作者:David Nichols、Juan Cueva
DOI:10.1055/s-0028-1083359
日期:——
efficient synthesis of the dopamine D1 selective full agonist dihydrexidine has been achieved in high yields and requiring no chromatographic separations via a facilitated intramolecular Henry cyclization of a (nitropropyl)benzophenone and subsequent diastereomerically selective reduction of the resulting tricyclic nitroalkene. acylations - intramolecular Henry reaction - nitroalkene - total synthesis.
高产率地实现了多巴胺D 1选择性全激动剂二氢己定的有效合成,并且不需要通过(硝基丙基)二苯甲酮的分子内亨利环化和随后的非对映异构选择性还原得到的三环硝基烯而进行色谱分离。 酰化-分子内Henry反应-硝基烯烃-全合成。