Issue 2, 1998

Lithium enamides, β-diketiminates and 1,3-diazaallyls from the 1:1 insertion of an isonitrile into the Li–C bond of LiCH(SiMe3)2†‡

Abstract

The diverse behaviour of LiCHR2 A towards an isonitrile R′NC is unravelled; depending on reaction conditions and choice of R′, the product was an enamide Li[N(R′)C(R)[double bond, length half m-dash]C(H)R](tmen), a β-diketiminate L[upper bond 1 start]i[N(R′)C(R)C(H)C(R)N[upper bond 1 end](R′)], a 1,3-diazaallyl (with additionally PhCN) L[upper bond 1 start]i[N(Ph)C(R)N[upper bond 1 end]C(Ph)[double bond, length half m-dash]C(H)R](tmen) or a 1:1 adduct of A and L[upper bond 1 start]i[N(R′)C(R)C(H)C(R)N[upper bond 1 end](R′)](CNR′) (R′ = But), (R = SiMe3, tmen = Me2NCH2CH2NMe2 and R′ = But, Ph or C6H3Me2-2,6).

Article information

Article type
Paper

Chem. Commun., 1998, 201-202

Lithium enamides, β-diketiminates and 1,3-diazaallyls from the 1:1 insertion of an isonitrile into the Li–C bond of LiCH(SiMe3)2†‡

P. B. Hitchcock, M. F. Lappert and M. Layh, Chem. Commun., 1998, 201 DOI: 10.1039/A706709G

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