178762-28-2Relevant academic research and scientific papers
Convenient synthesis of 3-Hydroxyquinolines via dakin oxidation: A short synthesis of Jineol
Ghorai, Sujit K.,Dasgupta, Mayukh,Dutta, Piyali,Dumeunier, Raphael,Mal, Sanjib,Patre, Rupesh,Kuilya, Tapan Kumar,Pal, Sitaram,Manjunath, Bhanu N.
supporting information, (2020/08/06)
A convenient synthesis of 3-hydroxyquinolines has been described via unprecedented Dakin oxidation of quinoline-3-carboxaldehydes. Subsequently, application of the methodology to a high yielding synthesis of quinoline alkaloid Jineol (1) is reported.
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
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Page/Page column 11, (2008/06/13)
Compositions for the oxidative dyeing of keratin fibers, comprising a medium suitable for dyeing and at least one bicyclic 6-6 (0:1, 0:2, 1:1, 1:2) aza heteroaromatic keratin dyeing compound with one or two N-oxides. A method for oxidative dyeing of kerat
An efficient facile and selective hydroxylation of nitrogen heterocycles
Nasreen, Aayesha,Adapa, Srinivas R.
, p. 501 - 506 (2007/10/03)
Nitrogen heterocycles have been efficiently hydroxylated under mild and neutral conditions by employing Cupric nitrate/phosphate buffer/30%hydrogen peroxide system. The present method afforded the biologically active and important hydroxy heterocycles. Th
Preparation of new 3-hydroxyquinoline alkaloid, jineol and its ether derivatives using directed ortho-lithiation of chloroquinoline as the key step
Tagawa, Yoshinobu,Yamashita, Hiroyuki,Nomura, Manami,Goto, Yoshinobu
, p. 2379 - 2387 (2007/10/03)
A new alkaloid, jineol (3,8-dihydroxyquinoline) was conveniently prepared employing directed ortho-lithiation of chloroquinoline for 3-position of quinoline ring. Moreover, the ether derivatives of jineol were obtained by the reaction of jineol with alkyl
