Tf2NH-catalyzed formal [3 + 2] cycloaddition of oxadiazolones with ynamides: a simple access to aminoimidazoles-Reference-Cited by-同舟云学术

Tf2NH-catalyzed formal [3 + 2] cycloaddition of oxadiazolones with ynamides: a simple access to aminoimidazoles

Published:2017 Issue:16 Volume:15 Page:3413-3417
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhao Yingying¹²³⁴⁵,Hu Yancheng¹²³⁴,Li Xincheng¹²³⁴,Wan Boshun¹²³⁴^ORCID

Affiliation:

1. Dalian Institute of Chemical Physics

2. Chinese Academy of Sciences

3. Dalian 116023

4. China

5. University of Chinese Academy of Sciences

Abstract

We herein develop a formal [3 + 2] approach to access aminoimidazoles through the Tf₂NH-catalyzed cycloaddition of oxadiazolones with ynamides, in which oxadiazolones are first employed as the three-atom building units.

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/2017/OB/C7OB00701A

Reference41 articles.

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3. Rhodium-Catalyzed [2 + 2] Cycloaddition of Ynamides with Nitroalkenes

4. Computational ligand design in enantio- and diastereoselective ynamide [5+2] cycloisomerization

5. Enantioselective Ficini Reaction: Ruthenium/PNNP-Catalyzed [2+2] Cycloaddition of Ynamides with Cyclic Enones

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