Catalytic Cyclopropanol Ring Opening for Divergent Syntheses of γ-Butyrolactones and δ-Ketoesters Containing All-Carbon Quaternary Centers
Author:
Affiliation:
1. Department of Chemistry, Center for Cancer Research, and Institute for Drug Discovery, Purdue University, West Lafayette, Indiana 47907, United States
Funder
Division of Chemistry
American Chemical Society Petroleum Research Fund
Eli Lilly and Company
Publisher
American Chemical Society (ACS)
Subject
Catalysis,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acscatal.8b00711
Reference85 articles.
1. Rearrangement of 1-(1-Alkynyl)cyclopropanols to 2-Cyclopentenones via Their Hexacarbonyldicobalt Complexes. A New Use of Alkyne−Co2(CO)6 Complexes in Organic Synthesis
2. Gold(I)-Catalyzed Ring Expansion of Cyclopropanols and Cyclobutanols
3. Stereoselective, Dual-Mode Ruthenium-Catalyzed Ring Expansion of Alkynylcyclopropanols
4. Gold(I)-Catalyzed Enantioselective Ring Expansion of Allenylcyclopropanols
5. Dual Visible Light Photoredox and Gold-Catalyzed Arylative Ring Expansion
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