1,3‐O‐Transposition or Trisubstituted Z‐Enol Ester? A Comparative Study of Reactions of Ynones-Reference-Cited by-同舟云学术

1,3‐O‐Transposition or Trisubstituted Z‐Enol Ester? A Comparative Study of Reactions of Ynones

Published:2019-05-08 Issue:11 Volume:14 Page:1941-1944
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Sun Tian‐Yu¹,Chen Kai²³^ORCID,Zhang Changyuan⁴,You Tingting¹,Yin Penggang¹^ORCID

Affiliation:

1. Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology of Ministry of EducationSchool of ChemistryBeihang University Beijing 100191 China

2. College of Materials Science and EngineeringCentral South University of Forestry and Technology Changsha 410004 China

3. Lab of Computational Chemistry and Drug DesignState Key Laboratory of Chemical OncogenomicsPeking University Shenzhen Graduate School Shenzhen 518055 China

4. College of Chemistry and Bio-EngineeringYichun University Yichun 336000 China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Natural Science Foundation of Hunan Province

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.201900315

Reference53 articles.

2. A Chiral N , N′ ‐Dioxide–Zn II Complex Catalyzes the Enantioselective [2+2] Cycloaddition of Alkynones with Cyclic Enol Silyl Ethers

3. A Chiral N , N′ ‐Dioxide–Zn II Complex Catalyzes the Enantioselective [2+2] Cycloaddition of Alkynones with Cyclic Enol Silyl Ethers

4. Silver(I)- or Copper(II)-Mediated Dearomatization of Aromatic Ynones: Direct Access to Spirocyclic Scaffolds

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