Issue 16, 1997

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

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.

Article information

Article type
Paper

Chem. Commun., 1997, 1513-1514

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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