2014
DOI: 10.1002/chin.201408148
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Asymmetric Formation of tert‐Alkylamines from Serinols by a Dual Function Catalyst.

Abstract: Catalyst. -A series of enantiopure oxazolidinones (III), useful tert.-alkylamine building blocks, is prepared in an one-pot manner by intramolecular desymmetrization of serinols (I) by a copper-catalyzed cyclization and a subsequent kinetic resolution of enantiomerically enriched hydroxymethyl-oxazolidinone intermediates (75-80% e.e.) by a benzoylation. -(YOU, Y. S.; KIM, T. W.; KANG*, S. H.; Chem. Commun. (Cambridge) 49 (2013) 83, 9669-9671, http://dx.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?