Identification of an intermediate in autoxidation of carota-1,4-die-14-al into rugosal A
摘要:
In the autoxidation of (7R,10R)-carota-1,4-dien-14-al 1, which is a precursor of an antifungal compound rugosal A 2, in Rosa rugosa leaves, an intermediate possessing a 1,5-endoperoxy-2-hydroperoxy system 4 was isolated as a major product. The structures of compound 4 and other by-products including rugosal A 2 and rugosic acid A 3 were determined. These autoxidation products indicated the conversion pathway of compound 1 into rugosal A 2, similar to the radical reaction pathway in the autoxidation of polyunsaturated fatty acids.
Abstract A new sesquiterpene, (7 R ,10 R )-carota-1,4-dienaldehyde was identified in Rosarugosaleaves, and its structure elucidated by spectroscopic and chemical methods. The new compound was markedly unstable under air exposure to give several oxidized derivatives, in which rugosal A was found as the main product due to the 1,4-diene structure. The corresponding carboxylic acid, carota-1,4-dienoic
摘要 在蔷薇叶中鉴定出一种新的倍半萜(7 R ,10 R )-carota-1,4-二烯醛,并通过光谱和化学方法对其结构进行了阐明。新化合物在空气暴露下明显不稳定,产生了几种氧化衍生物,其中由于 1,4-二烯结构,发现 rugosal A 作为主要产物。在叶子中发现了相应的羧酸,carota-1,4-二烯酸。
Antimicrobial sesquiterpene from damaged Rosa rugosa leaves
Abstract An antimicrobialsesquiterpene has been isolated from diffusates of damagedleaves of Rosarugosa . Its structure, including relative stereochemistry, was deduced by chemical and spectroscopic (UV, IR, NMR and mass spectrometry) methods to be a novel carotane with an α,β-unsaturated aldehyde group, an endo -peroxide bridge and an allyl alcohol partial structure. The corresponding carboxylic
摘要 从蔷薇的受损叶片的扩散物中分离出一种抗菌倍半萜烯。其结构,包括相对立体化学,通过化学和光谱(紫外、红外、核磁共振和质谱)方法推断是一种具有α,β-不饱和醛基、内过氧化物桥和烯丙醇部分结构的新型胡萝卜素. 在 R. rugosa 的完整叶子中发现了相应的羧酸,但该化合物无真菌毒性。
HASHIDOKO, YASUYUKI;IWAYA, NORIKO;TAHARA, SATOSHI;, MIZUTANI JUNYA, AGR. AND BIOL. CHEM., 53,(1989) N, C. 2505-2507