68. “Solvent-Free Synthesis of Pillar[6]arenes” S Santra, DS Kopchuk, IS Kovalev, GV Zyryanov, Green Chem. 2016,18, 423-426
67. “Copper(I)-Catalyzed Oxidative Coupling between 2–Aminobenzothiazole and Terminal Alkyne: Formation of Benzothiazine” S. Mitra, A. Chakraborty, S. Mishra, A. Majee, A. Hajra Org. Lett. 2014, 16, 5652-5655
66. “Microwave-Assisted Three-Component ‘‘Catalyst and Solvent-Free’’ Green Protocol: A Highly Efficient and Clean One-Pot Synthesis of Tetrahydrobenzo[b]pyrans”. S. Santra, M. Rahman, A. Roy, A. Majee, A. Hajra Res. Chem. Intermed. 2014, (DOI.org/10.1155/2014/851924)
65. “Iron(III)-Catalyzed Three-Component Domino Strategy for the Synthesis of Imidazo[1,2-a]pyridines”. S. Santra, S. Mitra, A. K. Bagdi, A. Majee, A. Hajra Tetrahedron Letters 2014, 55, 5151-55
64*. “Solvent-free silica-promoted multicomponent condensation: Synthesis of highly
functionalized piperidines”. S. Das, A. K. Bagdi, S. Santra, A. Majee, A. Hajra,
Research on Chemical Intermediates 2014, (in press, DOI 10.1007/s11164-014-1774-7)
63. “Copper(II)-catalyzed aerobic oxidative coupling between chalcone and 2-aminopyridine via C-H Amination: An expedient synthesis of 3-aroylimidazo[1,2-a]pyridines”. K. Monir, A. K. Bagdi, S. Mishra, A. Majee, A. Hajra, Adv. Synth. Catal. 2014, 356, 1105.
62. “Nano indium oxide: An efficient catalyst for one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones with a greener prospect”. S. Santra, M. Rahman, A. Roy, A. Majee, A. Hajra, Catal. Commun. 2014, 49, 52.
61*. “Phenyliodine (III) diacetate (PIDA) mediated synthesis of aromatic azo compounds through oxidative dehydrogenative coupling of anilines: Scope and mechanism”. K. Monir, M. Ghosh, S. Mishra, A. Majee, A. Hajra, Eur. J. Org. Chem. 2014, 1096.
60*. “Catalytic application of task specific ionic liquid on the synthesis of benzoquinazolinone derivatives by a multicomponent reaction”. M. Rahman, A. Sarkar, M. Ghosh, A. Majee, A. Hajra, Tetrahedron Lett. 2014, 55, 235.
59*. “Organocatalysis by aprotic imidazolium zwitterion: A dramatic anion–cation cooperative effect on azide-nitrile cycloaddition” A. Hajra, A. Majee, M. Rahman, A. Roy and M. Ghosh , RSC Adv., 2014, 4, 6116,
58.* “An improved procedure of Miyashita protocol for the preparation of ureidomethylene derivatives of 1,3-dicarbonyl compounds” A. Majee, S. K. Kundu, S. Santra and A. Hajra. Ind. J. Chem B 2014 53B 124
57*. “Metal nanoparticles in “on-water” organic synthesis: one-pot nano CuO catalyzed synthesis of isoindolo[2,1-a]quinazolines” S. Santra, A. K. Bagdi, A. Majee and A. Hajra RSC Adv., 2013, 3, 24931-24935
56. “Synthesis of polysubstituted quinolines via copper(II)-catalyzed annulation of 2-aminoaryl ketones with alkynoates” A. K. Bagdi, S. Santra, M. Rahman, A. Majee and A. Hajra RSC Adv., 2013, 3, 24034-24037
55. “Synthesis, structure and catalytic aspects of the palladium(II) complex [PdLCl] (where LH = 2-formyl-4-methyl-6-N-ethylpiperidineiminomethylphenol).” D. Das, P. Maiti, A. K. Bagdi, T. Ghosh, T. Chattopadhay, S. Das, A. Hajra, A. Majee and E. Zangrand. Indian Journal of Chemistry 2013, 52A, 863-867
54.* “Nano indium oxide catalyzed tandem cyclization of amidine with nitroolefin.” S. Mitra, A. K. Bagdi, A. Majee, A. Hajra Tetrahedron Letters, 2013, 54, 4982-4985.
53. “Regioselective synthesis of pyrano[3,2-c]coumarins via Cu(II)-catalyzed tandem reaction.” A. K. Bagdi, A. Majee, A. Hajra, Tetrahedron Letters, 2013, 54, 3892-3895.
52. “Copper-catalyzed synthesis of imidazo[1,2-a]pyridines through tandem imine formation-oxidative cyclization under ambient air: One-step synthesis of zolimidine on a gram-scale.” A. K. Bagdi, M. Rahman, S. Santra, A. Majee, A. Hajra, Adv. Synth. Catal. 2013, 355, 1741-1747.
51. “Iron(III)-Catalyzed Cascade Reaction between Nitroolefins and 2-Aminopyridines: Synthesis of Imidazo[1,2-a] pyridines and Easy Access towards Zolimidine.” S. Santra, A. K. Bagdi, A. Majee, and A. Hajra, Adv. Synth. Catal. 2013, 355, 1065
50.* “Dialkyl phosphite as a highly selective mono- N-alkylating agent using indium triflate under microwave irradiation.” S. K. Kundu, K. Mitra and A. Majee . RSC Adv., 2013, 3, 8649–8651
49.* “A simple and efficient approach for sulfonation of indoles catalyzed by CuI”
M. Rahman, M. Ghosh, A. Hajra and A. Majee Journal of Sulpher Chemistry 2013, 34, 342
48. “Zwitterionic-Type Molten Salt-Catalyzed Multi-Component Reactions: One-Pot Synthesis of Substituted Imidazoles under Solvent-Free Conditions.” M. Rahman, A. K. Bagdi, D. Kundu, A. Majee and A. Hajra Journal of Heterocyclic Chemistry 2012, 49, 1224-1228.
47.* “A mild and efficient Synthesis of 1,5- benzo-diazepine derivatives catalysis by acidic ionic liquid in solvent free condition.” A. Roy, A. Majee and A. Hajra Journal of Indian chemical Society 2012, 89, 963-965.
46.* “Combination of NH2OH.HCl and NaIO4: a new and mild oxidizing agent for selective oxidation of alcohols to carbonyl compounds.” A. Majee, S. K. Kundu, S. Santra, A. Hajra Tetrahedron Lett., 2012, 53, 4433-4435.
45.* “An efficient and alternative approach for preparation of O-benzoylozimes using benzoyl peroxide.” S. K. Kundu, M. Rahman, P. Dhara, A. Hajra and A. Majee Synth. Commun. 2012, 42, 1848-1854
44.* “Nano indium oxide: an efficient catalyst for the synthesis of 1,2-disubstituted benzimidazoles in aqueous media.” S. Santra, A. Majee, A. Hajra Tetrahedron Lett., 2012, 53, 1974-1977
43. “One-Pot Multicomponent Synthesis of Polyhydroquinolines under Catalyst and Solvent-Free Conditions.” S. Das, S. Santra, A. Roy, S. Urinda, A. Majee, A. Hajra Green Chem. Lett. Rev. 2012, 5, 97-100.
42. “A Convenient Synthesis of Coumarins using Reusable Ionic Liquid as Catalyst.” S. Das, A. Majee and A. Hajra Green Chem. Lett. Rev. 2011, 4, 349.
41. “Nano indium oxide catalyzed efficient synthesis of propargylamines via C_H and C_Cl bond activations.” M. Rahman, A. K. Bagdi, A. Majee and A. Hajra Tetrahedron Letters 2011, 52, 4437.
40.* “Task-Specific Ionic Liquid-Catalyzed Efficient Couplings of Indoles with 1,3-Dicarbonyl Compounds: An Efficient Synthesis of 3-Alkenylated Indoles.” S. Santra, A. Majee and A. Hajra Tetrahedron Letters 2011, 52, 3825.
39. “Zwitterionic-type molten salt: A mild and efficient organocatalyst for the synthesis of 3-aminoalkylated indoles via three-component coupling reaction.” D. Kundu, A. K. Bagdi, A. Majee, and A. Hajra Synlett 2011, 1165.
38. “Indium triflate-catalyzed coupling between nitroalkene and phenol/naphthol: a simple and direct synthesis of benzofuran and naphthofuran via cyclization reaction.” D. Kundu, A. Majee and A. Hajra Chemistry-An Asian Journal, 2011, 6, 406.
37. “Task-specific ionic liquid catalyzed efficient microwave assisted synthesis of 12-alkyl or aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-ones under solvent-free conditions.” D. Kundu, A. Majee, and A. Hajra, Green Chem. Lett. Rev. 2011, 4, 205
36. “Microwave-assisted Bronsted acidic ionic liquid promoted one-pot synthesis of heterobicyclic dihydropyrimidinones.” M. Rahman, A. Majee, A. Hajra, J. Het. Chem., 2010, 47, 1230-1233.
35.* “Manganese (II) Chloride-Catalyzed Conjugated Addition of Amines to
Electron Deficient Alkenes in Methanol-Water Medium” A. Roy, D. Kundu, S. K. Kundu, A. Majee and A. Hajra The Open Catalysis Journal, 2010, 3, 34-39
34.* “Formylation without Catalyst and solvent at 80 oC” M. Rahman, D. Kundu, A.Hajra, A. Majee Terahedron Lett. 2010, 51, 2896-2898 (correction 2010, 51 4585-4586)
33. “Zwitterionic-type molten salt: an efficient mild catalyst for synthesis of 2-amidoalkyl and 2-carbamatoalkyl naphthols.” D. Kundu, A. Majee, A. Hajra Catal. Commun. 2010, 11, 1157.
32. “Task-specific ionic-liquid-catalyzed efficient synthesis of indole derivatives under solvent free condition” S. Das, M. Rahman D. Kundu, A. Majee, A. Hajra Can. J. Chem. 2010, 88, 150.
31.* “TBATB – a useful catalyst for synthesis of bis (indolyl) methane derivatives at room temperature” S. K.Kundu, S. Islam A. Majee Russ. J. Org. Chem 2010, 46, 126-128
30.* “An Efficient One-Pot Synthesis of Naphthoxazinones by a Three-Component Coupling of Naphthol, Aldehydes, and Urea Catalyzed by Zinc Triflate” D. Kundu, A. Majee, A. Hajra J. Het. Chem.. 2009, 46, 1019-1022.
29.* “Indium triflate-catalyzed one-pot synthesis of 14-alkyl or aryl-14H-dibenzo[a,j] xanthenes in water” S. Urinda, D. Kundu, A. Majee, A. Hajra J. Het. atom.. 2009, 20, 232-234.
28.* “A Convenient Synthesis of 1,5- benzothiazepine with Microwave Irradiation under Solvent or Catalyst free condition” M. Rahman, A. Roy, A. Majee A. Hajra J. Chem. Res. 2009, 178-179
27. “Zwitterionic-type molten salt-catalyzed syn-selective aza-Henry reaction:
solvent-free one-pot synthesis of b-nitroamines” D. Kundu, R. K. Debnath, A. Majee, A. Hajra Terahedron Lett. 2009, 50, 6998-.
26.* “Indium triflate-catalyzed one-pot synthesis of 1-subtituted-1H-1,2,3,4-tetrazoles under solvent-free conditions” D. Kundu, A. Majee, A. Hajra Terahedron Lett. 2009, 50, 2668-2670.
25.* “Zinc Chloride as an Efficient Catalyst for Chemoselective Dimethyl Acetalisation, “ A. Ray, M. Rahman, S. Das, D. Kundu, S. K. Kundu, A. Majee and A. Hajra, Synth. Commun. 2009, 37, 590-595
24.* “Environmentally benign aqueous zinc tetrafluoroborate-catalyzed one-pot Biginelli condensation at room temperature” S. K. Kundu; A. Majee; A. Hajra Ind. J. Chem. 2009, 48B, 408-412
23. “Synthesis and charaterization of trans– [NiL2(NCS)2][ L = (2-aminomethyl) pyridine], trans– [NiL’2(NSC)2][ L’ = 2-(2-aminoethyl) pyridine] and trans– [NiL”2(NSC)2][ L” = 2-(2-methylaminoethyl) pyridine] complexes : X-ray single crystal structure of trans– [NiL’2(NSC)2][ L’ = 2-(2-aminoethyl) pyridine]” M. Ghosh, A. Majee, M. Nethaji, T. Chattopadhyay, Inorganica Chimica Acta 2009, 362, 2052-2055.
22.* “A facile synthesis of 2,2,4-trisubstituted-1,2-dihydroquinolines catalyzed by zinc triflate under solvent-free conditions” D. Kundu, S. K. Kundu, A. Majee, A. Hajra J. Chin. Chem. Soc. 2008, 55, 1186-1190
21.* “L-Proline Catalyzed Enamination of -Dicarbonyl Compounds under Solvent-free Conditions” D. Kundu, A. Majee, A. Hajra Chinese. J. Chem 2008, 26, 1545-1548.
20. “A novel single pot synthesis of binuclear copper(II) complexes of macrocyclic and macrocyclic compartmental ligands: Structures and magnetic properties” T. Chattapadhyay, K. S. Banu, A. Banerjee, J. Ribas, A. Majee, D. Das; J. Mol. Struc. 2007, 833, 13-22
19.* “A mild and efficient cleavage of oximes, hydrazones and semicarbazones using aqueous solution of zinc tetrafluoroborate”. A. Majee, S. K. Kundu J. Ind. Chem. Soc. 2007, 84,496-497
18. “Mono- and bimetallic Mn(II) complexes of macrocyclic salen type ligands: Synthesis, Characterisation and and studies of their catalytic activity”. T. Chattpadhayay; S. Islam; M. Nethaji; A. Majee; D. Das J. Molecular Cat. A, 2007, 267, 255-264
17.* “A Mild and Efficient Method for Oxathioacetalization of Carbonyl Compounds”. A. Majee, S. K. Kundu, S. Islam Synth. Commun. 2006, 36, 3767-3770
16. “Linkage isomerism in 1-(2-aminoethyl)morpholine (L) complexes of nickel(II)nitrite: X-ray single crystal structure of trans-[NiL2(NO2)2]” T. Chattopadhyay, M. Ghosh, A. Majee, M. Nethaji and D. Das Polyhedron 2005, 24, 1677-1681
15.* “Bromodimethylsulfonium bromide : A useful reagent for acetylation of alcohols, phenols, amines, thiols, thiophenols and 1,1-diacylation of aldehydes under solvent free condition” A.T. Khan, S. Islam, A. Majee, T. Chattopadhyay and S. Ghosh J. Molecular Cat. A, 2005, 239, 158-165
14.* “Tetrahydropyranylation and depyranylation of alcohols catalyzed by aqueous zinc tetrafluoroborate” S. Islam, A. Majee, A. T. Khan Synth. Commun. 2005, 35,1789-1793
13. “A highly efficient and catalytic synthetic protocol for oxathioacetalization of carbonyl compounds” A. T. Khan, P. R. Sahu, and A. Majee J. Molecular Cat. A, 2005, 226, 207-212
12*. “Selective Thioacetalization of Aldehydes Catalyzed by aqueous Zinc Tetrafluoroborate” S. Islam, A. Majee, T. Mandal and A. T. Khan, Synth. Commun. 2004, 34, 2911-2916
11. “The Mannich Reaction of Hydrazones amenable to Solid Phase Synthesis : A Powerful Tool for Heterocycle Preparation. V. Atlan, L. Elkaim, L. Grimaud, N. K. Jana and A. Majee, Synlett, 2002,352-354
10. “Hydrazones as Nucleophiles in Mannich Reaction” V. Atlan, L. Elkaim, H. Bienayme and A. Majee, J. Chem. Soc. Chem. Commun. 2000, 1585-1856
9. “An Ecofriendly Procedure for Selective Mono Acylation of Ferrocene on the Solid Phase of Alumina” B. C. Ranu, U. Jana and A. Majee, Green Chemistry, 1999, 33-34
8. “A Simple and Efficient Method for Selective Deprotection of Ter-butyldimethylsilyl Ethers by Zinc Tetrafluoroborate in Water” B. C. Ranu, U. Jana and A. Majee, Tetrahedron Lett. 1999, 40, 1985-1988
7. “Zinc Mediated Allylation of Aldehydes and Ketones Using Allyl Bromide and Commercial Zinc Dust. The Issue of Regio – and Stereoselectivity”, A. Majee , A. R. Das, B. C. Ranu, Ind. J. Chem. 1998, 37B,731-736
6. “One –pot Reductive Amination of Conjugated Aldehydes and Ketones with Silica gel and Zinc Borohydride” B. C. Ranu , A. Majee, A. Sarkar, J. Org. Chem. 1998,63, 370-373
5. “Reduction of Imines with Zinc Borohydride Supported on Silica Gel. Highly Stereoselective Synthesis of Substituted Cyclohexyl amines” B. C. Ranu, A. Sarkar, A. Majee J. Org. Chem. 1997,62,1841-1842.
4. “Indium Mediated Regioselective Markovnikov Allylation of Unactivated Terminal Alkynes” B. C. Ranu and A. Majee J. Chem. Soc. Chem. Commun. 1997, 1225-1226
3. “A Convenient Synthesis of ,-unsaturated Ketones Through Zinc Mediated Allylation of Acid Chlorides” B. C. Ranu , A. Majee and A. R. Das, Tetrahedron Lett. 1996, 37, 1109-1112
2. “Facile and Efficient Synthesis of Homoallyl Alcohols Using Allyl Bromide and Commercial Zinc Dust” B. C. Ranu , A. Majee, A. R. Das, Tetrahedron Lett. 1995, 36, 4885-4888
1. “Surface – Mediated Solid Phase Reaction Part 7. A Simple and Convenient
Procedure for Methoxymethylation of Alcohols with Methoxymethyl Chloride on the Surface of Alumina” B. C. Ranu, A. Majee, A. R. Das, Synth. Commun. 1995, 25,363-367