Highly Diastereoselective Diels−Alder Reactions of Baylis−Hillman Adducts
Author:
Affiliation:
1. School of Chemistry, University of Bristol, Cantock's Close, BS8 1TS Bristol, UK
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol050584f
Reference9 articles.
1. New Strategies for the Development of an Asymmetric Version of the Baylis–Hillman Reaction
2. Correlation between pKa and Reactivity of Quinuclidine-Based Catalysts in the Baylis−Hillman Reaction: Discovery of Quinuclidine as Optimum Catalyst Leading to Substantial Enhancement of Scope
3. Recent Advances in the Baylis−Hillman Reaction and Applications
4. A Chiral Acrylate Equivalent for Metal-Free Diels−Alder Reactions: endo-2-Acryloylisoborneol
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