Au-Catalyzed tandem intermolecular hydroalkoxylation/Claisen rearrangement between allylic alcohols and chloroalkynes-Reference-Cited by-同舟云学术

Au-Catalyzed tandem intermolecular hydroalkoxylation/Claisen rearrangement between allylic alcohols and chloroalkynes

Published:2019 Issue:18 Volume:17 Page:4435-4439
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Liu Congrong¹²³⁴^ORCID,Xu Jin⁵⁶⁷³⁴,Ding Lianghui¹²³⁴,Zhang Haiyun¹²³⁴,Xue Yunbo¹²³⁴,Yang Fulai⁸⁹³¹⁰

Affiliation:

1. School of Environment Engineering

2. Nanjing Institute of Technology

3. Nanjing

4. China

5. Key Laboratory of Watershed Geographic Sciences

6. Nanjing Institute of Geography and Limnology

7. Chinese Academy of Sciences

8. Department of Organic Chemistry

9. China Pharmaceutical University

10. P. R. China

Abstract

An efficient protocol for the synthesis of γ,δ-unsaturated α-chloroketones has been developed via Au-catalyzed tandem intermolecular hydroalkoxylation/Claisen rearrangement.

Funder

National Natural Science Foundation of China

Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences

Nanjing Institute of Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00151D

Reference62 articles.

1. Über Umlagerung von Phenol‐allyläthern in C ‐Allyl‐phenole

2. Über die Umlagerung von Phenolallyläthern in die isomeren Allylphenole

3. New aspects of the Ireland and related Claisen rearrangements

4. Claisen Rearrangement over the Past Nine Decades

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