2006
DOI: 10.1021/ol061637b
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Tetrabromo Hydrogenated Cardanol:  Efficient and Renewable Brominating Agent

Abstract: 2,4,4,6-Tetrabromo-3-n-pentadecyl-2,5-cyclohexadienone (TBPCO) has been synthesized and used as a new efficient, convenient, and environmentally friendly brominating agent.

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Cited by 42 publications
(25 citation statements)
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“…1,7,11,12 and, more recently, in the preparation of nanomaterials via self-assembly of cardanol-based molecules (nanotubes, nanofibers, gels, liquid crystals and micelles). 1,[13][14][15] On the other side the underivatized, phenol hydrogenated, cardanol presents promising characteristics as a biocompatible brominating reagent 16 and, as far as the medical field is concerned, as antioxidant, antiobesity and antidiabetics agent. [17][18][19] Furthermore, presently, a great and increasing interest is devoted, both from academia and industry, to the research of "green" surfactants and to the design of surfactants bearing natural structural motives (amino acids, sugars and fatty acids).…”
Section: Introductionmentioning
confidence: 99%
“…1,7,11,12 and, more recently, in the preparation of nanomaterials via self-assembly of cardanol-based molecules (nanotubes, nanofibers, gels, liquid crystals and micelles). 1,[13][14][15] On the other side the underivatized, phenol hydrogenated, cardanol presents promising characteristics as a biocompatible brominating reagent 16 and, as far as the medical field is concerned, as antioxidant, antiobesity and antidiabetics agent. [17][18][19] Furthermore, presently, a great and increasing interest is devoted, both from academia and industry, to the research of "green" surfactants and to the design of surfactants bearing natural structural motives (amino acids, sugars and fatty acids).…”
Section: Introductionmentioning
confidence: 99%
“…28,63 O processo apresentou vantagens em relação aos métodos anteriores, [59][60][61] devido à menor relação adsorvente:LCC técnico, adequação do tempo do material na coluna e significativos rendimentos de cardanol.…”
Section: Figura 4 Principais Sítios Reacionais Da Molécula Do Cardanolunclassified
“…24,28,33,67,68 Sua principal aplicação é na produção de derivados poliméricos e resinas, 20 considerando seu potencial como possível substituto aos derivados do petróleo.…”
Section: Avanços Oportunidades E Sustentabilidadeunclassified
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