Issue 16, 1997
From the journal:

Chemical Communications

Bis(N-piperidyl)carbene and its slow dimerisation to tetrakis(N-piperidyl)ethene

Roger W. Alder  and  Michael E. Blake  

Abstract

An unhindered bis(sec-amino)carbene can be generated by deprotonation of an amidinium ion with lithium diisopropylamide, and undergoes remarkably slow dimerisation to the corresponding tetraaminoethene.

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Article information

DOI
https://doi.org/10.1039/A703610H
Article type
Paper

Chem. Commun., 1997, 1513-1514

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Bis(N-piperidyl)carbene and its slow dimerisation to tetrakis(N-piperidyl)ethene

R. W. Alder and M. E. Blake, Chem. Commun., 1997, 1513 DOI: 10.1039/A703610H

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