Synthesis 2016; 48(16): 2619-2626
DOI: 10.1055/s-0035-1561958
special topic
© Georg Thieme Verlag Stuttgart · New York

Asymmetric Synthesis of Dipropionate Derivatives through Catalytic Hydrogenation of Enantioenriched E-Ketene Heterodimers

Shi Chen
a   Department of Chemistry, Oakland University, 2200 N. Squirrel Road, Rochester, MI 48309-4477, USA   Email: kerrigan@oakland.edu
,
Mukulesh Mondal
a   Department of Chemistry, Oakland University, 2200 N. Squirrel Road, Rochester, MI 48309-4477, USA   Email: kerrigan@oakland.edu
,
Ahmad A. Ibrahim
a   Department of Chemistry, Oakland University, 2200 N. Squirrel Road, Rochester, MI 48309-4477, USA   Email: kerrigan@oakland.edu
,
Kraig A. Wheeler
b   Department of Chemistry, Eastern Illinois University, 600 Lincoln Avenue, Charleston, IL 61920-3099, USA
,
Nessan J. Kerrigan*
a   Department of Chemistry, Oakland University, 2200 N. Squirrel Road, Rochester, MI 48309-4477, USA   Email: kerrigan@oakland.edu
› Author Affiliations
Further Information

Publication History

Received: 11 January 2016

Accepted after revision: 02 March 2016

Publication Date:
12 April 2016 (online)


Abstract

A highly diastereoselective approach to dipropionate derivatives through Pd/C-catalyzed hydrogenation of enantioenriched E-ketene heterodimers is described. Catalytic hydrogenation of the E-isomer of ketene heterodimer β-lactones (12 examples) provides access to syn,anti-β-lactones (dipropionate derivatives) bearing up to three stereogenic centers (dr up to 49:1), and with excellent transfer of chirality (ee up to >99%).

Supporting Information

 
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