Intramolecular Carbolithiation as a Route to a Sterically Congested Cyclopentene: Synthesis of the Longtailed Mealybug Pheromone
Author:
Affiliation:
1. Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269-3060, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo4002118
Reference17 articles.
1. Sex Pheromone of the Longtailed Mealybug: A New Class of Monoterpene Structure
2. Synthesis of the Pheromone of the Longtailed Mealybug, a Sterically Congested, Irregular Monoterpenoid
3. Improved Synthesis of the Pheromone of the Longtailed Mealybug
4. Convenient general method for the preparation of primary alkyllithiums by lithium-iodine exchange
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