Highly Stereoselective Ring-Opening Addition of Terminal Acetylenes to Bicyclic Olefins Catalyzed by Nickel Complexes
Author:
Affiliation:
1. Department of Chemistry, Tsing Hua University, Hsinchu, Taiwan 300, Republic of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol025731d
Reference45 articles.
1. Nickel-catalyzed cocyclotrimerization of oxa- and azabenzonorbornadienes with alkynes: reaction with multiple synthetic applications
2. Stereoselective [2 + 2 + 2] cocyclotrimerization of oxa- and azabenzonorbornadienes † with alkynes catalyzed by nickel complexes: first transition metal-mediated synthesis of isobenzofuran and isoindole precursors
3. Nickel-Promoted First Ene−Diyne Cycloaddition Reaction on C60: Synthesis and Photochemistry of the Fullerene Derivatives
4. Nickel-Catalyzed [2+2] Cycloaddition of Alkynes with Activated Cyclic Alkenes: Synthesis and Novel Ring Expansion Studies of Cyclobutene Products
5. Nickel-Catalyzed Highly Regio- and Stereoselective Cyclization of Oxanorbornenes with Alkyl Propiolates: A Novel Method for the Synthesis of Benzocoumarin Derivatives
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