南方科技大学知识苑(SUSTech KC): Difluorocarbene-enabled access to 1,3-oxazin-6-ones from enamides

题名	Difluorocarbene-enabled access to 1,3-oxazin-6-ones from enamides
作者	Wang, Shuai 1; Li, Xin 1; Jin, Shengnan 1; Liu, Kang 1; Dong, Cong 1; Su, Jianke 1; Song, Qiuling 1,2,3,4,5
通讯作者	Song, Qiuling
发表日期	2022
DOI	10.1039/d1qo01899j
发表期刊	Organic Chemistry Frontiers 影响因子和分区
ISSN	2052-4129
卷号	9页码:1282-1287
摘要	1,3-Oxazin-6-ones as important structural scaffolds widely exist in many bioactive or therapeutic agents. The development of straightforward synthetic approaches to access 1,3-oxazin-6-ones is highly desirable for studying their fundamental properties and applications. Herein, we report an efficient and general strategy for the construction of 1,3-oxazin-6-ones with high efficiency and chemoselectivity. Instead of using CO as a C1 source, difluorocarbene was introduced as a carbonyl provider. This method features readily available starting materials and valuable products, good functional group tolerance, and simple operation.
相关链接	[来源记录]
收录类别	SCI ; EI
语种	英语
学校署名	通讯
资助项目	National Natural Science Foundation of China[21931013] ; Guangdong Provincial Key Laboratory of Catalysis[2020B121201002]
WOS研究方向	Chemistry
WOS类目	Chemistry, Organic
WOS记录号	WOS:000746123800001
出版者	ROYAL SOC CHEMISTRY
EI入藏号	20221011770297
来源库	Web of Science
引用统计	被引频次[WOS]：9
成果类型	期刊论文
条目标识符	http://sustech.caswiz.com/handle/2SGJ60CL/273328
专题	南方科技大学
作者单位	1.Huaqiao Univ, Inst Next Generat Matter Transformat, Coll Mat Sci Engn, 668 Jimei Blvd, Xiamen 361021, Fujian, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China 3.Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China 4.Southern Univ Sci & Technol, Guangdong Prov Key Lab Catalysis, Shenzhen 518055, Guangdong, Peoples R China 5.Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Henan, Peoples R China
通讯作者单位	南方科技大学
推荐引用方式 GB/T 7714	Wang, Shuai,Li, Xin,Jin, Shengnan,et al. Difluorocarbene-enabled access to 1,3-oxazin-6-ones from enamides[J]. Organic Chemistry Frontiers,2022,9:1282-1287.
APA	Wang, Shuai.,Li, Xin.,Jin, Shengnan.,Liu, Kang.,Dong, Cong.,...&Song, Qiuling.(2022).Difluorocarbene-enabled access to 1,3-oxazin-6-ones from enamides.Organic Chemistry Frontiers,9,1282-1287.
MLA	Wang, Shuai,et al."Difluorocarbene-enabled access to 1,3-oxazin-6-ones from enamides".Organic Chemistry Frontiers 9(2022):1282-1287.