Unexpected reduction of N-hydroxyphthalimides to phthalimides - orthogonal reduction of functionalized N-hydroxyphthalimides.
A chemoselective redn. of N-hydroxyphthalimides to phthalimides under mild conditions has been discovered. It involves reaction of an N-hydroxyimide with bis(pinacolato)diboron in the presence of a base. Other easily reducible functional groups, such as iodo, nitro, or azido groups are unaffected. Alternatively, such functional groups may be selectively reduced without affecting the N-hydroxyimide moiety using a set of classical conditions. [on SciFinder(R)]
Références
- Titre
- Unexpected reduction of N-hydroxyphthalimides to phthalimides - orthogonal reduction of functionalized N-hydroxyphthalimides.
- Type de publication
- Article de revue
- Année de publication
- 2010
- Auteurs
- Jacq, Jerome, Berthiol Florian, Einhorn Cathy, and Einhorn Jacques
- Revue
- Synlett
- Pagination
- 2263–2266
- ISSN
- 0936-5214
Soumis le 12 avril 2018