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Refinado por: Base de dados/Biblioteca: Elsevier ScienceDirect Journals remover Base de dados/Biblioteca: Royal Society Of Chemistry Journals 2008- remover Materials Research Database remover nível superior: Recursos Online remover
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Intramolecular hydroalkoxylation catalyzed inside a self-assembled cavity of an enzyme-like host structure
Intramolecular hydroalkoxylation catalyzed inside a self-assembled cavity of an enzyme-like host structure
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Intramolecular hydroalkoxylation catalyzed inside a self-assembled cavity of an enzyme-like host structure

Catti, L ; Tiefenbacher, K

Chemical communications (Cambridge, England), 2015-01, Vol.51 (5), p.892-894 [Periódico revisado por pares]

England

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2
Electrochemically dehydrogenative C-H/P-H cross-coupling: effective synthesis of phosphonated quinoxalin-2(1)-ones and xanthenes
Electrochemically dehydrogenative C-H/P-H cross-coupling: effective synthesis of phosphonated quinoxalin-2(1)-ones and xanthenes
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Electrochemically dehydrogenative C-H/P-H cross-coupling: effective synthesis of phosphonated quinoxalin-2(1)-ones and xanthenes

Li, Ke-Jing ; Jiang, Yang-Ye ; Xu, Kun ; Zeng, Cheng-Chu ; Sun, Bao-Guo

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (16), p.4412-4421 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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3
Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited
Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited
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Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited

Bryan, Marian C. ; Dunn, Peter J. ; Entwistle, David ; Gallou, Fabrice ; Koenig, Stefan G. ; Hayler, John D. ; Hickey, Matthew R. ; Hughes, Shaun ; Kopach, Michael E. ; Moine, Gerard ; Richardson, Paul ; Roschangar, Frank ; Steven, Alan ; Weiberth, Franz J.

Green chemistry : an international journal and green chemistry resource : GC, 2018, Vol.20 (22), p.5082-5103 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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4
Carbon dots: synthesis, formation mechanism, fluorescence origin and sensing applications
Carbon dots: synthesis, formation mechanism, fluorescence origin and sensing applications
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Carbon dots: synthesis, formation mechanism, fluorescence origin and sensing applications

Liu, Meng Li ; Chen, Bin Bin ; Li, Chun Mei ; Huang, Cheng Zhi

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (3), p.449-471 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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5
Continuous manufacturing - the Green Chemistry promise?
Continuous manufacturing - the Green Chemistry promise?
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Continuous manufacturing - the Green Chemistry promise?

Rogers, Luke ; Jensen, Klavs F

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (13), p.3481-3498 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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6
Production of 2,5-furandicarboxylic acid (FDCA) from 5-hydroxymethylfurfural (HMF): recent progress focusing on the chemical-catalytic routes
Production of 2,5-furandicarboxylic acid (FDCA) from 5-hydroxymethylfurfural (HMF): recent progress focusing on the chemical-catalytic routes
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Production of 2,5-furandicarboxylic acid (FDCA) from 5-hydroxymethylfurfural (HMF): recent progress focusing on the chemical-catalytic routes

Sajid, Muhammad ; Zhao, Xuebing ; Liu, Dehua

Green chemistry : an international journal and green chemistry resource : GC, 2018, Vol.2 (24), p.5427-5453 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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7
Solubilisation of a 2,2-diphenyl-1-picrylhydrazyl radical in water by β-cyclodextrin to evaluate the radical-scavenging activity of antioxidants in aqueous media
Solubilisation of a 2,2-diphenyl-1-picrylhydrazyl radical in water by β-cyclodextrin to evaluate the radical-scavenging activity of antioxidants in aqueous media
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Solubilisation of a 2,2-diphenyl-1-picrylhydrazyl radical in water by β-cyclodextrin to evaluate the radical-scavenging activity of antioxidants in aqueous media

Nakanishi, Ikuo ; Ohkubo, Kei ; Imai, Kohei ; Kamibayashi, Masato ; Yoshihashi, Yasuo ; Matsumoto, Ken-ichiro ; Fukuhara, Kiyoshi ; Terada, Katsuhide ; Itoh, Shinobu ; Ozawa, Toshihiko ; Fukuzumi, Shunichi

Chemical communications (Cambridge, England), 2015-05, Vol.51 (39), p.8311-8314 [Periódico revisado por pares]

England

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8
Recent advances in the Suzuki-Miyaura cross-coupling reaction using efficient catalysts in eco-friendly media
Recent advances in the Suzuki-Miyaura cross-coupling reaction using efficient catalysts in eco-friendly media
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Recent advances in the Suzuki-Miyaura cross-coupling reaction using efficient catalysts in eco-friendly media

Hooshmand, Seyyed Emad ; Heidari, Bahareh ; Sedghi, Roya ; Varma, Rajender S

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (3), p.381-45 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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9
Visible-light initiated aerobic oxidations: a critical review
Visible-light initiated aerobic oxidations: a critical review
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Visible-light initiated aerobic oxidations: a critical review

Zhang, Xu ; Rakesh, K. P ; Ravindar, L ; Qin, Hua-Li

Green chemistry : an international journal and green chemistry resource : GC, 2018, Vol.2 (21), p.479-4833 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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10
Facile fractionation of lignocelluloses by biomass-derived deep eutectic solvent (DES) pretreatment for cellulose enzymatic hydrolysis and lignin valorization
Facile fractionation of lignocelluloses by biomass-derived deep eutectic solvent (DES) pretreatment for cellulose enzymatic hydrolysis and lignin valorization
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Facile fractionation of lignocelluloses by biomass-derived deep eutectic solvent (DES) pretreatment for cellulose enzymatic hydrolysis and lignin valorization

Shen, Xiao-Jun ; Wen, Jia-Long ; Mei, Qing-Qing ; Chen, Xue ; Sun, Dan ; Yuan, Tong-Qi ; Sun, Run-Cang

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (2), p.275-283 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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