Abstract
Reaction of 1 equivalent of N-“-acetyl-cis-4-azido-L-proline with 1 equivalent of an aldehyde and a catalytic amount of Pd-C under an H2 atmosphere cleanly and efficiently yields the corresponding N-“-acetylcis- 4-(N-γ-alkylamino)-L-proline derivative.
Keywords: aminoproline, reductive amination, azide, aldehyde, secondary amine
Letters in Organic Chemistry
Title: A Simple, High Yield Route to cis-4-(N-Alkylamino)-L-Prolines
Volume: 2 Issue: 1
Author(s): Timothy P. Curran, Kevin A. Marques and Segufta I. Bilimoria
Affiliation:
Keywords: aminoproline, reductive amination, azide, aldehyde, secondary amine
Abstract: Reaction of 1 equivalent of N-“-acetyl-cis-4-azido-L-proline with 1 equivalent of an aldehyde and a catalytic amount of Pd-C under an H2 atmosphere cleanly and efficiently yields the corresponding N-“-acetylcis- 4-(N-γ-alkylamino)-L-proline derivative.
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Cite this article as:
Curran P. Timothy, Marques A. Kevin and Bilimoria I. Segufta, A Simple, High Yield Route to cis-4-(N-Alkylamino)-L-Prolines, Letters in Organic Chemistry 2005; 2 (1) . https://dx.doi.org/10.2174/1570178053400063
DOI https://dx.doi.org/10.2174/1570178053400063 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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