PREPARATIVE DERIVATIZATION OF ENDO-DICYCLOPENTADIENE VIA METALATION

被引:2
作者
KUMAGAI, T
AGA, M
OKADA, K
ODA, M
机构
[1] OSAKA UNIV, FAC SCI, DEPT CHEM, TOYONAKA, OSAKA 560, JAPAN
[2] EHIME UNIV, FAC EDUC, DEPT CHEM, MATSUYAMA, EHIME 790, JAPAN
关键词
D O I
10.1246/bcsj.64.1428
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
endo-Dicyclopentadiene has been selectively metallated with the base complex BuLi.t-BuOK in hexane at the olefinic positions in the norbornene moiety and a number of derivatives prepared by reaction of the metallated intermediate with electrophilic reagents. In particular, bromodicyclopentadiene thus obtained is a useful stock precursor for lithiodicyclopentadiene.
引用
收藏
页码:1428 / 1430
页数:3
相关论文
共 7 条
[1]   UBER DIE KONSTITUTION DER CYCLOPENTADIEN-CARBONSAURE AUS CYCLOPENTADIEN-KALIUM [J].
ALDER, K ;
FLOCK, FH ;
HAUSWEILER, A ;
REEBER, R .
CHEMISCHE BERICHTE-RECUEIL, 1954, 87 (11) :1752-1759
[2]   UBER DIE SYNTHESE DES 8.9-DIHYDRO-INDENS AUS DICYCLOPENTADIEN [J].
ALDER, K ;
FLOCK, FH .
CHEMISCHE BERICHTE-RECUEIL, 1954, 87 (12) :1916-1922
[4]  
SCHLOSSER M, 1973, ANGEW CHEM, V85, P544
[5]  
STAHLE M, 1985, CHIMIA, V39, P229
[6]  
VERKRUIJSSE HD, 1986, RECL TRAV CHIM PAY B, V105, P66
[7]   THE MECHANISM OF THE DIELS-ALDER REACTION [J].
WOODWARD, RB ;
KATZ, TJ .
TETRAHEDRON, 1959, 5 (01) :70-89