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Prof Sundarababu Baskaran

vidwan id: 42665
Male

Chair Professor, Department of Chemistry
Indian Institute of Technology Madras

Expertise

  • Organic Chemistry

Publications

Total Articles 60
Books 0
Proceedings 0

Publications

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Scopus

Citations 2081
h-index 25

CrossRef

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Citations 1742
h-index 23
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Professional Recognition

1991

Fellowship

Alexander von Humboldt, Germany
2013

Fellow of the Indian Academy of Sciences (FASc)

The Indian Academy of Sciences
2020

Fellow of the Indian National Science Academy (FNA)

Indian National Science Academy

Community & Membership

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Bio

Development of new strategies in Organic Synthesis, Enantioselective Synthesis, Synthesis of Biologically active Molecules/ Natural Products, Drug Design of Pharmaceutical Importance.

Personal Details

  • Male
  • Chair Professor , Indian Institute of Technology Madras
  • Indian Institute of Technology, Madras
Ph.D. (Chemistry)
Other Institute 1990
Chair Professor May 2018 – Present
Indian Institute of Technology Madras | Department of Chemistry
Professor May 2006 – Apr 2018
Indian Institute of Technology Madras | Department of Chemistry
Associate Professor May 2004 – Apr 2006
Indian Institute of Technology Madras | Department of Chemistry

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Co-Authors (5)

Ashok Kumar

Prof Ashok Kumar Mishra

Indian Institute of Technology Madras

Pradeep

Prof Pradeep Thalappil

Indian Institute of Technology Madras

Usharani

Prof Usharani Subuddhi

National Institute of Technology Rourkela

Sudhagar

Dr Sudhagar Selvaraju

National Institute of Pharmaceutical Education and Research (NIPER), Guwahati

Scholarly Work

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Synthesis of novel and structurally diverse iminosugar c-glycosides

University Indian Institute of Technology Madras
Year 2017

Diversity oriented one-pot synthesis of novel iminosugar c-glycosides

University Indian Institute of Technology Madras
Year 2016

Regioselective oxidative cleavage of benzylidene acetal: synthesis of functionalized uronic acid and sugar amino acid derivatives

University Indian Institute of Technology Madras
Year 2015

Chemo- and regioselective cleavage of benzylidene acetals: Stereoselective synthesis of functionalized chiral intermediates .

University Indian Institute of Technology Madras
Year 2009

Epoxide initiated domino olefin-Azide cyclization: Stereo- and enantioselective synthesis of azapolycycle ring systems .

University Indian Institute of Technology Madras
Year 2010

Development of new synthetic methods in low melting mixture and asymmetric organacatalytic aldol reaction.

University Indian Institute of Technology Madras
Year 2012

Stereo- and enantioselective synthesis of azatricyclic ring systems via domino semipinacol- schmidt reaction and mechanistic investigation on hooker oxidation.

University Indian Institute of Technology Madras
Year 2012

Stero-and enantioselective consrtuction of aza-quaternary center:application in the synthesis of natural products .

University Indian Institute of Technology Madras
Year 2012
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Scholarly Publications

Photophysical properties of Newkome-type dendrimers in aqueous medium

Open Access
Article
Authors: Mohanty S.K.;Subuddhi U.;Baskaran S.;Mishra A.K.

Regioselective oxidative cleavage of benzylidene acetals: synthesis of highly functionalized chiral intermediates

Open Access
Article

Synthesis of crispine A analogues via an intramolecular Schmidt reaction

Open Access
Article

Bathochromic shift of the fluorescence spectral maximum with increasing generation of dansyl labeled Newkome type dendrimers

Open Access
Article

An unusual solvent effect in the cuprate displacement reaction of indolizidin-5-yl-methyl p-toluenesulfonate: Stereoselective synthesis of indolizidine alkaloids

Open Access
Article

A facile, catalytic, and environmentally benign method for selective deprotection of teri-butyldimethylsilyl ether mediated by phosphomolybdic acid supported on silica gel

Open Access
Article

Regioselective cleavage of the bis-benzylidene acetal of D-mannitol under oxidative and reductive conditions: A new approach to C2-symmetric chiral ligands

Open Access
Article

1,3:4,6-Di-O-benzylidene-D-mannitol as a source for novel chiral intermediates through regioselective reductive cleavage

Open Access
Article