ICCAS OpenIR
Diastereoselective Synthesis of 3-Hydroxyindanones via N-Heterocyclic Carbene Catalyzed [4+1] Annulation of Phthalaldehyde and 1,2-Diactivated Michael Acceptors
Sun, Fang-Gang; Ye, Song
2011-04-01
Source PublicationSYNLETT
ISSN0936-5214
Issue7Pages:1005-1009
AbstractThe diastereoselective synthesis of 2,2-disubstituted-3-hydroxy-indanones was realized by the N-heterocyclic carbene catalyzed [4+1] annulation of phthalaldehyde and 1,2-diactivated Michael acceptors, which involves a tandem process of Stetter reaction, proton shift, and aldol reaction.
Keyword4+1] Annulation Tandem Reaction N-heterocyclic Carbenes Indanone Stetter Reaction
DOI10.1055/s-0030-1259707
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000289411900031
PublisherGEORG THIEME VERLAG KG
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Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/73228
Collection中国科学院化学研究所
Corresponding AuthorYe, Song
AffiliationChinese Acad Sci, Inst Chem, Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
Recommended Citation
GB/T 7714
Sun, Fang-Gang,Ye, Song. Diastereoselective Synthesis of 3-Hydroxyindanones via N-Heterocyclic Carbene Catalyzed [4+1] Annulation of Phthalaldehyde and 1,2-Diactivated Michael Acceptors[J]. SYNLETT,2011(7):1005-1009.
APA Sun, Fang-Gang,&Ye, Song.(2011).Diastereoselective Synthesis of 3-Hydroxyindanones via N-Heterocyclic Carbene Catalyzed [4+1] Annulation of Phthalaldehyde and 1,2-Diactivated Michael Acceptors.SYNLETT(7),1005-1009.
MLA Sun, Fang-Gang,et al."Diastereoselective Synthesis of 3-Hydroxyindanones via N-Heterocyclic Carbene Catalyzed [4+1] Annulation of Phthalaldehyde and 1,2-Diactivated Michael Acceptors".SYNLETT .7(2011):1005-1009.
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