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  • Aldehyde selective Wacker oxidations of phthalimide protected allylic amines: a new catalytic route to beta3-amino acids.

Aldehyde selective Wacker oxidations of phthalimide protected allylic amines: a new catalytic route to beta3-amino acids.

Journal of the American Chemical Society (2009-07-09)
Barbara Weiner, Alejandro Baeza, Thomas Jerphagnon, Ben L Feringa
ABSTRACT

A new method for the synthesis of beta(3)-amino acids is presented. Phthalimide protected allylic amines are oxidized under Wacker conditions selectively to aldehydes using PdCl(2) and CuCl or Pd(MeCN)(2)Cl(NO(2)) and CuCl(2) as complementary catalyst systems. The aldehydes are produced in excellent yields and exhibit a large substrate scope. Beta-amino acids and alcohols are synthesized by oxidation or reduction and subsequent deprotection.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Phthalimide potassium salt, purum, ≥99.0% (NT)
Sigma-Aldrich
Phthalimide potassium salt, 98%
Sigma-Aldrich
Phthalimide, ≥99%