Brønsted acid mediated intramolecular cyclopropane ring expansion/[4 + 2]-cycloaddition-Reference-Cited by-同舟云学术

Brønsted acid mediated intramolecular cyclopropane ring expansion/[4 + 2]-cycloaddition

Published:2019 Issue:47 Volume:17 Page:10004-10008
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Li Jian¹²³⁴⁵^ORCID,Zhu Shangrong¹²³⁴⁵,Xu Qiuneng¹²³⁴⁵,Liu Li¹²³⁴⁵,Yan Shenghu¹²³⁴⁵

Affiliation:

1. Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology

2. School of Pharmaceutical Engineering & Life Sciences

3. Changzhou University

4. Changzhou

5. China

Abstract

A cascade reaction of 3-hydroxy-2-phenylisoindolin-1-one and cyclopropyl ketone has been developed via BrØnsted acid-promoted ring-opening/intramolecular cross-cycloaddition/[4 + 2]-cycloaddition process.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB02379H

Reference55 articles.

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4. Heterocycles from cyclopropanes: applications in natural product synthesis

5. Donor−Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis

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