Citation: Zhang Yahui, Liu Yang, Miao Jiankang, Hao Wenyan. Copper-Catalyzed Cascade Bicyclization of o-Alkenylphenyl Isothiocyanates with Sodium Azide Leading to the 5H-Benzo[d]tetrazolo[5, 1-b] [1, 3]thiazines[J]. Chinese Journal of Organic Chemistry, ;2020, 40(8): 2426-2432. doi: 10.6023/cjoc201912036 shu

Copper-Catalyzed Cascade Bicyclization of o-Alkenylphenyl Isothiocyanates with Sodium Azide Leading to the 5H-Benzo[d]tetrazolo[5, 1-b] [1, 3]thiazines

Key Laboratory of Functional Small Organic Molecules, Ministry of Education, College of Chemistry & Chemical Engineering, Jiangxi Normal University, Nanchang 330022

Corresponding author: Hao Wenyan, wenyanhao@jxnu.edu.cn
Received Date: 25 December 2019
Revised Date: 12 May 2020
Available Online: 25 May 2020
Fund Project: the Research Fund of Jiangxi provincial Education Department GJJ160285the Natural Science Foundation of Jiangxi Province 2018BAB203006Project supported by the National Natural Science Foundation of China (No. 21762023), the Natural Science Foundation of Jiangxi Province (No. 2018BAB203006) and the Research Fund of Jiangxi provincial Education Department (No. GJJ160285)National Natural Science Foundation of China 21762023

Figures(4)

A simple and efficient method for the preparation of 5H-benzo[d]tetrazolo[5, 1-b] ^{[1, 3]}thiazines has been developed. The transformation involved the copper(I)-catalyzed cascade bicyclization of o-alkenylphenyl isothiocyanates with sodium azide to afford corresponding products in moderate to good yields. This present strategy provides an effective way to construct small molecular N-, and S-heterocycles.
- copper-catalysis,
- cascade bicyclization,
- 5H-benzo[d]tetrazolo[5, 1-b] [1, 3]thiazine,
- o-alkenylphenyl isothiocyanate
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