Kitayama T, Yamamoto K, Utsumi R, Takatani M, Hill R K, Kawai Y, Sawada S, Okamoto T
Department of Agricultural Chemistry, Faculty of Agriculture, Kinki University, Nara, Japan.
Biosci Biotechnol Biochem. 2001 Oct;65(10):2193-9. doi: 10.1271/bbb.65.2193.
Further investigation of the chemistry of the eleven-membered cyclic sesquiterpene, zerumbone, the major component of the wild ginger, Zingiber zerumbet Smith, has revealed a new selective epoxidation process, a further example of a novel Favorskii-initiated double ring contraction, and a regiospecific fragmentation of zerumbone dibromide derivatives. Several zerumbone derivatives were found to be selective inhibitors of the growth of gram-positive bacteria.
对野生姜黄(Zingiber zerumbet Smith)的主要成分——十一元环倍半萜姜酮的化学性质进行的进一步研究,揭示了一种新的选择性环氧化过程、一个由Favorskii引发的新型双环收缩的进一步实例,以及姜酮二溴化物衍生物的区域特异性裂解。发现几种姜酮衍生物是革兰氏阳性菌生长的选择性抑制剂。