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Cu(II)-mediated generation of triarylamine radical cations and their dimerization. An easy route to tetraarylbenzidines

Cu(II)-mediated generation of triarylamine radical cations and their dimerization. An easy route to tetraarylbenzidines

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Sreenath, K; Suneesh, CV; Kumar, VKR; Gopidas, KR
  • Volume :
  • Year : 2008
Fluorescence Ratiometric Selective Recognition of Cu2+ Ions by Dansyl-Naphthalimide Dyads

Fluorescence Ratiometric Selective Recognition of Cu2+ Ions by Dansyl-Naphthalimide Dyads

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Jisha, VS; Thomas, AJ; Ramaiah, D
  • Volume :
  • Year : 2009
Assessment of Stereoelectronic Factors That Influence the CO2 Fixation Ability of N-Heterocyclic Carbenes: A DFT Study

Assessment of Stereoelectronic Factors That Influence the CO2 Fixation Ability of N-Heterocyclic Carbenes: A DFT Study

  • --- Research Area : Environmental Technology Division (ETD)
  • Author : Ajitha, MJ; Suresh, CH
  • Volume :
  • Year : 2012
DFT Prediction of Multitopic N-Heterocyclic Carbenes Using Clar's Aromatic Sextet Theory

DFT Prediction of Multitopic N-Heterocyclic Carbenes Using Clar's Aromatic Sextet Theory

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Suresh, CH; Ajitha, MJ
  • Volume :
  • Year : 2013
Synthesis of beta-C-Galactosyl Ceramide and Its New Aza Variant via the Horner-Wadsworth-Emmons Reaction

Synthesis of beta-C-Galactosyl Ceramide and Its New Aza Variant via the Horner-Wadsworth-Emmons Reaction

  • --- Research Area : Agroprocessing & Technology Division (APTD)
  • Author : Gorantla, JN; Lankalapalli, RS
  • Volume :
  • Year : 2014
Narrow-Rim Functionalization of Calix[4]arene through Ugi-4CR: Synthesis of a Series of Calix[4]arene Peptoids

Narrow-Rim Functionalization of Calix[4]arene through Ugi-4CR: Synthesis of a Series of Calix[4]arene Peptoids

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Savithri, A; Thulasi, S; Varma, RL
  • Volume :
  • Year : 2014
p-TSA/Base-Promoted Propargylation/Cyclization of beta-Ketothioamides for the Regioselective Synthesis of Highly Substituted (Hydro)thiophenes

p-TSA/Base-Promoted Propargylation/Cyclization of beta-Ketothioamides for the Regioselective Synthesis of Highly Substituted (Hydro)thiophenes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nandi, GC; Singh, MS
  • Volume :
  • Year : 2016
Catalyst-Controlled Straightforward Synthesis of Highly Substituted Pyrroles/Furans via Propargylation/Cycloisomerization of alpha-Oxoketene-N,S-acetals

Catalyst-Controlled Straightforward Synthesis of Highly Substituted Pyrroles/Furans via Propargylation/Cycloisomerization of alpha-Oxoketene-N,S-acetals

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nandi, GC; Soumini, K
  • Volume :
  • Year : 2016
One-Pot MCR-Oxidation Approach toward Indole-Fused Heteroacenes

One-Pot MCR-Oxidation Approach toward Indole-Fused Heteroacenes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Santhini, PV; Krishnan, RA; Babu, SA; Simethy, BS; Das, G; Praveen, VK; Varughese, S; John, J
  • Volume :
  • Year : 2017
An N-heterocyclic carbene-catalyzed [8+3] annulation of tropone and enals via homoenolate

An N-heterocyclic carbene-catalyzed [8+3] annulation of tropone and enals via homoenolate

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Poonoth, M; Vellalath, S; Suresh, E; Thirumalai, R
  • Volume :
  • Year : 2006