345342-71-4Relevant articles and documents
Total synthesis of nafuredin, a selective NADH-fumarate reductase inhibitor.
Takano,Nagamitsu,Ui,Shiomi,Yamaguchi,Masuma,Kuwajima,Omura
, p. 2289 - 2291 (2001)
[structure: see text] Total synthesis of nafuredin, a selective NADH-fumarate reductase inhibitor, has been accomplished by a convergent approach. The C1-C8 and C9-C18 segments were derived efficiently from D-glucose and (S)-(-)-2-methyl-1-butanol, respectively, coupled by stereoselective Julia olefination, and converted to nafuredin.
Absolute configuration of nafuredin, a new specific NADH-fumarate reductase inhibitor
Takano, Daisuke,Nagamitsu, Tohru,Ui, Hideaki,Shiomi, Kazuro,Yamaguchi, Yuuichi,Masuma, Rokuro,Kuwajima, Isao,Mura, Satoshi
, p. 3017 - 3020 (2007/10/03)
Nafuredin, a new specific NADH-fumarate reductase inhibitor, was isolated from the culture broth of a fungal strain Aspergillus niger FT-0554. The stereoselective synthesis of three degradation products obtained by ozonolysis of nafuredin allowed elucidation of the absolute configuration of nafuredin.