Stereoselective Synthesis of 3-Exo-Substituted 2-endo-Acyl-5-norborene Derivatives
Journal Article
The stereoselective addition of a variety of nucleophiles (ROH, RSH) to several 2-acylnorbornadienes provides an efficient synthesis of the title compounds. The allyl ethers derived from the addition of allyl alcohol are stable to many synthetic transformations and readily liberate the 3-exo alcohol on reductive cleavage. © 1974, American Chemical Society. All rights reserved.
Full Text
Duke Authors
Cited Authors
- Baldwin, SW; Tomesch, JC
Published Date
- August 1, 1974
Published In
Volume / Issue
- 39 / 16
Start / End Page
- 2382 - 2385
Electronic International Standard Serial Number (EISSN)
- 1520-6904
International Standard Serial Number (ISSN)
- 0022-3263
Digital Object Identifier (DOI)
- 10.1021/jo00930a011
Citation Source
- Scopus