A useful α,α '-annulation reaction of enamines Journal Article


Authors: Frontier, A. J.; Danishefsky, S. J.; Koppel, G. A.; Meng, D.
Article Title: A useful α,α '-annulation reaction of enamines
Abstract: The reactions of a series of enamines generated from a range of cyclic ketones with chloromethyl and iodomethyl vinyl ketone have been studied. The principal products are bridged ring diketones. The four carbon bridge, bearing a 2-oxobutyl function, spans the alpha and alpha' carbons of the original cyclanone. Presumptive evidence as to the pathway of this novel one step bridging annulation is provided. (C) 1998 Elsevier Science Ltd. All rights reserved.
Keywords: addition reactions; annulation; cp-225,917; cyclisation; cp-263,114
Journal Title: Tetrahedron
Volume: 54
Issue: 42
ISSN: 0040-4020
Publisher: Elsevier Inc.  
Date Published: 1998-10-01
Start Page: 12721
End Page: 12736
Language: English
ACCESSION: WOS:000076179100007
DOI: 10.1016/s0040-4020(98)00788-1
PROVIDER: wos
Notes: Article -- Source: Wos
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  1. Dongfang   Meng
    17 Meng