@article{oai:nagasaki-u.repo.nii.ac.jp:00014221,
 author = {中尾, 英樹 and 新海, 征治 and 真鍋, 修},
 issue = {25},
 journal = {長崎大学工学部研究報告, Reports of the Faculty of Engineering, Nagasaki University},
 month = {Jul},
 note = {Flavins bearing an optically active substituent at N(10) (1-α and 1-b) were synthesized. As the substituent is sterically bulky, the rate constants for the oxidation of NADH model compounds which possibly proceeds via a face-to-face orientation were somewhat smaller than those of conventional flavins. We have found that the oxidation of optically active NADH model compounds by 1-b and tetra-O-acetylriboflavin occurs in an asymmetric manner. This is the first example for the in vitro asymmetric hydrogen transfer from NADH models to flavins., 長崎大学工学部研究報告, 15(25), pp.67-72; 1985},
 pages = {67--72},
 title = {光学活性基をもつフラビン類の合成とその不二水素移動反応},
 volume = {15},
 year = {1985}
}