The synthesis of the first benzannelated -15,16-dihydropyrene: An example of the reduction of the diatropicity of a 14π-electron system by benzannelation-Reference-Cited by-同舟云学术

The synthesis of the first benzannelated -15,16-dihydropyrene: An example of the reduction of the diatropicity of a 14π-electron system by benzannelation

Published:1975-01 Issue:49 Volume:16 Page:4331-4334
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mitchell Reginald H.,Carruthers Robert J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference36 articles.

1. The Synthesis of Tetradehydrobenzocyclotetradecenes(?Benzodidehydro[14]annulenes?). The Effect of Benzoannelation on the Diamagnetic Ring Current of Macrocyclic (4n + 2) ?-Electron Systems

2. Synthesis and properties of benzo[c]-7,10,14-tri--butyl-1,8-didehydro[14]annulene

3. Dinaphtho[2,1-f:2′,1′-m]-3,10-DI--1,8-didehydro[14]annuleme. A diatropic annelated annulene

4. Synthesis and properties of diatropic naphtho[2,1-f]-dihydronaphtho[3′,4′,-m]-3,10-di-t-butyl-1,8- didehydro[14]annulene and a bis-dihydronaphtho analogue

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