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A practical gold-catalyzed route to 4-substituted oxazolidin-2-ones from N-Boc propargylamines

Authors
Lee, Eun-SunYeom, Hyun-SukHwang, Ji-HyunShin, Seunghoon
Issue Date
Jul-2007
Publisher
WILEY-V C H VERLAG GMBH
Keywords
gold; oxazolidinones; 1,3-allylic interactions; isomerization
Citation
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, v.2007, no.21, pp.3503 - 3507
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume
2007
Number
21
Start Page
3503
End Page
3507
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179894
DOI
10.1002/ejoc.200700210
ISSN
1434-193X
Abstract
Au-I-catalyzed cyclization of N-Boc propargylamines into 4-alkylidene oxazolidin-2-ones is described. This modular approach provides access to a variety of nonproteogenic 4-substituted oxazolidinones that are important in asymmetric synthesis and biological applications. The current flexible route is characterized by low catalyst loading, mild conditions, and operational simplicity.
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