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Synthesis of 2-Azetidiniminium Salts. 1. Diastereoselectivity in Keteniminium Triflate/Imine Cycloadditions

โœ Scribed by Barbaro, Gaetano; Battaglia, Arturo; Bruno, Cristiana; Giorgianni, Patrizia; Guerrini, Andrea


Book ID
121201116
Publisher
American Chemical Society
Year
1996
Tongue
English
Weight
261 KB
Volume
61
Category
Article
ISSN
0022-3263

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โœ Pil-Jong Shim; Hee-Doo Kim ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 244 KB

Optically active bicyclo[4.2.0]octan-7-ones were synthesized by stereoselective intramolecular [2+2] cycloaddition of alkene-keteniminium salt derived from L-glutamic acid, based on 1,3-asymmelric induction. Synthetic application toward (+)-gibberellic acid key intermediate was also described.