HEPTALENEBIS(TRICARBONYLIRON)

被引:22
作者
VOGEL, E
KERIMIS, D
ALLISON, NT
ZELLERHOFF, R
WASSEN, J
机构
[1] Institut für Organische Chemie, Universität Köln, Köln, D-5000
来源
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1979年 / 18卷 / 07期
关键词
D O I
10.1002/anie.197905451
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis of substituted heptalenes, e.g 3 and 4, can be accomplished via the bis(tricarbonyliron) derivative 2 formed from 1 and benzylideneacetone(tricarbonyliron). This entry into the chemistry of substituted heptalenes is facilitated by a new heptalene synthesis involving protection of the central double bond of isotetralin by epoxidation. (Figure Presented.) Copyright © 1979 by Verlag Chemie, GmbH, Germany
引用
收藏
页码:545 / 546
页数:2
相关论文
共 20 条
[1]  
BIRCH AJ, 1976, TRANSITION METAL ORG, V1, P1
[2]   NEW METHODS FOR OXIDATION OF ALDEHYDES TO CARBOXYLIC ACIDS AND ESTERS [J].
COREY, EJ ;
GILMAN, NW ;
GANEM, BE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (20) :5616-&
[3]   HEPTALENE [J].
DAUBEN, HJ ;
BERTELLI, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1961, 83 (22) :4659-&
[4]   CYCLOADDITIONS OF PENTALENE AND AZULENE - FACILE HEPTALENE SYNTHESIS [J].
HAFNER, K ;
DIEHL, H ;
SUSS, HU .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1976, 15 (02) :104-106
[5]  
Hafner K., 1976, ANGEW CHEM, V88, P121
[6]  
IPPEN J, 1975, THESIS U KOLN
[7]  
Lindner H. J., 1976, ANGEW CHEM, V88, P123
[8]   CRYSTAL AND MOLECULAR-STRUCTURE OF DIMETHYL 1,2-HEPTALENEDICARBOXYLATE [J].
LINDNER, HJ ;
KITSCHKE, B .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1976, 15 (02) :106-107
[9]   EXPEDITIOUS SYNTHESIS OF HEPTALENE FROM NAPHTHALENE VIA A BIS-(BICYCLO[1.1.0]BUTANE) INTERMEDIATE [J].
PAQUETTE, LA ;
BROWNE, AR ;
CHAMOT, E .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1979, 18 (07) :546-547
[10]  
PAQUETTE LA, 1979, ANGEW CHEM, V91, P581