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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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. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c5ob01838b |