of 66%. 3-Aminopropylphosphinic acid was prepared from allylamine in three steps with an overall yield of 56%. These improved protocols allowed to obtain these commercially unavailable phosphinic analogues of glutamic acid and GABA for testing on potential molecular targets.
由
乙烯基次
膦酸二丁酯三步一锅法合成2-
氨基-4-(羟基次膦基)
丁酸,总收率为66%。以
烯丙胺为原料,分三步制备3-
氨基
丙基次膦酸,总收率为56%。这些改进的方案允许获得这些商业上无法获得的谷
氨酸和
GABA 的
次膦酸类似物,用于测试潜在的分子靶标。