Phosphine-Mediated Sequential Staudinger/Aza-Michael Addition of Azides with Unsaturated Ketones to Synthesize β-Amino Substituted Ketones

doi:10.6023/cjoc201906005

Chinese Journal of Organic Chemistry ›› 2019, Vol. 39 ›› Issue (8): 2157-2165.DOI: 10.6023/cjoc201906005 Previous Articles Next Articles

Special Issue: 陈茹玉先生诞辰100周年；元素有机化学合辑2018-2019

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叔膦介导的叠氮化合物与不饱和酮的连续Staudinger/Aza-Michael加成反应合成β-氨基取代酮类化合物

丛甜甜^a, 王华敏^a, 刘媛媛^a, 吴海虹^a, 张俊良^a,b

a 华东师范大学化学与分子工程学院上海市绿色化学与化工过程绿色化重点实验室上海 200062;
b 复旦大学化学系上海 200438

收稿日期:2019-06-06 修回日期:2019-07-09 发布日期:2019-07-17
通讯作者: 刘媛媛, 吴海虹, 张俊良 E-mail:yyliu@chem.ecnu.edu.cn;hhwu@chem.ecnu.edu.cn;junliangzhang@fudan.edu.cn
基金资助:
国家自然科学基金（No.21871088）、上海市教育发展基金会和上海市教育委员会“晨光计划”（No.16CG22）、中央高校基本科研业务费专项资金（No.21871088）资助项目.

Phosphine-Mediated Sequential Staudinger/Aza-Michael Addition of Azides with Unsaturated Ketones to Synthesize β-Amino Substituted Ketones

Cong Tiantian^a, Wang Huamin^a, Liu Yuanyuan^a, Wu Haihong^a, Zhang Junliang^a,b

a Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062;
b Department of Chemistry, Fudan University, Shanghai 200438

Received:2019-06-06 Revised:2019-07-09 Published:2019-07-17
Contact: 10.6023/cjoc201906005 E-mail:yyliu@chem.ecnu.edu.cn;hhwu@chem.ecnu.edu.cn;junliangzhang@fudan.edu.cn
Supported by:
Project supported by the National Natural Science Foundation of China (No. 21871088), the Chenguang Program supported by Shanghai Education Development Foundation and Shanghai Municipal Education Commission (No. 16CG22), and the Fundamental Research Funds for the Central Universities (No. 21871088).

1. Phosphine-Mediated Sequential Staudinger/Aza-Michael Addition of Azides with Unsaturated Ketones to Synthesize β-Amino Substituted Ketones.PDF(4346KB)

Abstract

A phosphine-mediated Staudinger/Aza-Michael addition of azides with trifluoromethyl substituted α,β-unsaturated ketones was developed, giving hydroamination products in medium to good yields (up to 96%). The hydroamination products could be prepared on gram scale and a wide range of substrates are tolerated under the optimized reaction conditions (30 examples). ³¹P NMR experiments indicate that this reaction was initiated by Staudinger reaction of azide with phosphine.

Key words: phosphines, Staudinger reaction, aza-Michael addition, azides, hydroamination, alkenes

Cite this article

Cong Tiantian, Wang Huamin, Liu Yuanyuan, Wu Haihong, Zhang Junliang. Phosphine-Mediated Sequential Staudinger/Aza-Michael Addition of Azides with Unsaturated Ketones to Synthesize β-Amino Substituted Ketones[J]. Chinese Journal of Organic Chemistry, 2019, 39(8): 2157-2165.

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叔膦介导的叠氮化合物与不饱和酮的连续Staudinger/Aza-Michael加成反应合成β-氨基取代酮类化合物

Phosphine-Mediated Sequential Staudinger/Aza-Michael Addition of Azides with Unsaturated Ketones to Synthesize β-Amino Substituted Ketones

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