LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
N-Bromosuccinimide as an oxidant for the transition-metal-free synthesis of 2-aminobenzoxazoles from benzoxazoles and secondary amines
DepartmentOSSO国家重点实验室
Wang XE(王晓娥)1,2; Xu DQ(徐大乾)1; Miao CX(苗成霞)1; Zhang QH(张巧红)1; Sun W(孙伟)1; Sun W(孙伟)
2014
Source PublicationOrganic and Biomolecular Chemistry
ISSN1477-0520
Volume12Issue:19Pages:3108-3113
Abstract

A facile and transition-metal-free method was developed through merging the ring opening of benzoxazoles with secondary amines and N-bromosuccinimide (NBS) mediated oxidative cyclization toward the synthesis of 2-aminobenzoxazoles. NBS was selected as a powerful oxidant in the oxidative cyclization of ring-opening amidines to provide the desirable 2-aminobenzoxazoles in excellent yields (up to 94%).

Subject Area物理化学与绿色催化
DOI10.1039/c4ob00386a
Funding Organizationthe National Natural Science Foundation of China (21103207;21103206;21133011)
Indexed BySCI
If3.562
Language英语
Funding Project生物与仿生催化课题组
compositor第一作者单位
Citation statistics
Cited Times:33[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/21268
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorSun W(孙伟)
Affiliation1.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
Recommended Citation
GB/T 7714
Wang XE,Xu DQ,Miao CX,et al. N-Bromosuccinimide as an oxidant for the transition-metal-free synthesis of 2-aminobenzoxazoles from benzoxazoles and secondary amines[J]. Organic and Biomolecular Chemistry,2014,12(19):3108-3113.
APA Wang XE,Xu DQ,Miao CX,Zhang QH,Sun W,&孙伟.(2014).N-Bromosuccinimide as an oxidant for the transition-metal-free synthesis of 2-aminobenzoxazoles from benzoxazoles and secondary amines.Organic and Biomolecular Chemistry,12(19),3108-3113.
MLA Wang XE,et al."N-Bromosuccinimide as an oxidant for the transition-metal-free synthesis of 2-aminobenzoxazoles from benzoxazoles and secondary amines".Organic and Biomolecular Chemistry 12.19(2014):3108-3113.
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