Subhajit Bhunia
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Explore the profile of Subhajit Bhunia including associated specialties, affiliations and a list of published articles.
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26
Citations
190
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Recent Articles
1.
Parsutkar M, Bhunia S, Majumder M, Lalisse R, Hadad C, RajanBabu T
J Am Chem Soc
. 2023 Mar;
145(13):7462-7481.
PMID: 36972549
Enantiopure homoallylic boronate esters are versatile intermediates because the C-B bond in these compounds can be stereospecifically transformed into C-C, C-O, and C-N bonds. Regio- and enantioselective synthesis of these...
2.
Bhunia S, Pena-Duarte A, Li H, Li H, Sanad M, Saha P, et al.
ACS Nano
. 2023 Feb;
17(4):3492-3505.
PMID: 36753696
Designing N-coordinated porous single-atom catalysts (SACs) for the oxygen reduction reaction (ORR) is a promising approach to achieve enhanced energy conversion due to maximized atom utilization and higher activity. Here,...
3.
Bhunia S, Saha P, Moitra P, Addicoat M, Bhattacharya S
Chem Sci
. 2022 Jul;
13(26):7920-7932.
PMID: 35865887
Solid porous and crystalline covalent organic frameworks (COFs) are characterized by their higher specific BET surface areas and functional pore walls, which allow the adsorption of various bioactive molecules inside...
4.
Bhunia S, De S, Ma D
Org Lett
. 2022 Jan;
24(5):1253-1257.
PMID: 35099979
,'-Bis(pyridin-2-ylmethyl)oxalamide (BPMO) was found to be an apposite promoter for the Cu-catalyzed -arylation of oxazolidinones and primary and secondary amides with (hetero)aryl iodides at room temperature. Excellent chemoselectivity reached between...
5.
Bhunia S, Bhunia K, Patra B, Das S, Pradhan D, Bhaumik A, et al.
ACS Appl Mater Interfaces
. 2018 Dec;
11(1):1520-1528.
PMID: 30547587
Oxygen evolution reaction (OER) is energetically challenging from the platform of making many photovoltaic devices such as metal-air batteries and water splitting systems because of its poor kinetics even when...
6.
Bhunia S, Dey N, Pradhan A, Bhattacharya S
Chem Commun (Camb)
. 2018 Jun;
54(54):7495-7498.
PMID: 29922790
A donor-acceptor based conjugated microporous polymer, PER@NiP-CMOP-1, has been synthesized which can achieve highly sensitive stereo-specific "Turn ON" biosensing of an aminoglycoside up to the ppb level. The coordination-driven inhibition...
7.
Bhunia S, Chaudhuri S, De S, Babu K, Bisai A
Org Biomol Chem
. 2018 Mar;
16(14):2427-2437.
PMID: 29556598
The synthesis of the tetracyclic skeleton of ergot alkaloids has been developed via a key organocatalytic enantioselective aldol reaction using paraformaldehyde as the C1-unit in the presence of thiourea catalyst...
8.
Chaudhuri S, Ghosh S, Bhunia S, Bisai A
Chem Commun (Camb)
. 2018 Jan;
54(8):940-943.
PMID: 29318233
We report an expeditious catalytic asymmetric approach to clavine alkaloids via a key Heck cyclization. This reaction sets the formation of vicinal stereocenters with excellent diastereoselectivity. Utilizing the aforementioned strategy,...
9.
Chaudhuri S, Bhunia S, Roy A, Das M, Bisai A
Org Lett
. 2017 Dec;
20(1):288-291.
PMID: 29235356
Biomimetic total syntheses of either enantiomers of a number of ergot alkaloids, chanoclavine I (1b), chanoclavine I aldehyde (1c), pyroclavine (1e), festuclavine (1f), pibocin A (1g), 9-deacetoxyfumigaclavine C (1h), and...
10.
Bhunia S, Kumar S, Ma D
J Org Chem
. 2017 Nov;
82(23):12603-12612.
PMID: 29117476
N,N'-Bis(furan-2-ylmethyl)oxalamide (BFMO), an inexpensive and conveniently available bidentate ligand, is very effective for promoting Cu-catalyzed N-arylation of anilines and cyclic secondary amines. The method enables coupling of a broad range...