A NOVEL CONSTRUCTION OF POLYFUNCTIONALIZED TRANS-HYDROINDANES VIA SULFUR-MEDIATED INTRAMOLECULAR DOUBLE MICHAEL TYPE REACTION

被引：15

作者：

IHARA, M

SUZUKI, S

TANIGUCHI, N

FUKUMOTO, K

KABUTO, C

机构：

[1] TOHOKU UNIV,INST PHARMACEUT,SENDAI,MIYAGI 980,JAPAN

[2] TOHOKU UNIV,FAC SCI,INSTRUMENTAL ANAL CTR CHEM,SENDAI,MIYAGI 980,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1991年 / 17期

关键词：

D O I：

10.1039/c39910001168

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

trans-Hydroindanes possessing an angular methyl group were stereoselectively synthesised via treatment of the four geometrical isomers 1a-1d of 9-methoxycarbonyl-4-methyl-1-phenylthionona-1,8-dien-3-one with tert-butyldimethylsilyl trifluoromethanesulphonate in the presence of triethylamine.

引用

页码：1168 / 1169

页数：2