IIEST, Shibpur

Indian Institute of Engineering Science and Technology, Shibpur

(Formerly Bengal Engineering and Science University, Shibpur)

Empowering the nation since 1856

आई आई ई एस टि, शिवपुर

भारतीय अभियांत्रिकी विज्ञान एवं प्रौद्योगिकी संस्थान, शिवपुर

(पूर्व में बंगाल इंजीनियरिंग एंड साइंस यूनिवर्सिटी)

१८५६ से देश को सशक्त बनाना

  1. T. K. Sarkar and B. K. Ghorai, " Silicon-directed Bamford Stevens Reactions of β- Trimethylsilyl N-Aziridinylimines", J. Chem. Soc., Chem. Commun., 1992, 1184–1185. (20)
  1. T. K. Sarkar, S. K. Ghosh, P. S. V. Subba Rao, and B. K. Ghorai, "An ‘Anomalous’ Ozonolysis of an Olefin: Isolation and Crystal Structure of Methyl (4aRS, 8RS, 8aRS)-Decahydro-2, 5-dioxo-quinoline-8-carboxylate", J. Chem. Research(s), 1992, 394–395 and J. Chem. Research(M), 1992, 3001–3014.
  1. T. K. Sarkar, B. K. Ghorai, S. K. Nandy and B. Mukherjee, "Intramolecular Alder Ene Reactions of activated 1,6-Dienes: Stereochemical Control over three Contiguous Stereogenic Centers", Tetrahedron Lett., 1994, 35, 6903–6906.  (Google Scholar: 11; not showing in Scopus)
  1. T. K. Sarkar, B. K. Ghorai, and A. Banerji, "Intramolecular Alder Ene Approach to Stereochemical Control over three Contiguous Stereogenic Centers: Synthesis of (±)- Methyl Cucubate and (±)-Methyl Epijasmonate", Tetrahedron Lett., 1994, 35, 6907–6908. (17)
  1. T. K. Sarkar, S. K. Nandy, B. K. Ghorai and B. Mukherjee, "Lithium Perchlorate Dispersed on Silica Gel, a Mild and Efficient Catalyst for Intramolecular Ene Reactions of Activated 1,6- and 1,7- Dienes", Synlett, 1996, 97–99. (10)
  1. T. K. Sarkar, B. K. Ghorai, S. K. Das, P. Gangopadhyay and P. S. V. Subba Rao, "Siliocon as Controlling Element for Regioselective Ene Reaction of DEAD with (Homo)Allylic Silanes. Application to the Synthesis of Cyclic 1,2-Dinitrogen Compounds", Tetrahedron Lett., 1996, 37, 6607–6610. (13)
  1. T. K. Sarkar, B. K. Ghorai, S. K. Nandy, B. Mukherjee and A. Banerji, "Stereochemical Control over three Contiguous Stereogenic Center in the Intramolecular Ene Reaction of activated 1,6-Dienes. Application to the Synthesis of (±)- Methyl Cucubate and (±)-Methyl Epijasmonate", J. Org. Chem., 1997, 62, 6006–6011. (15)
  1. T. K. Sarkar, P. Gangopadhyay, B. K. Ghorai, S. K. Nandy and J-M. Fang, "Cyclopentanoid Allylsilane in Synthesis: A Facile Construction of the 5-8 Carbon Frame work of Asteriscanolide", Tetrahedron Lett., 1998, 39, 8365–8366. (16)
  1. T. K. Sarkar and B. K. Ghorai, "Methyl Epijasmonate: Historical Perspective and Total Synthesis", J. Indian Chem. Soc., 1999, 76, 693–706. (16)
  1. B. K. Ghorai, J. W. Herndon and Y.–F. Lam, "One-Step Convergent Synthesis of the Steroid Ring System via the Coupling of γ, d-Unsaturated Fischer Carbene Complexes with o-Ethynylbenzaldehyde", Organic Lett., 2001, 3, 3535–3538. (36)
  1. B. K. Ghorai, S. Menon, D. L. Johnson and J. W. Herndon, “Inversion of the Direction of Stereoinduction in the Coupling of Chiral g, d-Unsaturated Fischer Carbene Complexes with o-Ethynylbenzaldehyde”, Organic Lett., 2002, 4, 2121–2124. (22)
  1. B. K. Ghorai and J. W. Herndon, “Coupling of Fischer Carbene Complexes with o-Alkynylbenzamides”, Organometallics, 2003, 22, 3951–3957. (21)
  1. B. K. Ghorai, D. Jiang and J. W. Herndon, “Novel Synthesis of Isoquinolines Using Isobenzofuran- Nitriles Diels Alder Reactions”, Organic Lett., 2003, 5, 4261–4263. (33)
  1. B. K. Ghorai, S. Duan, D. Jiang and J. W. Herndon, Coupling of β-Cyanocarbene-Chromium Complexes with 2-Alkynylbenzoyl Derivatives: A [5+5]-Cycloaddition Approach to Phenanthridines”, Synthesis, 2006, (21), 3661–3669. (17)
  1. G. P. Jana and B. K. Ghorai, “Tandem furo[3,4-b]pyridine formation-Diels Alder reaction: an approach to the synthesis of nitrogen containing heterocyclic analogues of 1-arylnaphthalene lignans”, Tetrahedron, 2007, 63, 12015–12025. (17)
  1. G. P. Jana and B. K. Ghorai, “Tandem Generation and Trapping of Furo[3,4-c]isoquinoline Intermediates Leading to the Synthesis of Phenanthridine Ring Systems”, Lett. Org. Chem., 2009, 6, 372–376. (7)
  1. S. Mukherjee, G. P. Jana and B. K. Ghorai, “Synthesis of isoquinolines through the coupling of Fischer carbene complexes with o-alkynylpyridine carbonyl derivatives”, J. Organomet. Chem., 2009, 694, 4100–4106. (11)
  1. D. Jana and B. K. Ghorai, “Design, Synthesis and Optical Response of Pyridine-Cored V-Shaped Stilbenoid Dendrimers”, Lett. Org. Chem., 2010, 7, 203–207. (2)
  1. S. Mukherjee and B. K. Ghorai, “Metalation of 2,4-dialkoxy-5-bromopyrimidine and formylation with dimethylformamide: Isolation of unexpectedly formed 2,6-dialkoxy-5-dimethylaminopyrimidine-4-carboxaldehyde”, Synth. Commun., 2010, 40, 1939–1943.
  1. P. Roy and B. K. Ghorai, “One-pot three-component synthesis of quinoxaline and phenazine ring systems using Fischer carbene complexes”, Beilstein J. Org. Chem., 2010, 6, No. 52. doi:10.3762/bjoc.6.52 (17)
  1. G. P. Jana, S. Mukherjee and B. K. Ghorai, “Multicomponent approach for the synthesis of phenanthridine and acridine ring systems via the coupling of Fischer carbene complexes with heteroaromatic o-alkynyl Carbonyl derivatives”, Synthesis, 2010, 31793189. (14)
  1. P. Roy, D. Jana and B. K. Ghorai, “Synthesis and Photophysical Properties of Stilbenoid Dendrimers via Heck Reaction on a Tetraphenylethylene Core”, Bull. Chem. Soc. Jpn., 2010, 83, 1269–1271. (4)
  1. P. J. P. Yadav, A. K. Patra, P. U. Sastry, B. K. Ghorai and P. Maiti, “Solvent Retention, Thermodynamics, Rheology and Small Angle X-ray Scattering Studies on Thermoreversible Poly(vinylidene fluoride) Gels” J. Phys. Chem. B, 2010, 114, 11420–11429. (6)
  1. P. Roy and B. K. Ghorai, “One-pot synthesis of furo[2,3-h]quinoline and furo[2,3-h]isoquinoline derivatives using Fischer carbene complex”, Tetrahedron Lett. 2011, 52, 251–253. (10)
  1. S. Mukherjee, P. Roy and B. K. Ghorai, “One-pot three-component synthesis of quinoxaline, quinazoline and phenazine ring systems using Fischer carbene complexes”, Synthesis, 2011, 14191426. (11)
  1. P. J. P. Yadav, B. Maiti, B. K. Ghorai, P. U. Sastry, A. K. Patra, V. K. Aswal  and P. Maiti, “Thermoreversible Gelation of Poly(vinylidene fluoride-co-chlorotrifluoroethylene): Structure, Morphology, Thermodynamics, and Theoretical Prediction”, Macromolecules, 2011, 44, 30293038. (6)
  1. P. Roy and B. K. Ghorai, “Annulation of furan-bridged 10-membered rings on N-heterocycles through [8+2] cycloaddition of dienylazaisobenzofurans and dimethyl acetylenedicarboxylate”, Tetrahedron Lett. 2011, 52, 5668–5671. (9)
  1. D. Jana and B. K. Ghorai, “Synthesis and photophysical properties of tetraphenylethylene-based conjugated dendrimers with triphenylamine core”, Tetrahedron Lett. 2012, 53, 196–199. (15)
  1. P. Roy and B. K. Ghorai, “One-pot synthesis of pyrano[4,3-b]quinolinones from 2-alkynyl-3-formylquinolines via oxidative 6-endo-dig ring closure”, Tetrahedron Lett. 2012, 53, 235–238. (7)
  1. D. Jana and B. K. Ghorai, “Synthesis and fluorescence behaviour of star-shaped pyridine and benzene cored stilbenoid compounds” J. Indian Chem. Soc. 2012, 89, 405–410.
  1. D. Jana and B. K. Ghorai, “Triphenylpyridine-based star-shaped π-conjugated oligomers with triphenylamine core: Synthesis and photophysical properties”, Tetrahedron Lett. 2012, 53, 1798–1801. (9)
  1. D. Jana and B. K. Ghorai, “Pyridine–cored V–shaped π–conjugated oligomers: synthesis and optical properties”, Tetrahedron 2012, 68, 7309–7316. (15)
  1. D. Jana and B. K. Ghorai, “Synthesis and aggregation-induced emission properties of tetraphenylethylene–based oligomers containing triphenylethylene moiety”, Tetrahedron Lett. 2012, 53, 6838–6842. (29)
  1. P. Roy, P. Mitra and B. K. Ghorai, “Synthesis of azahomosteroid ring system through intramolecular [4+2] cycloaddition of in situ generated azaisobenzofuran intermediates”, Tetrahedron Lett. 2013, 54, 1440–1443. (7)
  2. D. Jana, S. Boxi and B. K. Ghorai, “Synthesis of gem-tetraphenylethylene oligomers utilizing Suzuki reaction and their aggregation properties”, Dyes and Pigments 2013, 99, 740–747. (10)
  3. D. Jana and B. K. Ghorai, “Hexaphenylbenzene end-capped tri(p-phenylenevinylene): Synthesis and properties”, Tetrahedron Lett. 2014, 55, 5203–5206. (3)
  4. D. Jana and B. K. Ghorai, “Side substituent dependence of photophysical properties of 9-arylanthracene based π-conjugates”, Bull. Chem. Soc. Jpn., 2015, 88, 89–96. (doi: 10.1246/bcsj.20140178).
  5. D. Jana, S. Boxi, P. P. Parui and B. K. Ghorai, “Planar-Rotor architecture based pyrene-vinyl-tetraphenylethylene conjugated systems: photophysical properties and aggregation behavior”, Org. Biomol. Chem., 2015, 13, 10663–10674.
  6.  N. Pradhan, D. Jana, B. K. Ghorai and  N. Jana, “Detection and Monitoring of Amyloid Fibrillation Using Fluorescence ‘Switch-On’ Probe” ACS Appl. Mater. Interfaces, 2015, 7, 25813−25820. (DOI: 10.1021/acsami.5b07751) (19)
  7. Kuheli Mandal, Debabrata Jana, Binay K. Ghorai, and Nikhil R. Jana, “Fluorescent Imaging Probe from Nanoparticle Made of AIE Molecule” J. Phys. Chem. C, 2016, 120, 5196−5206. (19)
  8. Kuheli Mandal, Debabrata Jana, Binay K. Ghorai, and Nikhil R. Jana, “Functionalized chitosan with self-assembly induced and subcellular localization-dependent fluorescence ‘switch on’ property” New J. Chem, 2018, 42, 5774-5784. (1)
  9. S. Biswas, D. Jana, G. Kumar, S. Maji, P. Kundu, U. Ghorai, R. Giri, B. Das, N. Chattopadhyay, B. K; Ghorai, S. Acharya, “Supramolecular Aggregates of Tetraphenylethene Cored AIEgen towards  Mechanoluminescent and Electroluminescent Devices" ACS Appl. Mater. Interfaces, 2018, 10, 14966–14977. (3)
  10. S. Boxi, D. Jana, P. P. Parui and B. K. Ghorai, “Dibenzo[a,c]phenazine based donor-acceptor (D-A) tetra branched molecules: Fine tuning of optical properties”, Chemistry Select., 2018, 3, 6953-6959.
  11. S. Boxi, D. Jana and B. K. Ghorai, “Synthesis and Optical Properties of Bipolar Quinoxaline-Triphenylamine Based Stilbene”, Optical Materials, 2019, https://doi.org/10.1016/j.omx.2019.100013.
  12. Kuheli Mandal, Debabrata Jana, Binay K. Ghorai, Nikhil Jana, “AIEgen-Conjugated Magnetic Nanoparticles as Magnetic-Fluorescent Bioimaging Probes" ACS Appl. Nano Mater., 2019, 2, 3292-3299.

Scopus citation as on 21.02.2019 is 491. [H index 15, i10 index=24]