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1-(2-Naphthyl)benzimidazolium based tripod for fluorescence enhancement based recognition of surfactants in water
1-(2-Naphthyl)benzimidazolium based tripod for fluorescence enhancement based recognition of surfactants in water
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1-(2-Naphthyl)benzimidazolium based tripod for fluorescence enhancement based recognition of surfactants in water

Kumar, Sandeep ; Arora, Shafali ; Singh, Prabhpreet ; Kumar, Subodh

RSC advances, 2012-01, Vol.2 (26), p.9969 [Periódico revisado por pares]

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2
1,1-Difluoroethyl chloride (CHCFCl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids
1,1-Difluoroethyl chloride (CHCFCl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids
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1,1-Difluoroethyl chloride (CHCFCl), a novel difluoroalkylating reagent for 1,1-difluoroethylation of arylboronic acids

Liu, Jianchang ; Zhang, Jida ; Wu, Chaolin ; Liu, Hefu ; Liu, Hui ; Sun, Fenggang ; Li, Yueyun ; Liu, Yuying ; Dong, Yunhui ; Li, Xinjin

RSC advances, 2019-09, Vol.9 (49), p.2849-28413 [Periódico revisado por pares]

England: Royal Society of Chemistry

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3
1,1-Dioxothiomorpholines with asymmetric environments: protecting group directed diastereoselectivity of glyco divinyl sulfone cyclization
1,1-Dioxothiomorpholines with asymmetric environments: protecting group directed diastereoselectivity of glyco divinyl sulfone cyclization
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1,1-Dioxothiomorpholines with asymmetric environments: protecting group directed diastereoselectivity of glyco divinyl sulfone cyclization

Bhaumik, Atanu ; Pal, Tarun Kumar ; Pathak, Tanmaya

RSC advances, 2015-01, Vol.5 (35), p.27706-27710 [Periódico revisado por pares]

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4
1,10-Phenanthroline-2,9-dicarboxamides as ligands for separation and sensing of hazardous metals
1,10-Phenanthroline-2,9-dicarboxamides as ligands for separation and sensing of hazardous metals
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1,10-Phenanthroline-2,9-dicarboxamides as ligands for separation and sensing of hazardous metals

Alyapyshev, M. ; Ashina, J. ; Dar’in, D. ; Kenf, E. ; Kirsanov, D. ; Tkachenko, L. ; Legin, A. ; Starova, G. ; Babain, V.

RSC advances, 2016-01, Vol.6 (73), p.68642-68652 [Periódico revisado por pares]

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5
1,10-Phenanthroline-based periodic mesoporous organosilica: from its synthesis to its application in the cobalt-catalyzed alkyne hydrosilylation
1,10-Phenanthroline-based periodic mesoporous organosilica: from its synthesis to its application in the cobalt-catalyzed alkyne hydrosilylation
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1,10-Phenanthroline-based periodic mesoporous organosilica: from its synthesis to its application in the cobalt-catalyzed alkyne hydrosilylation

Lin, Xiao-Tao ; Ishizaka, Yusuke ; Maegawa, Yoshifumi ; Takeuchi, Katsuhiko ; Inagaki, Shinji ; Matsumoto, Kazuhiro ; Choi, Jun-Chul

RSC advances, 2023-03, Vol.13 (12), p.7828-7833 [Periódico revisado por pares]

England: Royal Society of Chemistry

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6
1,1,3,3-Tetramethylguanidinium hydrogen sulphate (TMG·HSO 4 ) ionic liquid in carbon dioxide enriched water: a highly efficient acidic catalytic system for the hydrolysis of cellulose
1,1,3,3-Tetramethylguanidinium hydrogen sulphate (TMG·HSO 4 ) ionic liquid in carbon dioxide enriched water: a highly efficient acidic catalytic system for the hydrolysis of cellulose
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1,1,3,3-Tetramethylguanidinium hydrogen sulphate (TMG·HSO 4 ) ionic liquid in carbon dioxide enriched water: a highly efficient acidic catalytic system for the hydrolysis of cellulose

Kumar, Subodh ; Singh, Raj Kumar ; Jain, Suman L.

RSC advances, 2014-01, Vol.4 (102), p.58238-58242 [Periódico revisado por pares]

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7
1,1′-Dibenzyl-bis-(triazolyl)diphenylphosphine dioxide: a new efficient organocatalyst for silicon tetrachloride-mediated enantioselective Abramov-type phosphonylation of aldehydes with trialkyl phosphites
1,1′-Dibenzyl-bis-(triazolyl)diphenylphosphine dioxide: a new efficient organocatalyst for silicon tetrachloride-mediated enantioselective Abramov-type phosphonylation of aldehydes with trialkyl phosphites
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1,1′-Dibenzyl-bis-(triazolyl)diphenylphosphine dioxide: a new efficient organocatalyst for silicon tetrachloride-mediated enantioselective Abramov-type phosphonylation of aldehydes with trialkyl phosphites

Sevrain, Nicolas ; Volle, Jean-Noël ; Pirat, Jean-Luc ; Ayad, Tahar ; Virieux, David

RSC advances, 2017, Vol.7 (82), p.52101-52104 [Periódico revisado por pares]

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8
1,1′-Sulfinyldipyridinium bis (hydrogen sulfate) ionic liquid: synthesis and application in the temperature-influenced synthesis of novel pyranopyrimidinediones and pyranopyrimidinetriones
1,1′-Sulfinyldipyridinium bis (hydrogen sulfate) ionic liquid: synthesis and application in the temperature-influenced synthesis of novel pyranopyrimidinediones and pyranopyrimidinetriones
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1,1′-Sulfinyldipyridinium bis (hydrogen sulfate) ionic liquid: synthesis and application in the temperature-influenced synthesis of novel pyranopyrimidinediones and pyranopyrimidinetriones

Patil, Jayavant D. ; Korade, Suyog N. ; Pore, Dattaprasad M.

RSC advances, 2014-01, Vol.4 (92), p.50449-50455 [Periódico revisado por pares]

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9
1,2-Benzoxathiin-4(3 H )-one 2,2-dioxide - new enol nucleophile in three-component interaction with benzaldehydes and active methylene nitriles
1,2-Benzoxathiin-4(3 H )-one 2,2-dioxide - new enol nucleophile in three-component interaction with benzaldehydes and active methylene nitriles
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1,2-Benzoxathiin-4(3 H )-one 2,2-dioxide - new enol nucleophile in three-component interaction with benzaldehydes and active methylene nitriles

Grygoriv, Galyna V ; Lega, Dmitry A ; Chernykh, Valentin P ; Zaprutko, Lucjusz ; Gzella, Andrzej K ; Pawełczyk, Anna ; Shemchuk, Leonid A

RSC advances, 2018-01, Vol.8 (65), p.37295-37302 [Periódico revisado por pares]

England: Royal Society of Chemistry

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10
1,2-Difunctionalizations of alkynes entailing concomitant C-C and C-N bond-forming carboamination reactions
1,2-Difunctionalizations of alkynes entailing concomitant C-C and C-N bond-forming carboamination reactions
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1,2-Difunctionalizations of alkynes entailing concomitant C-C and C-N bond-forming carboamination reactions

Nanda, Santosh Kumar ; Mallik, Rosy

RSC advances, 2022-02, Vol.12 (1), p.5847-587 [Periódico revisado por pares]

England: Royal Society of Chemistry

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