Synlett 2016; 27(09): 1397-1402
DOI: 10.1055/s-0035-1561566
letter
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Novel Imidazopyrrolo-Fused Isoxazole Derivatives through Acid-Mediated Intramolecular 1,3-Dipolar Cycloaddition

Yin Xu
a   Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. of China   Email: lizhong@ecust.edu.cn
,
Fukai Wang
a   Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. of China   Email: lizhong@ecust.edu.cn
,
Jiling Li
a   Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. of China   Email: lizhong@ecust.edu.cn
,
Xusheng Shao
a   Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. of China   Email: lizhong@ecust.edu.cn
,
Xiaoyong Xu
a   Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. of China   Email: lizhong@ecust.edu.cn
,
Zhong Li*
a   Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. of China   Email: lizhong@ecust.edu.cn
b   Shanghai Collaborative Innovation Center for Biomanufacturing Technology, 130 Meilong Road, Shanghai 200237, P. R. of China
› Author Affiliations
Further Information

Publication History

Received: 24 November 2015

Accepted after revision: 15 January 2016

Publication Date:
04 March 2016 (online)


Preview

Abstract

A facile approach to 4H-imidazo[1′,2′:1,2]pyrrolo[3,4-c]isoxazole derivatives was developed via intramolecular 1,3-dipolar cycloaddition catalyzed by p-toluenesulfonic acid. The method allows the convenient construction of novel tricyclic isoxazoles under mild reaction conditions and moderate yields.

Supporting Information