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Study of cavity size and nature of bridging units on recognition of nucleotides by cyclophanes

Study of cavity size and nature of bridging units on recognition of nucleotides by cyclophanes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Neelakandan, PP; Nandajan, PC; Subymol, B; Ramaiah, D
  • Volume :
  • Year : 2011
A novel NHC-catalyzed transformation of 2H-chromene-3-carboxaldehydes to 3-methyl-2H-chromen-2-ones

A novel NHC-catalyzed transformation of 2H-chromene-3-carboxaldehydes to 3-methyl-2H-chromen-2-ones

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Sinu, CR; Rejithamol, R; Lakshmi, KCS; Suresh, E
  • Volume :
  • Year : 2011
A facile four component protocol for the synthesis of dihydropyridine derivatives

A facile four component protocol for the synthesis of dihydropyridine derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Jose, A; Lakshmi, KCS; Rajan, R; Suresh, E
  • Volume :
  • Year : 2012
Mechanism of epoxide hydrolysis in microsolvated nucleotide bases adenine, guanine and cytosine: A DFT study

Mechanism of epoxide hydrolysis in microsolvated nucleotide bases adenine, guanine and cytosine: A DFT study

  • --- Research Area : Environmental Technology Division (ETD)
  • Author : Vijayalakshmi, KP; Mohan, N; Ajitha, MJ; Suresh, CH
  • Volume :
  • Year : 2011
4,4,9,9-Tetraphenyl pyrroloindolizine: a structural analogue of calix[2] pyrrole

4,4,9,9-Tetraphenyl pyrroloindolizine: a structural analogue of calix[2] pyrrole

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Sreedevi, KCG; Thomas, AP; Ramakrishnan, S; Salini, PS; Holaday, MGD; Reddy, MLP; Srinivasan, A
  • Volume :
  • Year : 2012
BF3 center dot Et2O mediated one-step synthesis of N-substituted-1,2-dihydropyridines, indenopyridines and 5,6-dihydroisoquinolines

BF3 center dot Et2O mediated one-step synthesis of N-substituted-1,2-dihydropyridines, indenopyridines and 5,6-dihydroisoquinolines

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Salfeena, CTF; Ashitha, KT; Sasidhar, BS
  • Volume :
  • Year : 2016
Phosphine-mediated reaction of 3-methyl allenoate and isatins: a protocol for the synthesis of spirofuran oxindoles

Phosphine-mediated reaction of 3-methyl allenoate and isatins: a protocol for the synthesis of spirofuran oxindoles

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Jose, A; Jayakrishnan, AJ; Lakshmi, KCS; Varughese, S; Nair, V
  • Volume :
  • Year : 2015
A lysosome-targeted drug delivery system based on sorbitol backbone towards efficient cancer therapy

A lysosome-targeted drug delivery system based on sorbitol backbone towards efficient cancer therapy

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Maniganda, S; Sankar, V; Nair, JB; Raghu, KG; Maiti, KK
  • Volume :
  • Year : 2014
Trapping the Lewis acid generated transient species from pentafulvene derived diazanorbornenes with ortho-functionalized aryl iodides and aliphatic alcohols

Trapping the Lewis acid generated transient species from pentafulvene derived diazanorbornenes with ortho-functionalized aryl iodides and aliphatic alcohols

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Chand, SS; Saranya, S; Preethanuj, P; Dhanya, BP; Jijy, E; Prakash, P; Sasidhar, BS; Szymoniak, J; Santhini, PV; Radhakrishnan, KV
  • Volume :
  • Year : 2014
A metal-free one-pot cascade synthesis of highly functionalized biaryl-2-carbaldehydes

A metal-free one-pot cascade synthesis of highly functionalized biaryl-2-carbaldehydes

  • --- Research Area : Agroprocessing & Technology Division (APTD)
  • Author : Challa, C; Vellekkatt, J; Ravindran, J; Lankalapalli, RS
  • Volume :
  • Year : 2014