A rapid and efficient one-pot method for the reduction of N-protected α-amino acids to chiral α-amino aldehydes using CDI/DIBAL-HElectronic supplementary information (ESI) available. See DOI: 10.1039/c5ob01838b

N -Protected amino acids can be easily converted into chiral α-amino aldehydes in a one-pot reaction by activation with CDI followed by reduction with DIBAL-H. This method delivers Boc-, Cbz- and Fmoc-protected amino aldehydes from proteinogenic amino acids in very good isolated yields and complete...

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Hauptverfasser: Ivkovic, Jakov, Lembacher-Fadum, Christian, Breinbauer, Rolf
Format: Artikel
Sprache:eng
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Zusammenfassung:N -Protected amino acids can be easily converted into chiral α-amino aldehydes in a one-pot reaction by activation with CDI followed by reduction with DIBAL-H. This method delivers Boc-, Cbz- and Fmoc-protected amino aldehydes from proteinogenic amino acids in very good isolated yields and complete stereointegrity. N -Protected α-amino acids can be easily converted directly into chiral α-amino aldehydes in a one-pot procedure by activation with CDI followed by reduction with DIBAL-H.
ISSN:1477-0520
1477-0539
DOI:10.1039/c5ob01838b