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1. Full Text Switching of Reaction Pathway from C−C Rollover to C−N Ring‐Extension Annulation
by Thenarukandiyil, Ranjeesh and Dutta, Champak and Choudhury, Joyanta
Chemistry – A European Journal, ISSN 0947-6539, 11/2017, Volume 23, Issue 61, pp. 15529 - 15533
This work discloses that a simple change in the anion of a copper(II) reagent along with the reaction solvent can dramatically alter the course of a Cp*Rh III... 
anion | chemoselectivity | annulation | C−H activation | rhodium | HETEROCYCLIC CARBENE | COUNTERION | ARENES | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | H BOND ACTIVATION | FUNCTIONALIZATION | CYCLOMETALATION | C-H activation | COUPLING REACTIONS | SELECTIVITY | RHODIUM CATALYSIS | Copper compounds | Carbon-carbon composites | Organic chemistry | Anions | Divergence | Rollover | Polarity | Chemical reactions | Basicity | Switching
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2. Full Text Palladium(0)-mediated C-H bond activation of N-(naphthyl)salicylaldimine and related ligands: utilization of the resulting organopalladium complexes in catalytic C-C and C-N coupling reactions
by Dutta, Jayita and Richmond, Michael G and Bhattacharya, Samaresh
Dalton Transactions, ISSN 1477-9226, 08/2015, Volume 44, Issue 30, pp. 13615 - 13632
N-(Naphthyl)-4-R-salicylaldimines (R = OCH3, H and Cl; H2L1-H2L3) and 2-hydroxy-N- (naphthyl)naphthaldimine (H2L4) readily undergo, upon reaction with... 
PALLADIUM(II) COMPLEXES | DESIGN | HETEROCYCLIC CARBENE | CARBON | CHEMISTRY | BENZALDEHYDE THIOSEMICARBAZONE COMPLEXES | ARYL | INDUCED PHOSPHORESCENT EMISSION | SUZUKI-MIYAURA | CHLORIDE | CHEMISTRY, INORGANIC & NUCLEAR
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3. Full Text Cross dehydrogenative coupling of: N -aryltetrahydroisoquinolines (sp3 C-H) with indoles (sp2 C-H) using a heterogeneous mesoporous manganese oxide catalyst
by Dutta, B and Sharma, V and Sassu, N and Dang, Y and Weerakkody, C and Macharia, J and Miao, R and Howell, A.R and Suib, S.L and Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Green Chemistry, ISSN 1463-9262, 2017, Volume 19, Issue 22, pp. 5350 - 5355
Here, we disclose a novel, heterogeneous catalytic approach for selective coupling of C1 of N-aryltetrahydroisoquinolines with C3 of indoles in the presence of... 
INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
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4. Palladium(0)-mediated C-H bond activation of N-(naphthyl)salicylaldimine and related ligands: utilization of the resulting organopalladium complexes in catalytic C-C and C-N coupling reactions
by Dutta, Jayita and Richmond, Michael G and Bhattacharya, Samaresh
Dalton Transactions, ISSN 1477-9226, 07/2015, Volume 44, Issue 30, pp. 13615 - 13632
N-(Naphthyl)-4-R-salicylaldimines (R = OCH sub(3), H and Cl; H sub(2)L super(1)-H sub(2)L super(3)) and 2-hydroxy-N-(naphthyl)naphthaldimine (H sub(2)L... 
Carbon-carbon composites | Catalysts | Mathematical analysis | Chemical reactions | Ligands | Activation | Palladium | Bonding
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5. Full Text Aryl Nitriles from Alkynes Using tert -Butyl Nitrite: Metal-Free Approach to C≡C Bond Cleavage
by Dutta, Uttam and Lupton, David W and Maiti, Debabrata
Organic Letters, ISSN 1523-7060, 02/2016, Volume 18, Issue 4, pp. 860 - 863
Alkyne C C bond breaking, outside of alkyne metathesis, remains an underdeveloped area in reaction discovery. Recently, nitrogenation has been reported to... 
AMBIENT CONDITIONS | ANTI-MARKOVNIKOV HYDRATION | CATALYZED CYCLOADDITION | 1,3-DIPOLAR CYCLOADDITION | SONOGASHIRA REACTION | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | CARBON TRIPLE BOND | RADICAL-ADDITION | STEREOSELECTIVE NITRATION | MOLECULAR-OXYGEN
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6. Summability theory C
: an introductory course in summability theory
by Aasma, Ants, 1957 and Dutta, Hemen, 1981 and Natarajan, P. N
2017, ISBN 9781119397694
Sequences (Mathematics) | Summability theory
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7. Land system in northern India, c. AD 400-c. AD 700
by Dutta, Saroj, 1952
1995, 1st ed., ISBN 9788121506571, xi, 224
Economic aspects | Agriculture | Finance, Public | History | Land use
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8. Full Text Measurement of the ratio of the production cross sections times branching fractions of B c ±  → J/ψπ ± and B± → J/ψK ± and ℬ B c ± → J / ψ π ± π ± π ∓ / ℬ B c ± → J / ψ π ± $$ \mathrm{\mathcal{B}}\left({\mathrm{B}}_{\mathrm{c}}^{\pm}\to \mathrm{J}/\psi {\pi}^{\pm }{\pi}^{\pm }{\pi}^{\mp}\right)/\mathrm{\mathcal{B}}\left({\mathrm{B}}_{\mathrm{c}}^{\pm}\to \mathrm{J}/\psi {\pi}^{\pm}\right) $$ in pp collisions at s = 7 $$ \sqrt{s}=7 $$ TeV
by Khachatryan, V and Sirunyan, A M and Tumasyan, A and Adam, W and Bergauer, T and Dragicevic, M and Erö, J and Fabjan, C and Friedl, M and Frühwirth, R and Ghete, V M and Hartl, C and Hörmann, N and Hrubec, J and Jeitler, M and Kiesenhofer, W and Knünz, V and Krammer, M and Krätschmer, I and Liko, D and Mikulec, I and Rabady, D and Rahbaran, B and Rohringer, H and Schöfbeck, R and Strauss, J and Taurok, A and Treberer-Treberspurg, W and Waltenberger, W and Wulz, C.-E and Mossolov, V and Shumeiko, N and Gonzalez, J Suarez and Alderweireldt, S and Bansal, M and Bansal, S and Cornelis, T and De Wolf, E A and Janssen, X and Knutsson, A and Luyckx, S and Ochesanu, S and Rougny, R and Van De Klundert, M and Van Haevermaet, H and Van Mechelen, P and Van Remortel, N and Van Spilbeeck, A and Blekman, F and Blyweert, S and D’Hondt, J and Daci, N and Heracleous, N and Keaveney, J and Lowette, S and Maes, M and Olbrechts, A and Python, Q and Strom, D and Tavernier, S and Van Doninck, W and Van Mulders, P and Van Onsem, G P and Villella, I and Caillol, C and Clerbaux, B and De Lentdecker, G and Dobur, D and Favart, L and Gay, A P. R and Grebenyuk, A and Léonard, A and Mohammadi, A and Perniè, L and Reis, T and Seva, T and Thomas, L and Vander Velde, C and Vanlaer, P and Wang, J and Zenoni, F and Adler, V and Beernaert, K and Benucci, L and Cimmino, A and Costantini, S and Crucy, S and Dildick, S and Fagot, A and Garcia, G and Mccartin, J and Ocampo Rios, A A and Ryckbosch, D and Salva Diblen, S and Sigamani, M and Strobbe, N and Thyssen, F and Tytgat, M and Yazgan, E and Zaganidis, N and ... and The CMS collaboration
Journal of High Energy Physics, ISSN 1029-8479, 1/2015, Volume 2015, Issue 1, pp. 1 - 30
The ratio of the production cross sections times branching fractions σ B c ± ℬ B c ± → J / ψ π ± / σ B ± ℬ B ± → J / ψ K ± $$ \left(\sigma... 
B physics | Branching fraction | Hadron-Hadron Scattering | Quantum Physics | Quantum Field Theories, String Theory | Classical and Quantum Gravitation, Relativity Theory | Physics | Elementary Particles, Quantum Field Theory
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9. Full Text Remote meta‐C–H Cyanation of Arenes Enabled by a Pyrimidine‐Based Auxiliary
by Bag, Sukdev and Jayarajan, Ramasamy and Dutta, Uttam and Chowdhury, Rajdip and Mondal, Rahul and Maiti, Debabrata
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2017, Volume 56, Issue 41, pp. 12538 - 12542
An easily removable pyrimidine‐based auxiliary has been employed for the remote meta ‐C−H cyanation of arenes. The scope of this Pd‐catalyzed cyanation... 
cyanation | palladium | C−H activation | pyrimidines | copper(I) cyanide | meta | meta-C−H activation | ROOM-TEMPERATURE | DIRECT ARYLATION | POTASSIUM HEXACYANOFERRATE(II) | CHEMISTRY, MULTIDISCIPLINARY | meta-C-H activation | DIRECT TRANSFORMATION | NITRILES | ARYL HALIDES | BOND ACTIVATION | TEMPLATE | PALLADIUM-CATALYZED CYANATION | BORYLATION | Pyrimidines | Palladium | Cyanides | Copper | Cyanide | Aromatic compounds
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10. Full Text Remote ‘Imidazole’ Based Ruthenium(II) p‐Cymene Precatalyst for Selective Oxidative Cleavage of C−C Multiple Bonds
by Dutta, Manali and Bania, Kusum Kumar and Pratihar, Sanjay
ChemCatChem, ISSN 1867-3880, 06/2019, Volume 11, Issue 11, pp. 2683 - 2694
The dual role of remote ‘imidazole’ attached with the precatalyst [( p ‐cymene)Ru II (L)Y] + (L=2‐(4‐substituted‐phenyl)‐1H‐imidazo[4,5‐f][1,10]... 
Oxidation | Ruthenium | Release of | Cymene | Dimethyl acetal | Imidazole
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11. Full Text An unusual werner type clathrate of Mn(II) benzoate involving energetically significant weak C–H⋯C contacts: A combined experimental and theoretical study
by Nashre-ul-Islam, Swah Mohd and Dutta, Debajit and Guha, Ankur K and Bhattacharyya, Manjit K
Journal of Molecular Structure, ISSN 0022-2860, 01/2019, Volume 1175, pp. 130 - 138
A new Werner type manganese(II) clatharate [Mn(Bz) (H O) ]∙(4–CNpy)∙2H O (1), where Bz = benzoate and 4–CNpy = 4–cyanopyridine, has been synthesized at room... 
Enclathration | C–H⋯C contact | Mn(II) clathrate | Supramolecular host | Crystal structure | Clathrate compounds | Structure | Analysis | Crystals
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12. Full Text Measurement of the branching fraction B (Λc+ →pK-π+)
by Zupanc, A and Bartel, C and Gabyshev, N and Adachi, I and Aihara, H and Asner, D.M and Aulchenko, V and Aushev, T and Bakich, A.M and Bala, A and Belous, K and Bhuyan, B and Bondar, A and Bonvicini, G and Bozek, A and Bračko, M and Browder, T.E and Červenkov, D and Chang, M.-C and Chekelian, V and Cheon, B.G and Chilikin, K and Chistov, R and Cho, I.-S and Cho, K and Chobanova, V and Choi, S.-K and Choi, Y and Cinabro, D and Dalseno, J and Danilov, M and DoleŽal, Z and Drásal, Z and Dutta, D and Dutta, K and Eidelman, S and Epifanov, D and Farhat, H and Fast, J.E and Feindt, M and Ferber, T and Gaur, V and Ganguly, S and Garmash, A and Gillard, R and Glattauer, R and Goh, Y.M and Golob, B and Haba, J and Hayasaka, K and Hayashii, H and He, X.H and Hoshi, Y and Hou, W.-S and Huschle, M and Hyun, H.J and Iijima, T and Ishikawa, A and Itoh, R and Iwasaki, Y and Iwashita, T and Jaegle, I and Julius, T and Kang, J.H and Kato, E and Kato, Y and Kawasaki, T and Kichimi, H and Kim, D.Y and Kim, H.J and Kim, J.B and Kim, J.H and Kim, M.J and Kim, Y.J and Kinoshita, K and Klucar, J and Ko, B.R and Kodyš, P and Korpar, S and KriŽan, P and Krokovny, P and Kronenbitter, B and Kuhr, T and Kumita, T and Kuzmin, A and Kwon, Y.-J and Lee, S.-H and Li, J and Li, Y and Libby, J and Liu, C and Liu, Y and Liu, Z.Q and Liventsev, D and Macnaughton, J and Miyabayashi, K and Miyata, H and Mizuk, R and Mohanty, G.B and Moll, A and ... and Belle Collaboration
Physical Review Letters, ISSN 0031-9007, 07/2014, Volume 113, Issue 4, p. 042002
We present the first model-independent measurement of the absolute branching fraction of the Λ(c)(+) → pK(-)π(+) decay using a data sample of 978 fb(-1)... 
Uncertainty | Statistical analysis | Asymmetry | Samples | Detectors | Decomposition | Recoilings | Baryons
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13. Full Text A measurement of the CP asymmetry difference between Λ c +  → pK − K + and pπ−π+ decays
by Aaij, R and Adeva, B and Adinolfi, M and Ajaltouni, Z and Akar, S and Albrecht, J and Alessio, F and Alexander, M and Alfonso Albero, A and Ali, S and Alkhazov, G and Alvarez Cartelle, P and Alves Jr, A A and Amato, S and Amerio, S and Amhis, Y and An, L and Anderlini, L and Andreassi, G and Andreotti, M and Andrews, J E and Appleby, R B and Archilli, F and d’Argent, P and Arnau Romeu, J and Artamonov, A and Artuso, M and Aslanides, E and Atzeni, M and Auriemma, G and Baalouch, M and Babuschkin, I and Bachmann, S and Back, J J and Badalov, A and Baesso, C and Baker, S and Balagura, V and Baldini, W and Baranov, A and Barlow, R J and Barschel, C and Barsuk, S and Barter, W and Baryshnikov, F and Batozskaya, V and Battista, V and Bay, A and Beaucourt, L and Beddow, J and Bedeschi, F and Bediaga, I and Beiter, A and Bel, L J and Beliy, N and Bellee, V and Belloli, N and Belous, K and Belyaev, I and Ben-Haim, E and Bencivenni, G and Benson, S and Beranek, S and Berezhnoy, A and Bernet, R and Berninghoff, D and Bertholet, E and Bertolin, A and Betancourt, C and Betti, F and Bettler, M O and van Beuzekom, M and Bezshyiko, Ia and Bifani, S and Billoir, P and Birnkraut, A and Bizzeti, A and Bjørn, M and Blake, T and Blanc, F and Blusk, S and Bocci, V and Boettcher, T and Bondar, A and Bondar, N and Bordyuzhin, I and Borghi, S and Borisyak, M and Borsato, M and Bossu, F and Boubdir, M and Bowcock, T J. V and Bowen, E and Bozzi, C and Braun, S and Brodzicka, J and Brundu, D and Buchanan, E and Burr, C and Bursche, A and ... and The LHCb collaboration and Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Journal of High Energy Physics, ISSN 1126-6708, 3/2018, Volume 2018, Issue 3, pp. 1 - 21
The difference between the CP asymmetries in the decays Λ c +  → pK − K + and Λ c +  → pπ − π + is presented. Proton-proton collision data taken at... 
Charm physics | CP violation | Hadron-Hadron scattering (experiments) | Flavor physics | Quantum Physics | Quantum Field Theories, String Theory | Classical and Quantum Gravitation, Relativity Theory | Physics | Elementary Particles, Quantum Field Theory | Skewed distributions | Luminosity | Statistical methods | Statistical analysis | Particle collisions | Decay | PHYSICS OF ELEMENTARY PARTICLES AND FIELDS
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14. Full Text Size controlled synthesis of Pd nanoparticles in water and their catalytic application in C–C coupling reactions
by Sawoo, Sudeshna and Srimani, Dipankar and Dutta, Piyali and Lahiri, Rima and Sarkar, Amitabha
Tetrahedron, ISSN 0040-4020, 2009, Volume 65, Issue 22, pp. 4367 - 4374
Catalytically active Pd nanoparticles have been synthesized in water by a novel reduction of Pd(II) with a Fischer carbene complex where polyethylene glycol... 
Water | C–C coupling | PEG | Pd nanoparticle | Fischer carbene complex | C-C coupling | ROOM-TEMPERATURE | ACETYLENE DERIVATIVES | CHEMISTRY, ORGANIC | HECK REACTIONS | SUZUKI-MIYAURA REACTION | AQUEOUS-SOLUTION | LIGAND-FREE PALLADIUM | ARYL HALIDES | RECYCLABLE CATALYST | COPPER-FREE | IONIC LIQUIDS | Nanoparticles | Palladium catalysts | Palladium | Polyethylene glycol
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15. Full Text Solventless C-C Coupling of Low Carbon Furanics to High Carbon Fuel Precursors Using an Improved Graphene Oxide Carbocatalyst
by Dutta, Saikat and Bohre, Ashish and Zheng, Weiqing and Jenness, Glen R and Núñez, Marcel and Saha, Basudeb and Vlachos, Dionisios G and Energy Frontier Research Centers (EFRC) (United States). Catalysis Center for Energy Innovation (CCEI)
ACS Catalysis, ISSN 2155-5435, 06/2017, Volume 7, Issue 6, pp. 3905 - 3915
Graphene oxide, decorated with surface oxygen ffinctionalities, has emerged as an alternative to precious-metal catalysts for many reactions. Herein, we report... 
C-C coupling | jet fuels | graphene oxide | biomass | fuel precursors | defects | OXIDATION | BIOMASS PLATFORM MOLECULES | ACID | SIN