Catalytic Cyclopropanol Ring Opening for Divergent Syntheses of γ-Butyrolactones and δ-Ketoesters Containing All-Carbon Quaternary Centers-Reference-Cited by-同舟云学术

Catalytic Cyclopropanol Ring Opening for Divergent Syntheses of γ-Butyrolactones and δ-Ketoesters Containing All-Carbon Quaternary Centers

Published:2018-05-11 Issue:7 Volume:8 Page:5907-5914
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Ye Zhishi¹^ORCID,Cai Xinpei¹,Li Jiawei¹,Dai Mingji¹^ORCID

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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