ICCAS OpenIR
Highly enantioselective direct syn- and anti-aldol reactions of dihydroxyacetones catalyzed by chiral primary amine catalysts
Luo, Sanzhong1; Xu, Hui1; Zhang, Long2; Li, Jiuyuan1; Cheng, Jin-Pei1,2
2008-02-21
Source PublicationORGANIC LETTERS
ISSN1523-7060
Volume10Issue:4Pages:653-656
AbstractWe present herein simple primary-tertiary diamine-Bronsted acid conjugates that catalyze both syn- and anti-adol reactions of dihydroxyacetones (DHAs) with high diastereoselectivities and enantioselectivities. This type of organocatalysts functionally mimics all four DHA aldolases, namely L-fuculose-1-phosphate aldolase, D-tagatose-1,6-diphosphate aldolase, D-fructose-1,6-diphosphate aldolase, and L-rhamnulose-1-phosphate aldolase.
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000252989500033
PublisherAMER CHEMICAL SOC
Citation statistics
Cited Times:114[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/64176
Collection中国科学院化学研究所
Corresponding AuthorLuo, Sanzhong
Affiliation1.Chinese Acad Sci, Grad Sch, Inst Chem, Ctr Chem Biol,Beijing Natl Lab Mol Sci, Beijing 100080, Peoples R China
2.Nankai Univ, Dept Chem, State Key Lab Elemento Organ Chem, Tianjin 300071, Peoples R China
Recommended Citation
GB/T 7714
Luo, Sanzhong,Xu, Hui,Zhang, Long,et al. Highly enantioselective direct syn- and anti-aldol reactions of dihydroxyacetones catalyzed by chiral primary amine catalysts[J]. ORGANIC LETTERS,2008,10(4):653-656.
APA Luo, Sanzhong,Xu, Hui,Zhang, Long,Li, Jiuyuan,&Cheng, Jin-Pei.(2008).Highly enantioselective direct syn- and anti-aldol reactions of dihydroxyacetones catalyzed by chiral primary amine catalysts.ORGANIC LETTERS,10(4),653-656.
MLA Luo, Sanzhong,et al."Highly enantioselective direct syn- and anti-aldol reactions of dihydroxyacetones catalyzed by chiral primary amine catalysts".ORGANIC LETTERS 10.4(2008):653-656.
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