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Communication | Special issue | Vol 47, No. 1, 1998, pp.107-110
Published online, 1st January, 1970
DOI: 10.3987/COM-97-S(N)36
Diastereoselective Indium-promoted Addition of Functionalized Allyl Bromides to N-Benzyl-2,3-azetidinedione under Aqueous Conditions

Leo A. Paquette* and Methvin B. Isaac

*Evans Chemical Laboratories, The Ohio State University, 120 W. 18th Avenue, Columbus, Ohio 43210, U.S.A.


The stereodifferentiation attending the coupling of geometrically stable allylindium reagents to a 2,3-azetidinedione has been assessed and found to operate at a synthetically useful level in most cases.