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A novel reaction cascade leading to a spontaneous intramolecular dipolar cycloaddition through simultaneous generation of 1,3-dipole and dipolarophile
Authors:Nagabushanam Kalyanam  Keshav R Rapole  Ramanujam Rajendran  Muhammed Majeed
Institution:1. Sabinsa Corporation, 20 Lake Drive, East Windsor, NJ 08520, United States;2. Sami Labs Limited, Peenya Industrial Area, Bangalore 560058, India
Abstract:Ornithine methyl ester reacts with aromatic aldehydes to generate bis-Schiff bases, which depending on the structure of the aromatic aldehyde, further undergo an intramolecular cycloaddition through the transient formation of a reactive 1,3-dipole.
Keywords:Azomethine ylid  1  3-Dipolar addition  Cycloaddition  Dipolarophile  Stereoselective  Bis-Schiff bases of ornithine
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