Issue 24, 1980
From the journal:

Journal of the Chemical Society, Chemical Communications

Synthesis of a conjugated triene diamine [1,2-bis(β-dimethylaminovinyl)cyclopentene] through the isomerization of an αω-diaminonadiyne

Roland Epsztein  and  Bernard Herman  

Abstract

The diacetylenic diamine (3a) rearranges instantaneously and quantitatively, via its lithium derivative, to the triene diamine (4a).

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Article information

DOI
https://doi.org/10.1039/C39800001250
Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 1250-1251

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Synthesis of a conjugated triene diamine [1,2-bis(β-dimethylaminovinyl)cyclopentene] through the isomerization of an αω-diaminonadiyne

R. Epsztein and B. Herman, J. Chem. Soc., Chem. Commun., 1980, 1250 DOI: 10.1039/C39800001250

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