THE SELECTIVE REDUCTIVE ACYLATION OF α-KETO IMINES

DOI: 10.1016/S0040-4039(01)91314-0

Source and publish data:

Tetrahedron Letters p. 3811 - 3812 (1981)

Update date:2022-08-04

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Authors:

Alper, Howard

Amaratunga, Shiyamaline

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Article abstract of DOI:10.1016/S0040-4039(01)91314-0

Reaction of α-keto imines with the in situ generated acetylcobalt tetracarbonyl occurs only at the carbon-nitrogen double bond to give β-keto amides.An unexpected by-product was formed in several instances.

Full text of DOI:10.1016/S0040-4039(01)91314-0

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