M. Sudershan Rao
Birla Institute of Technology and Science
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Publication
Featured researches published by M. Sudershan Rao.
Australian Journal of Chemistry | 2010
Anil Kumar; M. Sudershan Rao; V. Kameswara Rao
An efficient synthesis of 1-(benzothiazolylamino)methyl-2-naphthols has been developed in water by one-pot condensation of 2-naphthol, aldehydes and 2-aminobenzothiazole catalyzed by sodium dodecyl sulfate. Advantages of the methodology include a very short reaction time, excellent yields and catalytic use of the sodium dodecyl sulfate.
Journal of Sulfur Chemistry | 2009
Anil Kumar; Israr Ahmad; M. Sudershan Rao
Yb(OTf)3 in an ionic liquid [bmim][BF4] has been described as an efficient catalyst for the thia-Michael addition of thiols to α,β -unsaturated ketones to give β -aryl-β-mercapto ketones in 82–94% yield and the catalyst along with ionic liquid was recycled and reused.
Australian Journal of Chemistry | 2009
Anil Kumar; M. Sudershan Rao; Israr Ahmad; Bharti Khungar
Ytterbium triflate immobilized in the ionic liquid [bmim][BF4] catalyzes the three-component coupling of aromatic aldehydes, enolizable ketones, and acetonitrile in the presence of acetyl chloride at room temperature to afford β-acetamido ketones in good yields. The catalyst can be recovered and recycled for subsequent reactions without any appreciable loss of efficiency.
Green Chemistry Letters and Reviews | 2012
Anil Kumar; M. Sudershan Rao
Abstract An expeditious synthesis of 4H-chromenes has been achieved by three-component one-pot condensation of 1,3-diketone, aldehyde, and malononitrile using Ba(OTf)2 as catalyst in PEG-water at room temperature. Results from various reaction media and different metal triflates as catalysts show that choice of proper catalyst and the solvent system play a key role in the synthesis of 4H-chromene-3-carbonitrile derivatives. The catalyst can be recovered and reused at least five times without loss of activity. The application of an eco-friendly, noncorrosive, and reusable catalytic system with high isolated yield of the products makes this method advantageous.
Canadian Journal of Chemistry | 2008
Anil Kumar; Israr Ahmad; M. Sudershan Rao
Journal of Heterocyclic Chemistry | 2011
V. Kameswara Rao; M. Sudershan Rao; Anil Kumar
Archive | 2012
M. Sudershan Rao; Bhupender S. Chhikara; Rakesh Tiwari; Amir Nasrolahi Shirazi; Keykavous Parang; Anil Kumar
ChemInform | 2011
Anil Kumar; M. Sudershan Rao; Vibhor Mehta
Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry | 2009
Anil Kumar; Israr Ahmed; M. Sudershan Rao; Gautam Patel; Dalip Kumar
Archive | 2014
Bhupender S. Chhikara; M. Sudershan Rao; V. Kameshwara Rao