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

页码：545 / 546

页数：2

共 20 条

[11] CRYSTAL-STRUCTURE AND CONFORMATION OF BIS-(TRICARBONYLIRON)HEPTALENE [J].

STEGEMANN, J ;

LINDNER, HJ .

JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1979, 166 (02) :223-231

[12]

STEGEMANN J, 1977, TETRAHEDRON LETT, P2515

[13] STABLE HEPTALENES-3,8-DIBROMOHEPTALENE [J].

VOGEL, E ;

IPPEN, J .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1974, 13 (11) :734-735

[14] DIMETHYL 3,8-HEPTALENEDICARBOXYLATE [J].

VOGEL, E ;

HOGREFE, F .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1974, 13 (11) :735-735

[15] OCTALENE [J].

VOGEL, E ;

RUNZHEIMER, HV ;

HOGREFE, F ;

BAASNER, B ;

LEX, J .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1977, 16 (12) :871-872

[16]

VOGEL E, 1974, ANGEW CHEM, V86, P778

[17]

Vogel E., 1974, ANGEW CHEM, V86, P777

[18]

Vogel E., 1974, ANGEW CHEM INT EDIT, V13, P732

[19]

VOGEL E, 1974, ANGEW CHEM, V86, P779

[20]

VOGEL HV, 1977, ANGEW CHEM, V89, P909

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