A simple and efficient method for the synthesis of novel spiropyrrolidines has been accomplished by regioselective 1,3-dipolar cycloaddition reactions of an azomethine ylide generated by thermalring opening of cis-1-cyclohexyl-2-phenyl-3-benzoyl aziridine with various (E)-3-arylidene-4-chromanones.
β¦ LIBER β¦
ChemInform Abstract: Synthesis of Spiropyrrolidines: 1,3-Dipolar Cycloaddition Reactions of an Azomethine Ylide to Unusual Dipolarophiles; a Molecular Orbital Study of the Cycloaddition Reaction.
β Scribed by A. Amal Raj; R. Raghunathan; E. J. P. Malar
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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