Saurabh Maity, PhD

About

Currently working in the CRO industry with expertise in organic synthesis, medicinal chemistry. I completed my Ph.D. from Indian Institute of Chemical Technology and subsequently received the National Postdoctoral Fellowship from the Science and Engineering Research Board.

My research experience includes transition metal-catalyzed C–H functionalization, total synthesis, and anticancer drug development through postdoctoral research at Indian Institute of Technology Kharagpur, India University of Göttingen, Germany and KU Leuven, Belgium.

Employment

• Jubilant Life Sciences (India) Team leader
  2022 - Present
• Avra Synthesis Private Limited Assistant Manager
  2016 - 2016

Education

• Indian Institute of Technology Kharagpur National Postdoctorate Fellow (SERB-NPDF)
  2016 - 2018
• Indian Institute of Chemical Technology Doctor of Philosophy (Ph. D.)
  2009 - 2015
• Vidyasagar University Master of Science (M. Sc.)
  2006 - 2008
• Midnapore College Bachelor of Science (B. Sc.)
  2003 - 2006

Projects & Funding

Projects & funding information is unavailable.

Publications (9)

• Transition Metal‐Catalysed Direct C−H Bond Functionalizations of 2‐Pyridone Beyond C3‐Selectivity
  Chemistry – An Asian Journal 2020 DOI: 10.1002/asia.202000506
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• Direct Pd(II)-Catalyzed Site-Selective C5-Arylation of 2-Pyridone Using Aryl Iodides
  Organic Letters 2018 DOI: 10.1021/acs.orglett.8b02112
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• Asymmetric Total Synthesis of the Putative Structure of Diplopyrone
  The Journal of Organic Chemistry 2017 DOI: 10.1021/acs.joc.7b00086
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• Gold(I)-Catalyzed Cyclization for the Synthesis of 8-Hydroxy-3- substituted Isocoumarins: Total Synthesis of Exserolide F
  Organic Letters 2017 DOI: 10.1021/acs.orglett.7b00673
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• Rhodium(III)-Catalyzed C6-Selective Arylation of 2-Pyridones and Related Heterocycles Using Quinone Diazides: Syntheses of Heteroarylated Phenols
  The Journal of Organic Chemistry 2017 DOI: 10.1021/acs.joc.7b00135
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• Regiocontrolled direct C4 and C2-methyl thiolation of indoles under rhodium-catalyzed mild conditions
  Chemical Communications 2017 DOI: 10.1039/c7cc07086a
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• Formal Total Synthesis of Brevisamide by Using a Tandem Isomerization/C-O and C-C Bond Formation Reaction
  European Journal of Organic Chemistry 2016 DOI: 10.1002/ejoc.201600142
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• Total synthesis of isocladosporin and 3- epi -isocladosporin
  Tetrahedron Letters 2016 DOI: 10.1016/j.tetlet.2015.11.060
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• An Efficient Formal Total Synthesis of Cladosporin
  European Journal of Organic Chemistry 2013 DOI: 10.1002/ejoc.201300053
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