Synthesis of N-protected spiroamines related to natural products using radical cyclisations

27Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free