Bronsted acid-catalyzed aza Diels-Alder reaction of Danishefsky's diene with aldimine generated in situ from aldehyde and amine in aqueous media

DOI: 10.1016/S0040-4039(99)01630-5

Source and publish data:

Tetrahedron Letters p. 7831 - 7834 (1999)

Update date:2022-08-16

Topics:

Authors:

Akiyama, Takahiko

Takaya, Jun

Kagoshima, Hirotaka

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Article abstract of DOI:10.1016/S0040-4039(99)01630-5

Three-component aza Diels-Alder reaction, starting from aldehyde, aniline, and Danishefsky's diene, took place smoothly under the influence of HBF₄ in aqueous media to afford dihydro-4-pyridone derivatives in high yields.

Full text of DOI:10.1016/S0040-4039(99)01630-5

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