Remarkable solvent effect on the enantioface selectivity in the Diels- Alder reaction catalyzed by an aluminum complex of a newly prepared chiral menthol derivative

DOI: 10.1016/S0040-4039(97)10202-7

Source and publish data:

Tetrahedron Letters p. 8231 - 8232 (1997)

Update date:2022-08-02

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Authors:

Naraku, Go

Hori, Kiyoto

Ito, Yoshio N.

Katsuki, Tsutomu

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Article abstract of DOI:10.1016/S0040-4039(97)10202-7

Reversal of enantioface selectivity was observed by merely switching the solvent from CH₂Cl₂ (enantiomer ratio of the adduct = 91:9) to THF (14:86) in the asymmetric Diels-Alder reaction catalyzed by the aluminum complex of a newly p

Full text of DOI:10.1016/S0040-4039(97)10202-7

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