Enantioselective Syntheses of Tremulenediol A and Tremulenolide A
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, Texas 78712
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol051945u
Reference11 articles.
1. The tremulanes, a new group of sesquiterpenes from the aspen rotting fungus Phellinus tremulae
2. Total Synthesis of (±)-Tremulenolide A and (±)-Tremulenediol A via a Stereoselective Cyclopropanation/Cope Rearrangement Annulation Strategy
3. Transition Metal-Catalyzed [5+2] Cycloadditions with Substituted Cyclopropanes: First Studies of Regio- and Stereoselectivity
4. Enantioselective Intramolecular Cyclopropanations of Allylic and Homoallylic Diazoacetates and Diazoacetamides Using Chiral Dirhodium(II) Carboxamide Catalysts
5. [Rh(CO)2Cl]2-Catalyzed Domino Reactions Involving Allylic Substitution and Subsequent Carbocyclization Reactions
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