Garcia M, Rodriguez J, Jimenez C
Departamento de Quimica Fundamental e Industrial, Facultade de Ciencias, Universidade da Coruna, 15071 A Coruna, Spain.
J Nat Prod. 1999 Feb;62(2):257-60. doi: 10.1021/np980331d.
Four new diterpenoids with the briarane skeleton, (-)-4-deacetyljunceellolide D (2), (+)-11alpha, 20alpha-epoxyjunceellolide D (3), (-)-11alpha, 20alpha-epoxy-4-deacetyljunceellolide D (4), and (-)-11alpha, 20alpha-epoxy-4-deacetoxyjunceellolide D (5), (+)-junceellolide A (6) [the antipodal derivative of the known (-)-junceellolide A], along with three known briaranes, (-)-junceellolide D (1), (-)-junceellin (7), and (-)-praelolide (8), were isolated from the Indonesian gorgonian Junceella fragilis. The structures of the new compounds were established on the basis of extensive NMR studies and by comparison with the spectral data from other briarane compounds. The absolute configurations for four of the compounds were determined by the modified Mosher method and by unambiguous chemical interconversions.
从印度尼西亚柳珊瑚柔枝柳珊瑚(Junceella fragilis)中分离出四种具有刺柏烷骨架的新二萜类化合物,即(-)-4-去乙酰柔枝柳珊瑚内酯D(2)、(+)-11α,20α-环氧柔枝柳珊瑚内酯D(3)、(-)-11α,20α-环氧-4-去乙酰柔枝柳珊瑚内酯D(4)和(-)-11α,20α-环氧-4-去乙酰氧基柔枝柳珊瑚内酯D(5)、(+)-柔枝柳珊瑚内酯A(6)[已知的(-)-柔枝柳珊瑚内酯A的对映体衍生物],以及三种已知的刺柏烷类化合物,(-)-柔枝柳珊瑚内酯D(1)、(-)-柔枝柳珊瑚素(7)和(-)-前内酯(8)。新化合物的结构通过广泛的核磁共振研究并与其他刺柏烷类化合物的光谱数据进行比较得以确定。其中四种化合物的绝对构型通过改良的莫舍尔方法和明确的化学转化确定。