文献类型：期刊文献

英文题名：Direct synthesis of N-substituted 1,3-oxazolidines via a hetero-domino Petasis borono-Mannich reaction of 1,2-amino alcohols, formaldehyde, and organoboronic acids

作者：Zheng, Yiting[1];Sun, Lu[1];Wang, Jiayi[1];Song, Gonghua[1]

机构：[1]East China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R China

年份：2019

卷号：55

期号：7

起止页码：648

外文期刊名：CHEMISTRY OF HETEROCYCLIC COMPOUNDS

收录：;EI(收录号：20242616311601);WOS:【SCI-EXPANDED(收录号:WOS:000483688800012)，CCR-EXPANDED(收录号:WOS:000483688800012)】；

基金：Financial support for this work from the National Key R&D Program (grant No. 2017YFD0200504), the National Natural Science Foundation of China (grant No. 21572060), the Shanghai Key Laboratory of Catalysis Technology for Polyolefins (LCTP-201301), and the Fundamental Research Funds for the Central Universities is gratefully acknowledged.

语种：英文

外文关键词：1,3-oxazolidines; cyclization; hetero-domino reaction; Petasis borono-Mannich reaction; three-component reaction

摘要：A simple and convenient approach to the synthesis of N-substituted 1,3-oxazolidines via a hetero-domino Petasis borono-Mannich reaction of 1,2-amino alcohols, formaldehyde, and organoboronic acids has been reported. The transformation provides an effective and complementary pathway toward 1,3-oxazolidine derivatives.