system: Enantioselective sensing, solvent control, and application in chiral group transfer reaction
M Hasan, VN Khose, T Mori, V Borovkov, AV Karnik
ACS omega 2 (2), 592-598, 2017
182017
Rapid and efficient microwave-assisted synthesis of 4-amino-3-mercapto-5-substituted-1, 2, 4-triazoles
SS Joshi, AV Karnik
NISCAIR-CSIR, India, 2006
182006
Stereochemistry: a three-dimensional insight
AV Karnik, M Hasan
Elsevier, 2021
162021
Chiral heterocycle-based receptors for enantioselective recognition
VN Khose, ME John, AD Pandey, V Borovkov, AV Karnik
Symmetry 10 (2), 34, 2018
152018
A convenient route to optically active γ-substituted γ-lactones
AV Karnik, ST Patil, SS Patnekar, A Semwal
New Journal of Chemistry 28 (12), 1420-1422, 2004
152004
Directional approach to enantiomerically enriched functionalized [7] Oxa-helicenoids and groove-based selective cyanide sensing
VN Khose, M Hasan, SC Khot, SM Mobin, V Borovkov, AV Karnik
The Journal of Organic Chemistry 85 (4), 1847-1860, 2019
142019
Chiral benzimidazole-derived mono azacrowns: synthesis and enantiomer recognition studies with chiral amines and their ammonium salts
A Pandey, H Mohammed, A Karnik
Tetrahedron: Asymmetry 24 (12), 706-712, 2013
142013
[9, 9′] Bi [naphtho (2, 1-b) furanyl]-8, 8′-diol, a furo-fused BINOL derivative: synthesis, resolution and determination of absolute configuration
AV Karnik, SP Upadhyay, MG Gangrade
Tetrahedron: Asymmetry 17 (8), 1275-1280, 2006
142006
Aqueous ethanol: a suitable medium for the diastereoselective Diels–Alder reaction mediated by chiral bases
NA Mirgane, AV Karnik
Green Chemistry Letters and Reviews 4 (3), 269-272, 2011
132011
Asymmetric Diels–Alder reaction involving chiral benzimidazoles as organocatalysts
NA Mirgane, AV Karnik
Chirality 23 (5), 404-407, 2011
132011
Ionic liquid promoted Diels-Alder Reaction between anthrone and maleimides
N Mirgane, S Kotwal, A Karnik
Open Chemistry 8 (2), 356-360, 2010
132010
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