Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes-Reference-Cited by-同舟云学术

Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes

Published:2017 Issue:3 Volume:4 Page:358-368
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Xu Meng-Meng¹²³⁴,Wang Hai-Qing¹²³⁴,Wan Ying¹²³⁴,He Guofeng⁵⁶⁷⁴,Yan Jingjing⁵⁶⁷⁴,Zhang Shu⁵⁶⁷⁴,Wang Shu-Liang¹²³⁴,Shi Feng¹²³⁴

Affiliation:

1. School of Chemistry and Chemical Engineering

2. Jiangsu Normal University

3. Xuzhou

4. China

5. Department of Radiotherapy

6. The First Affiliated Hospital of Nanjing Medical University

7. Nanjing

Abstract

The first catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with enamines has been established.

Funder

National Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C6QO00549G

Reference62 articles.

1. 3-Acylated tetramic and tetronic acids as natural metal binders: myth or reality?

2. Tetramic and tetronic acids: An update on new derivatives and biological aspects

3. Spirodiclofen and Spiromesifen – Novel Acaricidal and Insecticidal Tetronic Acid Derivatives with a New Mode of Action

4. Juspurpurin, an Unusual Secolignan Glycoside from Justicia purpurea

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