Abstract
The use of radical cyclisations allows direct access to a family of azaspirocyclic ketones, including compounds having the azaspiro[4.4]nonane, and azaspiro[5.5]undecane structures which are found in the alkaloids cephalotaxine and histrionicotoxin. © 1989.
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CITATION STYLE
APA
Middleton, D. S., Simpkins, N. S., & Terrett, N. K. (1989). Synthesis of N-protected spiroamines related to natural products using radical cyclisations. Tetrahedron Letters, 30(29), 3865–3868. https://doi.org/10.1016/S0040-4039(01)80679-1
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