Publications

Sl No. Manuscript Details Impact Factor citations
125 Fe(III) catalyzed peroxide mediated C-3 functionalizations of flavones: Bilal, A. M.; Banerjee, A.; Santra, S. K.; Rajamanickam, S.; Patel, B. K.* Adv. Synth. Catal. . 6.453 00
124 Synthesis of esters via sp3 C-H functionalisation: Majji, G.; Rout, S. K.;Rajamanikam, S.; Guin, S.; Patel, B. K.* Org. Biomol. Chem. (Review article, accepted) . 3.559 00
123 Peroxide free Pd(II)-catalyzed ortho-aroylation and ortho-halogenation of directing arenes: Santra, S. K.; Banerjee, A.; Mohanta, P. R.; Patel, B. K. * J. Org. Chem. (DOI: 10.1021/acs.joc.6b01170) . 4.785 00
122 Cs2CO3 as Source of carbonyl and ethereal oxygen in Cu-catalyzed cascade synthesis of benzofuran [3,2-c] quinolin[5-H]ones: Ali, W.; Modi, A.; Behere, A.; Prakash, R. M.; Patel, B. K. * Org. Biomol. Chem., 2016,14, 5940. . 3.559 00
121 Acyl-peroxy coumarins as ortho C-H acylating agent via a Pd(II) catalyzed redox neutral process: Mohanta, P. R.; Banerjee, A.; Santra, S. K.; Bahera, A.; Patel, B. K. * Adv. Synth. Catal., 2016, 358, 2047. . 6.453 00
120 N,N-Dimethylamide as a methylene synthon for regioselective linkage of imidazo[1,2-a]pyridine: Modi, A.; Ali, W.; Patel, B. K. * Adv. Synth. Catal., 2016, 358, 2100. . 6.453 00
119 PdII/CuBr2 catalysed keto α-Csp3-H benzoxylation of N,N-dialkylamides directed by o-hydroxy groups: Santra, S. K.; Banerjee, A.; Rajamanikam, S.; Khatun, N.; Patel, B. K. * Chem. Commun., 2016, 52, 4501. . 6.567 00
118 Copper(II)-catalyzed synthesis of -indoloquinoxalin-6-ones through oxidative Mannich reaction: Gogoi, A.; Sau, P.; Ali, W.; Guin, S.; Patel, B. K. * Eur. J. Org. Chem. 2016, 1499. . 3.065 00
117 Synthesis of 2-amino-substituted-1,3,4-thiadiazoles via 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) mediated intramolecular C-S bond formation in thiosemicarbazones: Singh, S. J.; Rajamanickam, S.; Gogoi, A.; Patel, B. K. * Tetrahedron Lett. 2016, 57, 1044. . 2.379 00
116 Copper-Catalysed Cascade Synthesis of Imidazolidine–Benzothiazole and Imidazolidine–Tetrazole Hybrid Heterocycles from Bis-thioureas by a Desulfurisation Strategy: Majji, G.; Sahoo, S. K.; Khatun, N.; Patel, B. K. * Eur. J. Org. Chem. 2015, 7534. . 3.065 00
115 Ruthenium(II) Catalyzed Regiospecific C–H/O–H Annulations of Directing Arenes via Weak Coordination: Banerjee, A.; Santra, S. K.; Mohanta, P. R.; Patel, B. K. * Org. Lett., 2015, 17, 5678. . 6.732 00
114 Bu4NI Catalyzed C-N Bond Formation via Cross-Dehydrogenative Coupling of Aryl Ethers (Csp3-H) and Tetrazoles (N-H): Rajamanickam, S.; Majji, G.; Santra, S. K.; Patel, B. K. * Org. Lett. 2015, 17, 5586. . 6.732 00
113 Palladium-Catalyzed Synthesis of 2-Aryl-2H-Benzotriazoles from Azoarenes and TMSN3: Khatun, N.; Modi, A.; Ali, W.; Patel, B. K. * J. Org. Chem. 2015, 80, 9662 . 4.785 00
112 Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C–N Bond Over C–S Bond Formation: Gogoi, A.; Guin, S.;Rajamanickam, S.; Rout, S. K.; Patel, B. K. * J. Org. Chem. 2015, 80, 18, 9016 . 4.785 00
111 CuO Nanoparticle Catalyzed Synthesis of 2,3-Disubstituted Quinazolinones via Sequential N-Arylation and Oxidative C–H Amidation: Modi, A.; Ali, W.; Mohanta, P. R.; Khatun, N.; Patel, B. K. * ACS Sustainable Chem. Eng., 2015, 3, 2582 . 4.642 00
110 Oxidant controlled regioselective mono- and di-functionalization reactions of coumarins: Banerjee, A.; Santra, S. K.; Khatun, N,; Ali, W.; Patel, B. K. * Chem. Commun., 2015, 51, 15422 . 6.567 00
109 Benzyl bromides as aroyl surrogates in substrate directed Pd catalysed o-aroylation: Behera, A.; Ali, W.; Guin, S.; Khatun, N.; Mohanta , P. R.; Patel, B. K. * RSC Adv. 2015, 5, 33334 . 3.708 00
108 Benzylic ethers as arylcarboxy surrogates in substrate directed ortho C–H functionalisation catalysed by copper: Khatun, N.; Banerjee, A.; Santra, S. K.; Ali, W.; Patel, B. K.* RSC Adv. 2015, 5, 36461 . 3.708 00
107 Generation of bis-Acyl Ketals from Esters and Benzyl Amines Under Oxidative Conditions: Majji, G.; Rajamanickam, S.; Khatun, N.; Santra, S. K.; Patel, B. K.* J. Org. Chem. 2015, 80, 3440 . 4.785 00
106 Regiospecific Benzoylation of Electron-Deficient N-Heterocycles with Methylbenzenes via a Minisci-Type Reaction: Ali, W.; Behera, A.; Guin, S.; Patel, B. K. * J. Org. Chem., 2015, 80, 5625 . 4.785 00
105 Palladium catalyzed ortho-halogenation of 2-arylbenzothiazole and 2,3-diarylquinoxaline: Santra, S. K.; Banerjee, A.; Khatun, N.; Samanta, A.; Patel, B. K.* RSC Adv. 2015, 5, 11960 . 3.708 00
104 Nano CuO Catalyzed Cross Dehydrogenative Coupling (CDC) of Aldehydes to Anhydrides: Khatun, N.; Santra, S. K.; Banerjee, A.; Patel, B. K.* Eur. J. Org. Chem. 2015, 1309 . 3.154 00
103 Copper(I) Promoted Cycloalkylation-Peroxidation of Unactivated Alkenes via sp3 C-H Functionalisation: Banerjee, A.; Santra, S. K.; Mishra, A.; Khatun, N.; Patel, B. K.* Org. Biomol. Chem. 2015, 13, 1307 . 3.487 00
102 Ceric Ammonium Nitrate (CAN) Promoted Pd(II)-Catalyzed Substrate Directed o-Benzoxylation and Decarboxylative o-Aroylation: Santra, S. K.†; Banerjee, A.†; Khatun, N.; Patel, B. K.* Eur. J. Org. Chem. 2015, 350 . 3.154 00
101 Copper catalyzed cross dehydrogenative coupling of N,N-disubstituted formamides and phenols: a direct access to carbamates. Ali, W.; Rou, S. K.; Guin, S.; Modi, A.; Banerjee, A.; Patel, B. K.* Adv. Synth and Catal. 2015, 357, 515 . 6.453 00
100 Pd(II)-catalysed o-aroylation of directing arenes using terminal aryl alkenes and alkynes: Khatun, N.; Banerjee, A.; Santra, S. K.; Behera, A.; Patel, B. K.* RSC Adv. 2014, 4, 54532. 3.708 00
99 A Cu-catalysed synthesis of substituted 3-methyleneisoindolin-1-one: Gogoi, A.; Guin, S.; Rout, S. K.; Majji, G.; Patel, B. K.* RSC Adv. 2014, 4, 59902 . 3.708 00
98 Benzylamine as an arylcarboxy surrogate: A copper catalysed o-benzoxylation of 2-phenylpyridines using benzyl amines: Behera, A.; Rout, S. K.; Guin, S.; Patel, B. K.* RSC Adv. 2014, 4, 55115 . 3.708 00
97 Cyclic ethers to esters and monoesters to bis-esters with unconventional coupling partners via sp3 C-H activation under metal free conditions. Majji, G.; Guin, S.; Rout, S. K.; Behera, A.; Patel, B. K.* Chem Commun. 2014, 50, 12193 . 6.781 00
96 A metal free domino synthesis of 3-aroylindoles via two sp3 C-H activation. Gogoi, A.; Modi, A.; Guin, S.; Rout, S. K.; Das, D.; Patel, B. K.* Chem Commun. 2014, 10445 . 6.781 00
95 Thioesterification of alkylbenzenes with thiols via copper-catalyzed cross dehydrogenative coupling without directing group. Ali, W.; Guin, S.; Rout, S. K.; Gogoi, A.; Patel, B. K.* Adv. Synth. Catal. 2014, 356, 3099 . 5.542 00
94 Formation of imidazolidinebenzothiazole-Cu(II) complexes via a copper mediated room temperature C-H activation of imidazolidinecarbo-thiamides. Sahoo, S. K.; Jena, H. S.; Majji, G.; Patel, B. K.*. Synthesis. 2014, 1886 . 2.500 00
93 A palladium II-catalysed synthesis of alpha-ketoamides via Chemoselective Aroyl Addition to cyanamides. Guin, S.; Rout, S. K.; Gogoi, A.; Ali, W.; Patel, B. K.* Adv. Synth. Catal. 2014, 356, 2559 . 5.542 00
92 Copper-catalyzed esterification of alkylbenzenes with cyclic ethers and cycloalkanes via C(sp3)-H activation following cross-dehydrogenative coupling. Rout, S. K.; Guin, S.; Ali, W.; Gogoi, A.; Patel, B. K.* Org. Lett. 2014, 16, 3086 . 6.324 01+1
91 Terminal aryl alkenes and alkynes as arylcarboxy surrogates towards o-benzoxylation of 2-phenylpyridine catalyzed by copper. Rout, S. K.; Guin, S.; Gogoi, A.; Majji, G.; Patel, B. K.* Org. Lett. 2014, 16, 1614 . 6.324 03+1
90 2,3-Diarylquinoxaline directed mono ortho-aroylation via cross dehydrogenative coupling using aromatic aldehydes or alkylbenzenes as aroyl surrogate. Santra, S. K.; Banerjee, A.; Patel, B. K.* Tetrahedron, 2014, 70, 2422 . 2.817 00
89 Divergent reactivities of o-halo anilides with CuO nanoparticle in water: A green synthesis of benzoxazoles and o-hydroxy anilides. Khatun, N.; Guin, G.; Rout, S. K. Patel, B. K.* RSC Adv. 2014, 4, 10770 . 3.708 00
88 Palladium-catalysed regioselective aroylation and acetoxylation of 3,5-diarylisoxazole via ortho C-H functionalisations. Banerjee, A.; Bera, A.; Santra, S. K.; Guin, S.; Patel, B. K.* RSC Adv. 2014, 4, 8558 . 3.708 01
87 CuO nano catalysed synthesis of 2H-indazoles under a ligand free condition. Khatun, N.; Gogoi, A.; Basu, P.; Das, P.; Patel, B. K.* RSC Adv. 2014, 4, 4080 . 3.708 01
86 Iodine–catalysed oxidative cyclisation of acylhydrazones to 2,5-substituted 1,3,4-oxadiazoles. Majji, G.; Rout, S. K.; Guin, S.; Gogoi, A.; Patel, B. K.* RSC Adv. 2014, 4, 5357 . 3.708 01
85 Bromination of organic substrates with special reference to green chemistry. Nath, J.; Sarmah, B. J.; Patel, B. K.* Advances in Chemical Research. 2013, 19, 85 . Book Chapter 00
84 A ligand free copper (II) catalyst is as effective as a ligand assisted pd(II) catalyst towards intramolecular C-S bond formation via CH functionalization. Banerjee, A.; Santra, S. K.; Rout, S. K.; Patel, B. K.* Tetrahedron, 2013, 69, 9096 . 2.817 02
83 Directing group assisted copper-catalyzed chemoselective o-acylation of phenols and enols using alkylbenzenes. Rout, S. K.; Guin, S.; Banerjee, A.; Khatun, N.; Gogoi, A.; Patel, B. K.* Org. Lett. 2013, 15, 4106 . 6.324 07 +1
82 A copper-catalyzed synthesis of 3-arylindole via sp3 C-H bond activation followed by C-C and C-O bond formation. Gogoi, A.; Guin, S.; Rout, S. K.; Patel, B. K.* Org. Lett. 2013, 15, 1802 . 6.324 12 +1
81 Easy access to benzylic esters directly from alkyl benzenes under metal-free conditions. Majji, G.; Guin, S.; Gogoi, A.; Rout, S. K.; Patel, B. K.* Chem. Commun. 2013, 49, 3031 . 6.781 14 +3
80 Regioselective ortho-hydroxylation of 2-arylbenzothiazole via substrate directed C-H activation. Banerjee, A.; Bera, A.; Guin, S.; Rout, S. K.; Patel, B. K.* Tetrahedron, 2013, 69, 2175 . 2.817 05
79 Palladium-catalyzed ortho-aroylation of 2-arylbenzothiazoles and 2-arylbenzoxazoles with aldehydes. Banerjee, A.; Santra, S. K.; Guin, S.; Rout, S. K.; Patel, B. K.* Eur. J. Org. Chem. 2013, 1367 . 3.154 09
78 Cu(II) catalyzed chemoselective oxidative transformation of thiourea to thioamidoguanidine/2-aminobenzothiazole. Sahoo, S. K.; Khatun, N.; Gogoi, Anupal; Deb, A.; Patel, B. K.* RSC Adv. 2013, 3, 438 . 3.708 02
77 A one-pot strategy for the synthesis of 2-aminobenzothiazole in water by copper catalysis. Khatun, N.; Jamir, L.; Ganesh, M.; Patel, B. K.* RSC Adv. 2012, 2, 11557 . 3.708 03
76 Four tandem C-H activations: A sequential C-C and C-O bond making via a Pd-catalyzed cross dehydrogenative coupling (CDC) approach. Guin, S.; Rout, S. K.; Banerjee, A.; Nandi, S.; Patel, B. K.* Org. Lett. 2012, 14, 5294 . 6.324 42
75 Desulfurization strategy in the construction of azoles possessing additional nitrogen, oxygen or sulfur using a copper(I) catalyst. Guin, S.; Rout, S. K.; Gogoi, A.; Nandi, S.; Ghara, K. K.; Patel, B. K.* Adv. Synth. Catal. 2012, 354, 2757 . 5.542 02
74 Stable Cu(I) complexes with thioamidoguanidine possessing halide-bridge structure. Sahoo, S. K.; Khatun, N.; Jena, H. S.; Patel, B. K.* Inorg. Chem. 2012, 51, 10800 . 4.794 05
73 An "on-water" exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles. Rout, S. K.; Guin, S.; Nath, J.; Patel, B. K.* Green Chem. 2012, 14, 2491 . 6.852 20
72 Copper catalyzed oxidative esterification of aldehydes with alkylbenzenes via cross dehydrogenative coupling. Rout, S. K.; Guin, S.; Ghara, K. K.; Banerjee, A.; Patel, B. K.* Org. Lett. 2012, 14, 3982 . 6.324 32
71 Tandem synthesis of [1,2,4]-triazoles mediated by iodine-a regioselective approach. Guin, S.; Rout, S. K.; Khatun, N.; Ghosh, T.; Patel, B. K.* Tetrahedron. 2012, 68, 5066 . 2.817 03
70 A one-pot conversion of di-substituted thiourea to O-organyl aryl thiocarbamate using FeCl3. Sahoo, S. K.; Chakraborty, S.; Patel, B. K.* Journal of Sulfur Chemistry 2012, 33, 143 . 1.101 01
69 A one pot synthesis of [1,3,4]-oxadiazoles mediated by molecular iodine. Guin, S.; Rout, S. K.; Ghosh, T.; Khatun, N.; Patel, B. K.* RSC Adv. 2012, 2, 3180 . 3.708 04
68 Environmentally benign one-pot synthesis of cyanamides from dithiocarbamates using I2 and H2O2. Jamir, L.; Sinha, U. B.; Nath, J.; Patel, B. K.* Synth. Commum. 2012, 42, 951 . 1.060 01
67 Regioselective intramolecular arylthiolations by ligand free Cu and Pd catalyzed reaction. Sahoo, S. K.; Banerjee, A.; Chakraborty, S.; Patel, B. K.* ACS Cat. 2012, 2, 544 . 7.572 08
66 It is “thiazolidine-2,4-dione” and not thiohydantoins as the reaction product of monosubstituted thioureas and chloroacetylchloride. Yella, R.; Singh, R.; Ganesh, M.; Patel, B. K.*J. Sulfur. Chem. 2011, 33, 1. 1.101 00
65 Cu (II) catalyzed imine CH functionalization leading to synthesis of 2,5-substituted-1,3,4-oxadiazoles. Guin, S.; Ghosh, S.; Rout, S. K.; Banerjee, A.; Patel, B. K.*Org. Lett. 2011, 13, 5976. 6.324 30
64 The oxidative cleavage of an anti-Hugerschoff product: a mild environmentally benign one pot synthesis of ureas from isothiocyanates. Jamir, L.; Khatun, N.; Patel, B. K.* RSC Adv. 2011, 1, 447. 3.708 01
63 Tandem regioselective synthesis of tetrazole and related heterocycles using iodine. Yella, R.; Khatun, N.; Rout, S. R.; Patel, B. K.* Org. Biomol. Chem. 2011, 9, 3235. 3.487 15
62 Improved procedure for the preparation of isothiocyanates via iodine-mediated desulfurization of dithiocarbamic acid salts. Jamir. L.; Nath. J.; Patel, B. K.* Green Chem. Lett and Rev. 2011, 4, 1. 1.216 05
61 Bromineless bromine as an efficient desulfurizing agent for the preparation of cyanamides and 2-aminothiazoles from dithiocarbamate salts. Yella, R.; Kavala, V.; Patel, B. K.* Synth. Commum. 2011, 41, 792. 1.060 03
60 A convenient one-pot synthesis of aryl amines from aryl aldoximes mediated by Koser's reagent. Ghosh, H.; Banerjee, A.; Rout, S. K.; Patel, B. K.* Arkivoc, 2011, 2, 209. 1.076 01
59 Copper (I)-catalyzed cascade synthesis of 2-arylsulfanyl-arylcyanamides. Sahoo, S. K.; Jamir, L.; Guin, S.; Patel, B. K.* Adv. Synth and Catal. 2010, 352 (14-15), 2538. 5.542 17
58 One-pot synthesis of five and six membered N, O, S-heterocycles using a ditribromide reagent. Yella, R.; Patel, B. K.* J. Combi. Chem. 2010, 12, 754. 3.401 16
57 Arylthioureas with bromine or its equivalents gives No ‘Hugerschoff’ reaction product. Yella, R.; Murru, S.; Rezzak, A. R.; Patel, B. K.* Org. Biomol. Chem. 2010, 8, 3389. 3.487 11
56 Efficient preparation of isothiocyanates from dithiocarbamates using bromineless brominating reagent. Yella, R.; Ghosh, H.; Murru, S.; Sahoo, S. K.; Patel, B. K.* Synth. Commum. 2010, 40, 2083. 1.060 07
55 Oxidative desulfurization of disubstituted thioureas using Pb(II) salts and investigation of pKa-dependent regioselective N-acylation. Ghosh, H.; Sarkar, S.; Ali. A. R.; Patel, B. K.* J. Sulfur. Chem. 2009, 31, 1. 1.101 02
54 The thiocarbonyl ‘S” is softer than thiolate ‘S’: A catalyst-free one-pot synthesis of isothiocyanates in water. Jamir, L.; Ali, A. R.; Ghosh. H.; Francis, A. S. C.; Patel, B. K.* Org. Biomol. Chem. 2010, 8, 1674. 3.487 11
53 A greener synthetic protocol for the preparation of carbodiimide. Ali, A. R.; Ghosh, H.; Patel, B. K.* Tetrahedron Lett. 2010, 51, 1019. 2.391 13
52 Hypervalent iodine (III)-mediated oxidation of aldoximes to N-acetoxy or N-hydroxy amides. Ghosh. H.; Patel, B. K.* Org. Biomol. Chem. 2010, 8, 384. 3.487 15
51 Copper (I)-catalyzed cascade synthesis of 2-substituted benzothiazoles: A direct access to benzothiazolones. Murru, S.;. Mondal , P.; Yella, R.; Patel, B. K.* Eur. J. Org. Chem. 2009, 5406. 3.154 22
50 A one-pot preparation of cyanamide from dithiocarbamate using molecular iodine. Nath, J.; Patel, B. K.* Jamir, L.; Sinha, U. B.; Satyanarayana. K.V.V.V. Green Chem. 2009, 11, 1503. 6.852 23
49 A comprehensive decomposition analysis of stabilization energy (CDASE) and its application in locating the rate-determmining step and multi-step reactions. Bagaria, P.; Saha, S.; Murru, S.; Kavala, V.; Patel, B. K.* Ray, R. K. Phys. Chem. Chem. Phys., 2009, 11, 8306. 4.198 14
48 Intra- and intermolecular C-S bond formation using single catalytic system: first direct access to arylthiobenzothiazoles. Murru, S.; Ghosh, H.; Sahoo, S. K.; Patel, B. K.* Org. Lett. 2009, 11, 4254. 6.324 48
47 Acyl-isothiocyanates as efficient thiocyanate transfer reagents. Palsuledesai, C. C. Murru, S.; Sahoo, S. K.; Patel, B. K.* Org. Lett. 2009, 11, 3382. 6.324 12
46 Molecular iodine mediated preparation of isothiocyanate from dithiocarbamic acid salts. Nath, J.; Yella, R.; Ghosh, H.; Patel, B. K.* Eur. J. Org. Chem. 2009, 1849. 3.154 23
45 An efficient synthesis of cyanamide from amine promoted by a hypervalent iodine (III) reagent. Ghosh, H.; Yella, R.; Ali, A. R.; Sahoo, S. K.; Patel, B. K.* Tetrahedron Lett. 2009, 50, 2407. 2.391 25
44 Efficient one pot preparation of bis-alkylxanthogen disulfides from alcohols. Jamir. L.; Yella. R.; Patel, B. K.* J. Sulfur. Chem. 2009, 30, 128. 1.101 03
43 Copper (I)-catalyzed synthesis of substituted 2-mercapto benzamidazole. Murru, S.; Patel, B. K.* Bras, J. Le.; Muzart. J. J. Org. Chem. 2009, 74, 2217. 4.638 55
42 Desulfurization mediated by hypervalent iodine (III): A novel strategy for the construction of heterocycles. Ghosh, H.; Yella, R.; Nath, J.; Patel, B. K.* Eur. J. Org. Chem. 2008, 6189. 3.154 29
41 It is “2-imino-4-thiazolidinones” and not thiohydantoins as the reaction product of 1,3-disubstituted thioureas and chloroacetylchloride. Yella, R.; Ghosh, H.; Patel, B. K.* Green. Chem. 2008, 10, 1307. 6.852 24
40 A new facile synthetic method for the construction of 1,3-oxathiolane-2-ylidenes. Ghosh, H.; Singh, C. B.; Murru, S, Kavala, V.; Patel, B. K.* Tetrahedron Lett. 2008, 49, 2601. 2.391 05
39 Synthesis and regiochemistry of enolate addition to 9-phenyl-9H-xanthane-9-ol. Kavala, V.; Murru, S.; Das, G.; Patel, B. K.* Tetrahedron. 2008, 64, 3960. 2.817 06
38 Hypervalent Iodine (III) mediated regioselective N-acylation of 1,3-disubstituted thioureas. Singh, C. B.; Ghosh, H.; Murru, S.; Patel, B. K.* J. Org. Chem. 2008, 73, 2924. 4.638 33
37 A convenient one-pot synthesis of thiazole-2-imines: application to the construction of pifithrin analogues. Murru, S.; Singh, C. B.; Kavala, V.; Patel, B. K.* Tetrahedron. 2008, 64, 1931. 2.817 42
36 Aqueous-mediated N-alkylation of amines. [Erratum to document cited in CA146:521492]. Singh, C. B.; Kavala, V.; Samal, A. K.; Patel, B. K.* Eur. J. Org. Chem. 2007, 5441. 3.154 00
35 3-Aryl-1-benzoylthioureas with -bromoketones in water form 2-N-benzoyl-3-arylthiozole-2-(3H)-imine, not 3-aryl-1-benzoylimidazoline-2-thione. Singh, C. B.; Murru, S.; Kavala, V.; Patel, B. K.* J. Chem. Res. 2007, 136. 0.633 08
34 Self-assembled superstructure of xanthene derivatives. Kavala, V.; Murru, S.; Patel, B. K.* Das, G. J. Chem. Crystallogr. 2007, 527. 0.566 06
33 Aqueous-mediated N-alkylation of amines. Singh, C. B.; Kavala, V.; Samal, A. K.; Patel, B. K.* Eur. J. Org. Chem. 2007, 1369. 3.154 29
32 A one-pot synthesis of 1,4-dithiins and 1,4-benzodithiins from ketones using the recyclable reagent 1,1'-(ethane-1,2-diyl)dipyridinium bistribromide (EDPBT). Murru, Siva; Kavala, Veerababurao; Singh, C. B.; Patel, B. K.* Tetrahedron Lett. 2007, 48, 1007. 2.391 12
31 It Is "thiazolidene-2-imine" and not imidazole-2-thione as the reaction product of 1-benzoyl-3-phenylthiourea with Br2 / enolizable ketone. Singh, C. B.; Murru, S.; Kavala, V.; Patel, B. K.* Org. Lett. 2006, 8, 5397. 6.324 46
30 1,1’-(Ethane-1,2-diyl)dipyridinium-bistribromide (EDPBT) as a recyclable catalyst for acylation. Naik, S; Kavala, V; Gopinath, R; Patel, B. K.* ARKIVOC, 2006 (xi), 21. 1.076 08
29 Acetalization and thioacetalization of of cabonyl compounds: A case study based on global and local electrophilicity descriptors. Roy, R. K.;* Usha, V.; Patel, B. K.* Hirao, K. J. Comp. Chem. 2006, 27, 773. 3.601 19
28 Chemoselectivity in acetalization, thioacetalization, oxathioacetalization and azathioacetalization. Roy, R. K*.; Kavala, V.; Naik, S.; Patel, B. K.* J. Phys. Chem. 2006, 110, 2181. 2.775 23
27 Tetrabutylammonium tribromide mediated condensation of carboxylic acids with acohols. Naik, S.; Kavala, V.; Gopinath, R.; Patel, B. K.* ARKIVOC, 2006, (1), 119. 1.076 16
26 A new recyclable ditribromide reagent for efficient bromination under solvent free condition. Kavala, V.; Naik, S.; Patel, B. K.* J. Org. Chem. 2005, 70, 6556. 4.638 13
25 A new recyclable ditribromide reagent for efficient bromination under solvent free condition. Kavala, V.; Naik, S.; Patel, B. K.* J. Org. Chem. 2005, 70, 4267. 4.638 112
24 Reinvestigation of mechanism of gem-diacylation: chemoselective conversion of aldehydes to various gem-diacylates and their cleavage under acidic and basic conditions. Kavala, V.; Patel, B. K.* Eur. J. Org. Chem. 2005, 441. 3.154 28
23 Water as catalyst and solvent: tetrahydropyranylation of alcohols in an aqueous medium. Kavala, V.; Samal, A. K.; Patel, B. K.* Arkivoc 2005 (i), 29. 1.076 16
22 Mild and eco-friendly chemoselective acylation of primary amines in an aqueous medium. Naik, S.; Bhattacharjya G.; Kavala, V.; Patel, B. K.* Arkivoc 2004 (i), 55. 1.076 16
21 Chemoselective thioacetalization and transthioacetalization of carbonyl compounds catalysed by tetrabutylammonium tribromide (TBATB). Naik, S.; Gopinath, R.; Goswami, M.; Patel, B. K.* Org. Biomol. Chem. 2004, 2, 1670. 3.487 27
20 Chemoselective acylation of amines in aqueous media. Naik, S.; Bhattacharjya G.; Talukdar, B.; Patel, B. K.* Eur. J. Org. Chem. 2004, 1254. 3.154 51
19 Peroxovanadium catalysed oxidative esterification of aldehydes. Gopinath, R.; Barkakaty, B.; Talukdar, B.; Patel, B. K.* J. Org. Chem. 2003, 68, 2944. 4.638 59
18 V2O5-H2O2: A convenient reagent for the direct oxidation of acetals to esters. Gopinath, R.; Paital, A. R.; Patel, B. K.* Tetrahedron Lett. 2002, 43, 5123. 2.391 33
17 Tetrabutylammonium tribromide (TBATB) as an efficient generator of HBr for an efficient chemoselective reagent for acetalisation of carbonyl compounds. Gopinath, R.; Haque, Sk. J.; Patel, B. K.* J. Org. Chem. 2002, 67, 5842. 4.638 104
16 Tetrabutylammonium tribromide (TBATB) promoted tetrahydropyranylation / depyranylation of alcohols. Naik, S.; Gopinath, R.; Patel, B. K.* Tetrahedron Lett. 2001, 42, 7679. 2.391 94
15 Tetrabutylammonium tribromide (TBATB)-MeOH: An efficient chemoselective reagent for the cleavage of tert-butyldimethylsilyl (TBDMS) ethers. Gopinath, R.; Patel, B. K.* Org. Lett. 2000, 2, 4177. 6.324 68
14 A catalytic oxidative esterification of aldehydes using V2O5-H2O2.. Gopinath, R.; Patel, B. K.* Org. Lett. 2000, 2, 577. 6.324 109
13 Regioselective bromination of organic substrates by tetrabutylammonium bromide promoted by V2O5-H2O2: An environmentally favourable synthetic protocol. Bora, U.; Bose, G.; Chaudhuri, M. K.; Dhar, S. S.; Gopinath, R.; Khan, A. T.; Patel, B. K.* Org. Lett. 2000, 2, 247. 6.324 143
12 Incorporation of terminal phosphorothioates into oligonucleotides. Alefelder, S.; Patel, B. K. Eckstein, F. Nucleic Acids Res. 1998, 26, 4983. 8.808 51
11 An environmentally benign synthesis of organic ammonium tribromides (OATB) and bromination of selected organic substrates by tetrabutylammonium tribromide (TBATB). Chaudhuri, M. K.; Khan, A. T.; Patel, B. K.;* Dey, D.; Kharmawophlang, W.; Lakshmiprabha, T. R.; Mandal, G. C. Tetrahedron Lett. 1998, 39, 8163. 2.391 121
10 Properties of some diuridine phosphate analogues. Patel, B. K. Thomson, J. B.; Jimenez, V.; Eckart, K.; Eckstein, F.* Nucleosides and Nucleotides. 1997, 16, 1443. 0.894 01
9 5’-Deoxy-5’-thioribonucleoside-5’-triphosphates. Patel, B. K. Eckstein., F.* Tetrahedron Lett. 1997, 38, 1021. 2.391 08
8 Synthesis and properties of diuridinephosphate analogues containing thio- and amino- modifications. Thomson, J. B.; Patel, B. K. Jimenez, V.; Eckart, K.; Eckstein, F.* J. Org. Chem. 1996, 61, 6273. 4.638 81
7 Chemical synthesis of uridyl (3’-5’) thymidine phosphate analogues as models for ribozymes substrates. Thomson, J. B.; Patel, B. K.; Eckstein, F* J. Cellur. Bio Chem. 1995, 217. 3.368 02
6 Synthetic nucleases crafted from L-lysine. Ranganathan, D.;* Mishra, R.; Patel, B. K. Vaish. N. K. Proc. Indian Acad. Sci. (Chem. Sci.) 1994, 106, 1071. 0.891 06
5 Design of a simple and flexible dimeric peptide model for DNA recognition and scission. Ranganathan, D.;* Patel, B. K. Mishra., R. J. Chem. Soc., Chem. Commu. 1994, 107. 6.781 08
4 Design of chemical nuclease model with (Lys)2Cu as the core motif. Ranganathan, D.;* Patel, B. K. Mishra. R. K. J. Chem. Soc., Chem. Commun. 1993, 337. 6.781 01
3 Lysine-sandwiched ionophores. Ranganathan, S.; Patel, B. K. Tetrahedron Lett. 1993, 34, 2533. 2.391 04
2 Demonstration of exclusive peptidation at the micellar interface. Ranganathan, D.; Ranganathan, S.; Singh, G. P.; Patel, B. K. Tetrahedron Lett. 1993, 34, 525. 2.391 07
1 Chemical approaches to the re-structuring of proteins. Ranganathan, S.;* Ranganathan, D.; Bemezai, S.; Singh, W. P.; Bhattacharyya, D.; Singh, G. P.; Rathi, R.; Saini, S.; Jayaraman, N.; Patel, B. K. Pure and Appl. Chem. 1990, 62, 1437. 3.112 05