345342-66-7Relevant academic research and scientific papers
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.
Stereoselective Synthesis of Chiral γ-Hydroxy-β-methyl Methylcarbinols
Chakraborty, Tushar K.,Thippeswamy, Devasamudram,Jayaprakash, Sarva
, p. 741 - 745 (2007/10/03)
A simple synthesis of chiral γ-hydroxy-β-methyl methylcarbinols 1 starting from disubstituted olefins 3 is achieved in three steps : hydroboration, oxidation and hydride reduction. In the first step, excellent regioselectivity is achieved with bulky hydro
