Chiral Lithium 2-Aminoalkoxides as Reagents for Enantioselective Michael Reaction

DOI: 10.1016/0957-4166(94)80103-7

Source and publish data:

Tetrahedron Asymmetry p. 1431 - 1432 (1994)

Update date:2022-08-16

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Authors:

Kumamoto, Takuya

Aoki, Shin

Nakajima, Makoto

Koga, Kenji

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Article abstract of DOI:10.1016/0957-4166(94)80103-7

Chiral lithium alkoxides were designed and applied to enantioselective Michael reaction of methyl phenylacetate and methyl acrylate to give the corresponding adduct in enantiomeric excess up to 84percent.The catalytic enantioselective Michael reaction is

Full text of DOI:10.1016/0957-4166(94)80103-7

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Product name:Pentanedioic acid, 2-phenyl-, dimethyl ester, (R)-

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