Absolute Configuration of Actinophyllic Acid As Determined through Chiroptical Data

详细信息    查看全文

• 作者：Tohru Taniguchi ; Connor L. Martin ; Kenji Monde ; Koji Nakanishi ; Nina Berova ; Larry E. Overman
• 刊名：Journal of Natural Products
• 出版年：2009
• 出版时间：March 27, 2009
• 年：2009
• 卷：72
• 期：3
• 页码：430-432
• 全文大小：111K
• 年卷期：v.72,no.3(March 27, 2009)
• ISSN：1520-6025

文摘

The absolute configuration of actinophyllic acid (−)-1, an alkaloid with an unprecedented 2,3,6,7,9,13c-hexahydro-1H-1,7,8-(methanetriyloxymethano)pyrrolo[1′,2′:1,2]azacino[4,3-b]indole-8(5H)-carboxylic acid skeleton isolated from Alstonia actinophylla, was determined through the study of its corresponding methyl ester 2. Racemic 2 was separated into (+)-2 and (−)-2 enantiomers, and they were assigned unambiguously as 15S,16R,19R,20R,21S and 15R,16S,19S,20S,21R, respectively, by the use of optical rotation and electronic circular dichroism. Finally, (−)-2 was characterized as the methyl ester of naturally occurring (−)-1. The assigned 15R,16S,19S,20S,21R-configuration of (−)-1 is consistent with a proposed biosynthetic pathway.