ICCAS OpenIR
Reaction of ketene aminals with aryl isothiocyanates - A simple route to isothiazole compounds
Zhao, MX; Wang, MX; Huang, ZT
2001
Source PublicationACTA CHIMICA SINICA
ISSN0567-7351
Volume59Issue:10Pages:1763-1768
AbstractCyclic and acyclic ketene aminals with different electron withdrawing groups reacted with aryl isothiocyanates to give the corresponding alpha - carbon adducts in high yield which underwent oxidative cyclization with bromine to afford isothiazole compounds in moderate yield.
KeywordCyclic And aCyclic Ketene Aminals Aryl Isothiocyanate Isothiazole Compound
Indexed BySCI
Language英语
WOS IDWOS:000171884400042
PublisherSCIENCE PRESS
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Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/77342
Collection中国科学院化学研究所
Corresponding AuthorZhao, MX
AffiliationChinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Zhao, MX,Wang, MX,Huang, ZT. Reaction of ketene aminals with aryl isothiocyanates - A simple route to isothiazole compounds[J]. ACTA CHIMICA SINICA,2001,59(10):1763-1768.
APA Zhao, MX,Wang, MX,&Huang, ZT.(2001).Reaction of ketene aminals with aryl isothiocyanates - A simple route to isothiazole compounds.ACTA CHIMICA SINICA,59(10),1763-1768.
MLA Zhao, MX,et al."Reaction of ketene aminals with aryl isothiocyanates - A simple route to isothiazole compounds".ACTA CHIMICA SINICA 59.10(2001):1763-1768.
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