Gold(I)‐Catalyzed Ring Expansion of Alkynylcyclopropyl Allyl Ethers to Construct Tetrasubstituted Methylenecyclobutanones: A Mechanistic Investigation about the Character of Catalytic Amount of Water-Reference-Cited by-同舟云学术

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Gold(I)‐Catalyzed Ring Expansion of Alkynylcyclopropyl Allyl Ethers to Construct Tetrasubstituted Methylenecyclobutanones: A Mechanistic Investigation about the Character of Catalytic Amount of Water

Published:2019-04-04 Issue:10 Volume:361 Page:2321-2328
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Zang Wenqing¹,Wang Lei¹,Wei Yin¹,Shi Min¹,Guo Yinlong¹

Affiliation:

1. State Key Laboratory of Organometallic ChemistryCenter for Excellence in Molecular SynthesisUniversity of Chinese Academy of SciencesShanghai Institute of Organic ChemistryChinese Academy of Sciences 345 Lingling Road Shanghai 200032 People's Republic of China

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201900053

Reference96 articles.

1.

2. Carben‐Umlagerungen, X. 2‐Vinylcyclobutyliden

3. Ketene-diene [4 + 2] cycloaddition products via cation radical initiated Diels-Alder reaction or vinylcyclobutanone rearrangement

4. Reassignment of stereochemistry of the 3-ethoxy-2-methyl-2-vinylcyclobutanones

5. On the mechanism of rhodium-catalyzed [6+2] cycloaddition of 2-vinylcyclobutanones and alkenes

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2. Alkynyl cyclopropanes in organic synthesis;Russian Chemical Bulletin;2024-01

3. Electrophilic functionalization of N-substituted vicinal alkynyl(amino)cyclopropanes via selective lithiation;Russian Chemical Bulletin;2023-08

4. Molecular Rearrangements;Organic Reaction Mechanisms Series;2023-01-20

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