Stereoselective Intramolecular Aminocarbonylation of 3-Hydroxypent-4-enylamides Catalyzed by Palladium

DOI: 10.1016/S0040-4039(00)88935-2

Source and publish data:

Tetrahedron Letters p. 4479 - 4482 (1985)

Update date:2022-08-04

Topics: Palladium Catalyzed Stereoselective Intramolecular Aminocarbonylation

Authors:

Tamaru, Yoshinao

Kobayashi, Takuji

Kawamura, Shin-ichi

Ochiai, Hirofumi

Yoshida, Zen-ichi

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Article abstract of DOI:10.1016/S0040-4039(00)88935-2

The urethanes and tosamides of 3-Hydroxypent-4-enylamine and its C₁-C₄ substituted derivatives undergo the palladium catalyzed intramolecular aminocarbonylation (0.1 equiv of PdCl₂, 3.0 equiv of CuCl2, 3.0 equiv of NaOAc i

Full text of DOI:10.1016/S0040-4039(00)88935-2

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