Breaking aziridines to construct morpholines with a gold(i)-catalyzed tandem ring-opening and cycloisomerization reaction-Reference-Cited by-同舟云学术

Breaking aziridines to construct morpholines with a gold(i)-catalyzed tandem ring-opening and cycloisomerization reaction

Published:2016 Issue:46 Volume:14 Page:10973-10980
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhang Shuyao¹²³⁴⁵,Shan Chuan¹²³⁴⁵,Zhang Shuai¹²³⁴⁵,Yuan Luye¹²³⁴⁵,Wang Jianwu¹²³⁴⁵,Tung Chen-Ho¹²³⁴⁵,Xing Ling-Bao¹²³⁴⁵,Xu Zhenghu¹²³⁴⁵^ORCID

Affiliation:

1. Key Lab for Colloid and Interface Chemistry of Education Ministry

2. School of chemistry and Chemical Engineering

3. Shandong University

4. Jinan 250100

5. People's Republic of China

Abstract

A convenient synthetic method for the construction of morpholine derivatives from easily available aziridines and propargyl alcohols has been successfully developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB02284G

Reference93 articles.

1. Synthesis and anti-inflammatory activity of phthalimide derivatives, designed as new thalidomide analogues

2. Synthesis of novel compounds containing morpholine and 5(4H)-oxazolone rings as potent tyrosinase inhibitors

3. Antihyperlipidemic morpholine derivatives with antioxidant activity: An investigation of the aromatic substitution

4. Synthesis and glycosidase inhibitory profiles of functionalised morpholines and oxazepanes

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