Bhalchandra M. Bhanage

Affiliations: 
Chemistry Institute of Chemical Technology, Mumbai 
Area:
Homogeneous catalysis
Website:
http://bmbhanage.weebly.com/
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"Bhalchandra Bhanage"
Mean distance: 11375.1
 
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Publications

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Lokolkar MS, Jagtap PA, Bhanage BM. (2024) Pd-catalysed synthesis of oxomalonamides through adjacent triple carbonylation of tertiary amines. Chemical Communications (Cambridge, England). 60: 5411-5414
Mourya B, Gadge ST, Bhanage BM. (2024) The synthesis of alk-2-ynl Weinreb amides Pd/Cu-catalysed oxidative carbonylation of terminal alkynes. Organic & Biomolecular Chemistry
Badgujar KC, Badgujar JK, Bhanage BM. (2024) Improved biocatalytic activity of steapsin lipase in supercritical carbon dioxide medium for the synthesis of benzyl butyrate: A commercially important flavour compound. Journal of Biotechnology. 384: 55-62
Jagtap PA, Lokolkar MS, Bhanage BM. (2023) Cu-Mediated Tandem 2,3-Disubstituted Indole Synthesis from Simple Anilines and Internal Alkynes C-H Annulation. The Journal of Organic Chemistry
Nabar KU, Bhanage BM, Dawande SG. (2023) Copper-catalyzed -arylation of amines with aryliodonium ylides in water. Beilstein Journal of Organic Chemistry. 19: 1008-1014
Kolekar YA, Saptal VB, Bhanage BM. (2023) Carbonylative Self-Coupling of Aryl Boronic Acids Using a Confined Pd Catalyst within Melamine Dendron and Fibrous Nano-Silica: A CO Surrogate Approach. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301381
Mishra AA, Bhanage BM. (2021) Ru-TsDPEN catalysts and derivatives in asymmetric transfer hydrogenation reactions. Chirality
Kolekar YA, Bhanage BM. (2021) Pd-Catalyzed Oxidative Aminocarbonylation of Arylboronic Acids with Unreactive Tertiary Amines via C-N Bond Activation. The Journal of Organic Chemistry
Jawale PV, Bhanage BM. (2020) Synthesis of propyl benzoate by solvent-free immobilized lipase-catalyzed transesterification: Optimization and kinetic modeling. Bioprocess and Biosystems Engineering
Mishra AA, Chaurasia SR, Bhanage BM. (2020) Ru–g-C3N4 as a highly active heterogeneous catalyst for transfer hydrogenation of α-keto amide into β-aminol or α-hydroxyl amide New Journal of Chemistry. 44: 10578-10585
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