Applications of the β-Azidonation Reaction to Organic Synthesis. α,β-Enones, Conjugate Addition, and γ-Lactam Annulation
Author:
Affiliation:
1. Contribution from the Department of Chemistry and Biochemistry, University of Texas at Austin, Austin, Texas 78712
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja9829564
Reference56 articles.
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2. New trialkylsilyl enol ether chemistry: new regiospecific methodology for the synthesis of α,β-unsaturated cyclic ketones
3. New trialkylsilyl enol ether chemistry. Conjugate additions without the enone
4. New trialkylsilyl enol ether chemistry: intramolecular [2 + 2] cyclizations of .beta.-amido triisopropylsilyl enol ethers
5. Synthesis of the Antitumor Alkaloid (+)-Pancratistatin Using the β-Azidonation Reaction via a Prochiral 4-Arylcyclohexanone Derivative
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