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Decarboxylative Julia- Kocienski gem- Difluoro- Olefination of 2-Pyridinyl Sulfonyldifluoroacetate

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成果类型:
期刊论文
作者:
Wang, Xiao-Ping;Lin, Jin-Hong;Xiao, Ji-Chang*;Zheng, Xing
通讯作者:
Xiao, Ji-Chang
作者机构:
[Lin, Jin-Hong; Xiao, Ji-Chang; Wang, Xiao-Ping] Chinese Acad Sci, Key Lab Organofluorine Chem, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China.
[Wang, Xiao-Ping; Zheng, Xing] Univ South China, Inst Pharm & Pharmacol, Hengyang 421001, Hunan, Peoples R China.
[Xiao, Ji-Chang] Chinese Acad Sci, Key Lab Organofluorine Chem, Shanghai Inst Organ Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China.
通讯机构:
[Xiao, Ji-Chang] C
Chinese Acad Sci, Key Lab Organofluorine Chem, Shanghai Inst Organ Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China.
语种:
英文
关键词:
Fluorine;Decarboxylation;Sulfur;Olefination;Aldehydes
期刊:
European Journal of Organic Chemistry
ISSN:
1434-193X
年:
2014
卷:
2014
期:
5
页码:
928-932
基金类别:
National Natural Science Foundation of China (NSFC)National Natural Science Foundation of China (NSFC) [21032006, 21172240]; 973 Program of ChinaNational Basic Research Program of China [2012CBA01200]; Chinese Academy of SciencesChinese Academy of Sciences
机构署名:
本校为其他机构
院系归属:
药学与生物科学学院
摘要:
The decarboxylation of potassium 2-pyridinyl sulfonyldifluoroacetate and its subsequent reaction with aldehydes was found to be an efficient approach for the Julia-Kocienski reaction under mild conditions to give gem-difluoro olefins in moderate to excellent yields. Owing to its high stability in the pure state and its easy decarboxylation in polar solvents, potassium 2-pyridinyl sulfonyldifluoroacetate is expected to be an efficient gem-difluoro-olefination reagent. The decarboxylation of potassium 2-pyridinyl sulfonyldifluoroacetate and its s...

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