Product Information
- 2,2-Diallylpyrrolidine
- Pyrrolidine, 2,2-di-2-propen-1-yl-
Cephalotaxine, a pentacyclic nucleus, has been synthesized by means of an intramolecular cyclization. This reaction is accomplished with the use of a chloride ion and zinc chloride to produce the corresponding chlorides as intermediates. The sequence is accomplished by reacting these intermediates with 2,2-diallyl-pyrrolidine in the presence of sodium hydroxide. The synthesis is completed by metathesis using palladium on charcoal. In this way, cephalotaxine is obtained in the form of its diastereoisomer, which has been shown to be structurally identical to natural cephalotaxine.
Chemical properties
Technical inquiry about: 3D-QBA16297 2,2-Diallyl-pyrrolidine
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