NEW, CONVENIENT SYNTHESIS OF HIGHLY ACIDIC TETRAARYLPROPENES

被引：2

作者：

BAUER, H ^{[1
]}

MOERLER, C ^{[1
]}

REWICKI, D ^{[1
]}

机构：

[1] FREE UNIV BERLIN,INST ANORGAN CHEM,D-1000 BERLIN 33,FED REP GER

来源：

CHEMISCHE BERICHTE-RECUEIL | 1979年 / 112卷 / 04期

关键词：

D O I：

10.1002/cber.19791120442

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A New, Convenient Synthesis of Highly Acidic Tetraarylpropenes Fluorene, substituted fluorenes and azafluorenes, respectively, react with acetonitrile in the presence of powdered potassium hydroxide and molecular oxygen to give tetraarylpropenes in good yields. Copyright © 1979 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim

引用

页码：1473 / 1476

页数：4

共 9 条

[1]

FISCHER H, 1968, PROGR ORGANIC CHEM, P148

[2]

JUTZ C, 1964, CHEM BER, V97, P331

[3]

KUHLBRANDT W, UNPUBLISHED

[4]

KUHN R, 1965, LIEBIGS ANN CHEM, V690, P50

[5] ANIONEN UND FREIE RADIKALE ACIDER KOHLENWASSERSTOFFE UND IHRER AZA-ISOLOGEN [J].

KUHN, R .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1963, 75 (03) :174-&

[6]

KUHN R, 1962, LIEBIGS ANN CHEM, V654, P64

[7]

KUHN R, 1963, ANGEW CHEM INT EDIT, V2, P163

[8]

MOERLER C, 1978, THESIS FREIE U BERLI

[9]

ROTH K, 1973, THESIS FREIE U BERLI

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