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Solvent-Free and Stereoselective Synthesis of C-Glycosides by Michael-Type Addition of Enamino Esters to 2-Nitro-D-glucal
Zhang, Ti1,2; Yu, Chu-Yi1; Huang, Zhi-Tang1; Jia, Yue-Mei1
2010-09-01
Source PublicationSYNLETT
ISSN0936-5214
Issue14Pages:2174-2178
AbstractMichael-type addition of enamino esters to 3,4,6-tri-O-benzyl-2-nitro-D-glucal under solvent-free conditions formed C-glycosides in excellent yields with high stereoselectivity. Reduction of the nitro group afforded the corresponding bicyclic 2-amino C-glycosides.
KeywordSolvent-free C-glycosides Michael-type Addition
DOI10.1055/s-0030-1258498
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000281197300029
PublisherGEORG THIEME VERLAG KG
Citation statistics
Cited Times:13[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/71224
Collection中国科学院化学研究所
Corresponding AuthorYu, Chu-Yi
Affiliation1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
Recommended Citation
GB/T 7714
Zhang, Ti,Yu, Chu-Yi,Huang, Zhi-Tang,et al. Solvent-Free and Stereoselective Synthesis of C-Glycosides by Michael-Type Addition of Enamino Esters to 2-Nitro-D-glucal[J]. SYNLETT,2010(14):2174-2178.
APA Zhang, Ti,Yu, Chu-Yi,Huang, Zhi-Tang,&Jia, Yue-Mei.(2010).Solvent-Free and Stereoselective Synthesis of C-Glycosides by Michael-Type Addition of Enamino Esters to 2-Nitro-D-glucal.SYNLETT(14),2174-2178.
MLA Zhang, Ti,et al."Solvent-Free and Stereoselective Synthesis of C-Glycosides by Michael-Type Addition of Enamino Esters to 2-Nitro-D-glucal".SYNLETT .14(2010):2174-2178.
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