HUSCAP logo Hokkaido Univ. logo

Hokkaido University Collection of Scholarly and Academic Papers >
Graduate School of Science / Faculty of Science >
Peer-reviewed Journal Articles, etc >

Efficient Preparation of β-Branched γ,δ-Unsaturated Esters through Copper-Catalyzed Allylic Alkylation of Ketene Silyl Acetal

Files in This Item:
Syn44-9_1304-1307.pdf214.33 kBPDFView/Open
Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/52716

Title: Efficient Preparation of β-Branched γ,δ-Unsaturated Esters through Copper-Catalyzed Allylic Alkylation of Ketene Silyl Acetal
Authors: Li, Dong Browse this author
Ohmiya, Hirohisa Browse this author
Sawamura, Masaya Browse this author →KAKEN DB
Keywords: γ,δ-unsaturated esters
copper
allylic alkylation
ketene silyl acetal
regioselectivity
Issue Date: May-2012
Publisher: Georg Thieme Verlag
Journal Title: Synthesis
Volume: 44
Issue: 9
Start Page: 1304
End Page: 1307
Publisher DOI: 10.1055/s-0031-1289712
Abstract: Copper-catalyzed allylic alkylation of ketene silyl acetals proceeded with excellent γ-E-selectivity. Efficient α-to-γ chirality transfer with anti-selectivity occurred in the reaction of enantioenriched secondary allylic phosphates, affording enantioenriched β-branched γ,δ-unsaturated esters. The reaction was readily scalable and highly reliable in terms of product yield and stereoselectivities.
Rights: © 2012 Georg Thieme Verlag
Type: article (author version)
URI: http://hdl.handle.net/2115/52716
Appears in Collections:理学院・理学研究院 (Graduate School of Science / Faculty of Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 澤村 正也

Export metadata:

OAI-PMH ( junii2 , jpcoar_1.0 )

MathJax is now OFF:


 

 - Hokkaido University