W(CO)5(L)-Catalyzed Tandem Intramolecular Cyclopropanation/Cope Rearrangement for the Stereoselective Construction of Bicyclo[5.3.0]decane Framework
Author:
Affiliation:
1. Department of Chemistry, Tokyo Institute of Technology, O-okayama, Meguro-ku, Tokyo 152-8551, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja0671924
Reference13 articles.
1. W(CO)5·THF-Catalyzed Endo-Selective Cyclization of ω-Acetylenic Silyl Enol Ethers
2. A Novel Reaction for Annulation onto α,β-Unsaturated Ketones: W(CO)5·L Promoted Exo- and Endo-Selective Cyclizations of ω-Acetylenic Silyl Enol Ethers Prepared by 1,4-Addition of Propargyl Malonate to Enones
3. W(CO)5-Amine Catalyzed Exo- and Endo-Selective Cyclizations of ω-Alkynyl Silyl Enol Ethers: A Highly Useful Method for the Construction of Polycyclic Compounds
4. An Efficient Method for Cyclopentene Annulation onto α,β-Unsaturated Ketones: W(CO)5(L)-Catalyzed 5-Endo-Dig Cyclization of 6-Siloxy-5-en-1-ynes
5. The Mechanistic Puzzle of Transition-Metal-Catalyzed Skeletal Rearrangements of Enynes
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