Synthesis of highly functionalised enantiopure bicyclo[3.2.1]- octane systems from carvone.
نویسندگان
چکیده
The commercially available monoterpene carvone has been efficiently converted into the tricyclo[3.2.1.0(2.7)]octane and bicyclo[3.2.1]octane systems characteristic of some biologically active compounds. The sequence used for this transformation involves as key features an intramolecular Diels-Alder reaction of a 5-vinyl-1,3-cyclohexadiene and a cyclopropane ring opening.
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ورودعنوان ژورنال:
- Molecules
دوره 9 5 شماره
صفحات -
تاریخ انتشار 2004