276. Cyclisations with hydrazine. Part I. The preparation of phenanthrene compounds and of pyrene from aldehydes. A variation in reductions of the Wolff

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276. Cyclisations with hydrazine. Part I. The preparation of phenanthrene compounds and of pyrene from aldehydes. A variation in reductions of the Wolff–Kishner type

Published:1958 Issue:0 Volume:0 Page:1375-1381
ISSN:0368-1769
Container-title:J. Chem. Soc.
language:en
Short-container-title:J. Chem. Soc.

Author:

Bacon R. G. R.,Lindsay W. S.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1958/JR/JR9580001375

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1. Synthesis of an Anion Receptor Using 3,6-Diaminophenanthrene as a Scaffold;Molbank;2024-07-19

2. Rediscovering Bacon's hydrazine/phenylhydrazine mediated cyclization of 2,2′-dicarbonylbi(hetero)aryls: construction of (5-azo)-/indazolo[2,3-a]quinolines;Organic & Biomolecular Chemistry;2022

3. The conformational space of diphenylamine-2,2'-dicarboxaldehyde. “Whoever reports a saying in the name of the one who said it brings redemption to the world.”;Structural Chemistry;2019-02-21

4. Progress of pyrene-based organic semiconductor in organic field effect transistors;Science China Chemistry;2016-11-15

5. Comparison of Ullmann/RCM and Ullmann/Bis-hydrazone Coupling Reactions; New Access to Benzodithiophenes for Dye-Sensitized Solar Cell and Thiahelicene Applications;Synlett;2014-02-05

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