β-Amino esters via the Reformatsky reaction: Restraining effects of the ortho-methoxyphenyl substituent

DOI: 10.1016/S0040-4039(99)00248-8

Source and publish data:

Tetrahedron Letters p. 2457 - 2460 (1999)

Update date:2022-08-25

Topics:

Authors:

Adrian Jr., James C.

Barkin, Julia L.

Hassib, Lamyaa

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Article abstract of DOI:10.1016/S0040-4039(99)00248-8

β-Amino esters are, in most cases, the only products of the Reformatsky reaction in CH₂Cl₂ between (methoxycarbonyl)methyl zinc bromide (prepared in-situ) and imines prepared from either an aryl or alkyl aldehyde and o- anisdine (Sch

Full text of DOI:10.1016/S0040-4039(99)00248-8

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