SDS Research Group

Independent Research:

13) Kingshuk Mahanty, Debabrata Maiti, Suman De Sarkar, "Regioselective C–H Sulfonylation of 2H-Indazoles by Electrosynthesis" J. Org. Chem. 2020, DOI: 10.1021/acs.joc.9b03330 (Joint 1st author)

 

 

 

 

 

 

 

 

12) Atreyee Halder, Debabrata Maiti, Suman De Sarkar, "Mechanochemical Synthesis of Functionalized Quinolines by Iodine Mediated Oxidative Annulation" Chemistry-An Asian Journal, 2020 DOI: 10.1002/asia.201901758 

 

 

 

 

 

 

 

11) Sanju Das,  Sushanta Kumar Parida, Tanumoy Mandal, Laxmikanta Sing,  Suman De Sarkar* and Sandip Murarka* "Organophotoredox Catalyzed Cascade Radical Annulation of 2-(Allyloxy)arylaldehydes with N-(acyloxy)phthalimides: Towards Alkylated Chroman-4-one derivatives" Chemistry-An Asian Journal, 2020 

 

 

 

 

 

 

 

 

10) S. Mallick, M. Baidya, K. Mahanty, D. Maiti, S. De Sarkar, "Electrochemical Chalcogenation of β,γ-Unsaturated Amides and Oximes to Corresponding Oxazolines and Isoxazolines" Adv. Synth. Catal. 2020 DOI: 10.1002/adsc.201901262. [Link]

9) D. Maiti, A. Halder, S. De Sarkar, "Base‐Promoted Aerobic Oxidation/Homolytic Aromatic Substitution Cascade toward the Synthesis of Phenanthridines" Adv. Synth. Catal. 2019 DOI: 10.1002/adsc.201900995. [Link] (Selected as VIP)

8) S. Das, S. Mallick, S. De Sarkar, "Cobalt-Catalyzed Sustainable Synthesis of Benzimidazoles by Redox-Economical Coupling of o-Nitroanilines and Alcohols" J. Org. Chem. 2019, 84, DOI: 10.1021/acs.joc.9b02090.[Link]

 

 

 

 

 

 

 

 

 

7) V. Arun, S. De Sarkar, "Recent Developments in the de Novo Synthesis of Heterocycles by First-Row Transition-Metal-Catalyzed Acceptorless Dehydrogenation" Cur. Org. Chem. 2019, 23, 1005.[Link]

6)    T. Mandal, S. Das, S. De Sarkar, "Nickel(II) Tetraphenylporphyrin as an Efficient Photocatalyst Featuring Visible Light Promoted Dual Redox Activities" Adv. Synth. Catal. 2019, 361, 3200.[Link]

5)     V. Arun, K. Mahanty, S. De Sarkar, "Nickel‐Catalyzed Dehydrogenative Couplings" Chem CatChem. 2019, 11, 2243.[Link] (Joint 1st author)

4)     M. Ghosh, S. De Sarkar, "meta‐ and para‐Selective C−H Functionalization using Transient Mediator and Noncovalent Template" Asian J. Org. Chem. 2018, 7, 1236.[Link]

3)     S. Das, D. Maiti, S. De Sarkar, "Synthesis of Polysubstituted Quinolines from α-2-Aminoaryl Alcohols Via Nickel-catalyzed Dehydrogenative Coupling" J. Org. Chem. 2018, 83, 2309.[Link]

2)     S. Dey, S. De Sarkar, "Synthetic Applications of Vinyl Ruthenium Carbene Derived from Diazoalkanes and Alkynes" Adv. Synth. Catal. 2017359, 2709. [Link]

1)     S. De Sarkar, "Remote C−H Functionalization by a Palladium-Catalyzed Transannular Approach" Angew. Chem., Int. Ed. 201655, 10558. [Link]

Doctoral and Postdoctoral Research:

 

17)    J. Li, K. Korvorapun, S. De Sarkar, T. Rogge, D. J. Burns, S. Warratz, L. Ackermann, Nature Commun. 2017, 8, 15430. [Link] (Joint 1st author)

16)    S. De Sarkar, N. Y. P. Kumar and L. Ackermann, Chem. Eur. J. 201723, 84. [Link]

15)    S. De Sarkar, J. F. Blom, Y. Bethuel, F. Jüttner, K. Gademann, Helv. Chim. Acta. 2016, 99, 760. [Link]

14)    J. Li, S. De Sarkar and L. Ackermann, Top. Organomet. Chem. 201655, 217. [Link]

 

13)    J. Li, S. Warratz, D. Zell, S. De Sarkar, E. E. Ishikawa, L. Ackermann, J. Am. Chem. Soc. 2015, 137, 13894. [Link]

 

12)    S. De Sarkar and L. Ackermann, Chem. Eur. J. 201420, 13932. [Link]

(Most Accessed Article 09-2014 to 08-2015 and Selected for ChemInform Abstract 2015 by the Editors)

 

11)    S. De Sarkar, W. Liu, S. I. Kozhushkov and L. Ackermann, Adv. Synth. Catal. 2014356, 1461. [Link]

(>174 Citations)

10)    R. C. Samanta, S. De Sarkar, R. Fröhlich, S. Grimme and A. Studer, Chem. Sci. 20134, 2177. [Link]

 

9)   S. De Sarkar, A. Biswas, R. C. Samanta and A. Studer, Chem. Eur. J. 201219, 4664. [Link]

(>114 Citations and selected for ChemInform Abstract 2013 by the Editors)

 

8)   A. Biswas, S. De Sarkar, L. Tebben and A. Studer, Chem. Commun. 201248, 5190. [Link]

 

7)   R. C. Samanta, B. Maji, S. De Sarkar, K. Bergander, R. Fröhlich, C. M.-Lichtenfeld, H. Mayr and A. Studer, Angew. Chem., Int. Ed. 201251, 5234. [Link]

 

6)    A. Biswas, S. De Sarkar and A. Studer, Org. Lett. 201113, 4966. [Link]

(Selected for ChemInform Abstract 2012 by the editors)

 

5)    S. De Sarkar, A. Biswas, C. H. Song and A. Studer, Synthesis 201112, 1974. [Link]

 

4)   S. De Sarkar and A. Studer, Angew. Chem., Int. Ed. 201049, 9266. [Link]

(>143 Citations and highlighted in Synfacts 2011, 96)

 

3)   S. De Sarkar and A. Studer, Org. Lett. 201012, 1992. [Link]

(>133 Citations and selected for ChemInform Abstract 2010 by the editors)

 

2)   S. De Sakar, S. Grimme and A. Studer, J. Am. Chem. Soc. 2010132, 1190. [Link]

(>185 Citations and highlighted in Synfacts 2010, 359)

 

1)    J. Guin, S. De Sarkar, S. Grimme and A. Studer, Angew. Chem., Int. Ed. 200847, 8727. [Link]

(>134 Citations and highlighted in Synfacts 2009, 26)

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