(-)-[(8,8-二氯樟脑基)-磺基]-恶肼啶合成路线 (共 2 条)
反应条件
1: 1) 1,8-diazabicyclo<5.4.0>undec-7-ene (DBU), 2) 1,3-dichloro-5,5-dimethylhydantoin (DCDMH) / 1) ethyl acetate, room temp., 30 min, 2) 20 - 25 deg C (ice-water bath), 90 min View Scheme
参考文献
Tetrahedron Letters, , vol. 33, # 2 p. 161 - 164
反应条件
Yield given. Multistep reaction;
参考文献
Tetrahedron Letters, , vol. 33, # 2 p. 161 - 164