Issue 26, 2018
From the journal:

Organic & Biomolecular Chemistry

Pd-Catalyzed diastereoselective [3 + 2] cycloaddition of vinylcyclopropanes with sulfamate-derived cyclic imines†

Qijun Wang,a   Chang Wang,a   Wangyu Shi,a   Yumei Xiao*a  and  Hongchao Guo ORCID logo *a  

* Corresponding authors

a Department of Applied Chemistry, China Agricultural University, Beijing 100193, China
E-mail: hchguo@cau.edu.cn, xiaoyumei@cau.edu.cn

Abstract

The palladium-catalyzed diastereoselective [3 + 2] cycloaddition reaction of vinylcyclopropanes with sulfamate-derived cyclic imines worked efficiently under mild reaction conditions, providing 2,3-dihydrobenzo[e]pyrrolo[1,2-c][1,2,3]oxathiazine 5,5-dioxide derivatives in good to excellent yields.

Graphical abstract: Pd-Catalyzed diastereoselective [3 + 2] cycloaddition of vinylcyclopropanes with sulfamate-derived cyclic imines

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Article information

DOI
https://doi.org/10.1039/C8OB01231H
Article type
Paper
Submitted
25 May 2018
Accepted
16 Jun 2018
First published
19 Jun 2018

Org. Biomol. Chem., 2018,16, 4881-4887

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Pd-Catalyzed diastereoselective [3 + 2] cycloaddition of vinylcyclopropanes with sulfamate-derived cyclic imines

Q. Wang, C. Wang, W. Shi, Y. Xiao and H. Guo, Org. Biomol. Chem., 2018, 16, 4881 DOI: 10.1039/C8OB01231H

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