9‐Membered Carbocycle Formation: Development of Distinct Friedel–Crafts Cyclizations and Application to a Scalable Total Synthesis of (±)‐Caraphenol A1. (23rd February 2014)

• Record Type: Journal Article
• Authors: Wright, Nathan E.; Snyder, Scott A.
• Is Part Of: Angewandte Chemie. Volume 126:Number 13(2014)
• Page Start: 3477
• Page End: 3481
• Publication Date: 2014-02-23
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201311299
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Explorations into a series of different approaches for 9‐membered carbocycle formation have afforded the first reported example of a 9‐<italic>exo</italic>‐dig ring closure via a Au^III‐promoted reaction between an alkyne and an aryl ring as well as several additional, unique Friedel–Crafts‐type cyclizations. Analyses of the factors leading to the success of these transformations are provided, with the application of one of the developed 9‐membered ring closures affording an efficient and scalable synthesis of the bioactive resveratrol trimer caraphenol A. That synthesis proceeded with an average yield of 89 % per step (7.8 % overall yield) and has provided access to more than 600 mg of the target molecule.</p> </abstract>