Abstract
The synthesis of the hexahydronaphthalene moiety (6b) of (+)-mevinolin (1) has been achieved in 10 steps using an intramolecular Diels-Alder reaction of an alkenylallene to set up four of the chiral centers and the diene unit of (6b). © 1983.
Cite
CITATION STYLE
APA
Deutsch, E. A., & Snider, B. B. (1983). Synthesis of the hexahydronaphthalene moiety of (+)-mevinolin. Tetrahedron Letters, 24(35), 3701–3704. https://doi.org/10.1016/S0040-4039(00)94513-1
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free