Synergic transformation of an ethylenediamine to a lithium 1,3-diaza-2-zincacyclopentene via an alkyllithium/bis(alkyl)zinc mixture

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Abstract

Deadly duo: Four bonds in total, two N-H and two C-H bonds, have been cleaved from a neutral secondary diamine through the cooperative effects of a lithium alkyl-zinc bisalkyl coalition aided by N,N,N',N'- tetramethylethylenediamine (TMEDA) to generate a dianionic diazaethene (see scheme). © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Campbell, R., García-Álvarez, P., Kennedy, A. R., & Mulvey, R. E. (2010). Synergic transformation of an ethylenediamine to a lithium 1,3-diaza-2-zincacyclopentene via an alkyllithium/bis(alkyl)zinc mixture. Chemistry - A European Journal, 16(33), 9964–9968. https://doi.org/10.1002/chem.201001314

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