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 CH 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 CH 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
|