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K. M. Muraleedharan

Researcher at Indian Institute of Technology Madras

Publications -  49
Citations -  802

K. M. Muraleedharan is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Artemisinin & Carboxylic acid. The author has an hindex of 12, co-authored 47 publications receiving 751 citations. Previous affiliations of K. M. Muraleedharan include University of Mississippi & Indian Institute of Chemical Technology.

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Journal ArticleDOI

One-step transformation of tricyclopentabenzene (trindane, C(15)H(18)) to bicyclo(10.3.0)pentadec-1(12)ene- 2,6,7,11-tetrone (C(15)H(18)O(4)) and its aldol product, 12-hydroxy-16-oxatetracyclo(10.3.1.0.(1,5)0(7,11))hexadec-7(11)ene-2,6-dione (C(15)H(18)O(4)).

Subramania Ranganathan, +4 more
- 14 Jul 2001 - 
TL;DR: This unique property of trindane offers opportunities for synthesis of complex natural products from this hydrocarbon that can be made in quantity by acid-catalyzed trimerization of cyclopentanone.
Journal ArticleDOI

Halo‐ and Selenolactonization: The Two Major Strategies for Cyclofunctionalization

Subramania Ranganathan, +3 more
- 31 Aug 2004 - 
Journal ArticleDOI

Benzisothiazolone Derivatives Exhibit Cytotoxicity in Hodgkin's Lymphoma Cells through NF-κB Inhibition and are Synergistic with Doxorubicin and Etoposide

Natarajan Nandakumar, +3 more
- 01 Jan 2020 - 
TL;DR: Benzisothiazolones bearing one or two electrophilic sulfur as part of the heterocyclic framework possess cytotoxicity through NF-ҡB, and especially BIT 1 and BIT 2 have in vitro anti-inflammatory and anti-cancer activity, with future potential therapeutic use.
Journal ArticleDOI

From helical supramolecular arrays to gel-forming networks: lattice restructuring and aggregation control in peptide-based sulfamides to integrate new functional attributes

Saripalli V. Raghava, +5 more
- 21 Mar 2018 - 
TL;DR: The assembly preference of a group of peptide-based sulfamides was modulated by making them part of an acid-amine two-component system to drive the tendency from crystallization to gelation, leading to Gelation of a number of solvents.
Journal Article

The preference profile in ruthenium tetroxide oxidations

Subramania Ranganathan, +3 more
- 01 Jan 1998 - 
TL;DR: The preference profile of Ru-VIII-generated in a catalytic cycle, maintained by periodate in carbon tetrachloride : acetonitrile : water has been examined from a practical vantage using tyrosine, phenylalanine and lysine as primary substrates as mentioned in this paper.