A convenient access to allylic triflones with allenes and triflyl chloride in the presence of (EtO)2P(O)H-Reference-Cited by-同舟云学术

A convenient access to allylic triflones with allenes and triflyl chloride in the presence of (EtO)2P(O)H

Published:2019 Issue:51 Volume:55 Page:7343-7345
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Ni Jixiang¹²³⁴⁵,Jiang Yong⁶⁷⁸⁹^ORCID,An Zhenyu¹²³⁴⁵,Lan Jingfeng¹²³⁴⁵,Yan Rulong¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry

2. College of Chemistry and Chemical Engineering

3. Lanzhou University

4. Lanzhou

5. People's Republic of China

6. School of Chemistry and Chemical Engineering

7. Yangtze Normal University

8. Chongqing

9. China

Abstract

A simple method for the preparation of allylic triflones from allenes and triflyl chloride in the presence of (EtO)₂P(O)H has been developed.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC03096D

Reference46 articles.

1. Synthetic Methods for Compounds Having CF3–S Units on Carbon by Trifluoromethylation, Trifluoromethylthiolation, Triflylation, and Related Reactions

2. Einführung von Fluor und fluorhaltigen funktionellen Gruppen

3. Recent Progress in Direct Introduction of Fluorinated Groups on Alkenes and Alkynes by means of CH Bond Functionalization

4. The Many Roles for Fluorine in Medicinal Chemistry

5. Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design

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