Facile Redox Interconversion of 6,11-Diphenyldibenzo[b,f][1,4]diazocine and 2-(2-Aminophenyl)-1,3-diphenylisoindole: Reversible SET Ring Contraction and Expansion Processes-Reference-Cited by-同舟云学术

Facile Redox Interconversion of 6,11-Diphenyldibenzo[b,f][1,4]diazocine and 2-(2-Aminophenyl)-1,3-diphenylisoindole: Reversible SET Ring Contraction and Expansion Processes

Published:2014-10-14 Issue:33 Volume:2014 Page:7489-7498
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Eisch John J.,Liu Wei,Zhu Lisheng,Rheingold Arnold L.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference29 articles.

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2. Attempted Generation of the Potentially Aromatic 6,7-Diphenyldibenzo[e,g][1,4]diazocine Dianion Leads with Profound Rearrangement to the Isomeric N-(2-Amino-1,2-diphenylethenyl)carbazole Dianions

3. E N [2] 5b

4. 1 1 ortho 1 3 J. Org. Chem. 1963 28

5. Molecular Orbital Theory for Organic Chemists 1962

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3. Facile Rearrangement of the 6,11-Diphenyldibenzo[b,f][1,4]diazocine Skeleton into a Substituted 2-(2-Aminophenyl)-1,3-diphenylisoindole via Anomalous Carbolithiation or Hydrolithiation: Corroboration of Operative SET Processes;European Journal of Organic Chemistry;2015-10-16

4. Synthesis of Isoindoles by One-Electron Reductions of Dibenzo[1,4]diazocines;European Journal of Organic Chemistry;2014-12-16