Preparation of and attack by nucleophiles on 2, 5-norbornadione

Abstract

Several oxidative approaches to 2,5-norbornadione have been tried resulting in an improved preparative route to the compound. 2,5-Norbornadione has also been reacted with phenylmagnesium-bromide, p-tolymagnesium bromide, o-tolylmagnesium bromide, and 1-napthylmagnesium bromide. The resulting 2,5-diols have been characterized and shown to be the endo, endo alcohols.

Degree

MS

College and Department

Physical and Mathematical Sciences; Chemistry and Biochemistry

Rights

http://lib.byu.edu/about/copyright/

Date Submitted

1975-04-01

Document Type

Thesis

Handle

http://hdl.lib.byu.edu/1877/Letd697

Keywords

norbornadione

Language

English

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