Swadhin K. Mandal

Affiliations: 
2007- IISER Kolkata 
Area:
Organometallic chemistry
Website:
http://swadhin-mandal.weebly.com/
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"Swadhin K. Mandal"
Bio:

(born 1973)

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Parents

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Setharampattu Seshaiyer Krishnamurthy grad student 1996-2002 IISc Bangalore
 (Palladium Complexes of P, P - , P, N - , and P, S - Donor Ligands Based on the P - N - P Motif)
Robert C. Haddon post-doc 2002-2006 UC Riverside
Herbert Walter Roesky post-doc 2006-2007 Universität Göttingen
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Publications

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Das A, Ahmed J, Rajendran NM, et al. (2020) A Bottleable Imidazole-Based Radical as a Single Electron Transfer Reagent. The Journal of Organic Chemistry
Chakraborty S, Das A, Ahmed J, et al. (2020) Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO functionalization. Chemical Communications (Cambridge, England)
Sau SC, Hota PK, Mandal SK, et al. (2020) Stable abnormal N-heterocyclic carbenes and their applications. Chemical Society Reviews
Gupta N, Ansari A, Dhoke GV, et al. (2020) Author Correction: Computationally designed antibody-drug conjugates self-assembled via affinity ligands. Nature Biomedical Engineering
Hota PK, Maji S, Ahmed J, et al. (2019) NHC-catalyzed silylative dehydration of primary amides to nitriles at room temperature. Chemical Communications (Cambridge, England)
Gupta N, Ansari A, Dhoke GV, et al. (2019) Computationally designed antibody-drug conjugates self-assembled via affinity ligands. Nature Biomedical Engineering
Ahmed J, Swain AK, Das A, et al. (2019) A K-arylacetylide complex for catalytic terminal alkyne functionalization using KOBu as a precatalyst. Chemical Communications (Cambridge, England)
Govindarajan R, Ahmed J, Swain AK, et al. (2019) Transition Metal-Free Catalytic Carboalkoxylation of Styrenes at Room Temperature. The Journal of Organic Chemistry
Das HS, Das S, Dey K, et al. (2019) Primary amides to amines or nitriles: a dual role by a single catalyst. Chemical Communications (Cambridge, England)
Bhunia M, Sahoo SR, Shaw BK, et al. (2019) Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction. Chemical Science. 10: 7433-7441
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