N-[1-(S)-苄氧羰基-3-苯基丙基]-L-丙氨酸合成路线 （共 2 条）
反应条件
1: DCC / tetrahydrofuran / Ambient temperature 2: 1) tBuOK / 1) THF, -50 deg C, 20 min, 2) THF, -30 deg C, 20 min 3: ethyl acetate; diisopropyl ether / 3 h / Ambient temperature 4: H2 / Pd / methanol / 2 h / 760 Torr / Ambient temperature View Scheme
参考文献
Hayashi, Kimiaki; Nunami, Ken-ichi; Kato, Jyoji; Yoneda, Naoto; Kubo, Masami; et al.
Journal of Medicinal Chemistry, 1989 , vol. 32, # 2 p. 289 - 297
反应条件
1: DCC / tetrahydrofuran / Ambient temperature
2: 1) tBuOK / 1) THF, -50 deg C, 20 min, 2) THF, -30 deg C, 20 min
View Scheme
参考文献
Hayashi, Kimiaki; Nunami, Ken-ichi; Kato, Jyoji; Yoneda, Naoto; Kubo, Masami; et al.
Journal of Medicinal Chemistry, 1989 , vol. 32, # 2 p. 289 - 297
