Stereoselective Synthesis of Isomeric Functionalized 1,3-Dienes from Cyclobutenones
Author:
Affiliation:
1. Department of Synthetic Chemistry and Biological Chemistry Kyoto University, Yoshida, Kyoto 606-8501, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja010639i
Reference12 articles.
1. Electronic Control of Stereoselectivities of Electrocyclic Reactions of Cyclobutenes: A Triumph of Theory in the Prediction of Organic Reactions
2. A Silyl Substituent Can Dictate a Concerted Electrocyclic Pathway: Inward Torquoselectivity in the Ring Opening of 3-Silyl-1-cyclobutene
3. Geminal Bond Participation in the Electrocyclic Reactions: Torquoselectivities of Silyl and Trimethylsilyl Derivatives of Cyclobutene, Iminocyclobutene, and Cyclobutenone
4. A general method for the reductive dechlorination of 4,4-dichlorocyclobutenones
5. A regiocontrolled annulation approach to highly substituted aromatic compounds
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