444-15-5Relevant articles and documents
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Endo,Okawara
, p. 1487,1488 (1977)
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Bieri,May
, p. 981 (1977)
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Selective Reduction by 2-Amino-4-methylpyridine Borane and 2-Aminopyrimidine Borane
Okamoto, Yoshihisa,Osawa, Toshimitsu,Kurasawa, Yoshihisa,Kinoshita, Toshio,Takagi, Kaname
, p. 1383 - 1385 (2007/10/02)
Stereo- and chemoselective reductions and synthetic utility of the title compounds are described.
Reduction of Vicinal Tricarbonyl Compounds by Reduced Nicotinamide Adenine Dinucleotide Model and Electron-Transport Systems
Endo, Takeshi,Okawara, Makoto
, p. 2663 - 2666 (2007/10/02)
The reduction of vicinal tricarbonyl compounds such as alloxan (A) and ninhydrin (NY) with 1-benzyl-1,4-dihydronicotinamide (BNAH; NADH model) was investigated.In the reduction of A with BNAH, the radical anion (A-.Py+) of A as the 1-benzyl-3-carbamoylpyridinium salt and the dialuric acid (D) was obtained by one-electron and two-electron reduction,respectively.Similarly,hydrindantin (HDT) and 2-hydroxy-1,3-indandione (HID) were also afforded in the reduction of NY with BNAH.Further,the reductions of alloxantin (AT) and HDT with BNAH were performed to give D and HID,respectively.The reduction of lipoic acid (LA) and viologens (V2+) with BNAH, which could not be reduced without A or NY, proceeded smoothly in their presence,and they proved to be useful as mediators for catalytic reduction of LA and V2+.