Llwytho...

A general, enantioselective synthesis of β- and γ-fluoroamines

In this Letter, we describe a short, high yielding protocol for the enantioselective (87–96% ee) and general synthesis of β-fluoroamines and previously difficult to access γ-fluoroamines from commercial aldehydes via organocatalysis.

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: O’Reilly, Matthew C., Lindsley, Craig W.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2013
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3769685/
https://ncbi.nlm.nih.gov/pubmed/24039308
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2013.04.116
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