Novel Aplysinopsin-Type Alkaloids from Scleractinian Corals of the Family Dendrophylliidae of the Mediterranean and the Philippines. Configurational-assignment criteria, stereospecific synthesis, and photoisomerization
作者:Graziano Guella、Ines Mancini、Helmut Zibrowius、Francesco Pietra
DOI:10.1002/hlca.19880710412
日期:1988.6.15
scleractinian coral Tubastraea sp. (Dendrophylliidae) collected at Palawan, Philippines, 3′-deimino-3′-oxoaplysinopsin (4) and 6-bromo-3′-deimino-3′-oxoaplysinopsin (6) are now isolated as 5:2 mixtures of (E/Z) stereoisomers. The 3′-deimino-2′,4′-bis(demethyl)-3′-oxoaplysinopsin (7) and 6-bromo-3′-demino-2′,4-bis(demethyl)-3′-oxoaplysinopsin (5) are isolated as 2:3 and 1:1 (E/Z) mixtures, respectively
来自巩膜珊瑚Tubastraea sp。(3)-deimino-3'-oxoaplysinopsin(4)和6-bromo-3'-deimino-3'-oxoaplysinopsin(6)收集于菲律宾巴拉望岛(Dendrophylliidae),现以(E / Z)立体异构体。3'-deimino-2',4'-双(去甲基)-3'-氧皂甙酶(7)和6-bromo-3'-demino-2',4-双(去甲基)-3'-氧皂甙酶(5)分别以2:3和1:1(E / Z)混合物的形式从另一种树突藻(Leptopsammia pruvoti)中分离出来,收集在法国地中海沿岸的马赛附近。通过合成可获得用于完整结构确定所需的大量这些化合物和相关化合物。因此,吲哚-3-羧甲醛(9)或其6-溴衍生物14与乙内酰脲(15),3-甲基乙内酰脲(11)或1,3-二甲基乙内酰脲(10)的缩合产生具有高立体特异性的普遍的天然