Amine-Catalyzed Direct Aldol Reactions of Hydroxy- and Dihydroxyacetone: Biomimetic Synthesis of Carbohydrates

被引:22
|
作者
Popik, Oskar [1 ]
Pasternak-Soder, Monika [2 ]
Lesniak, Katarzyna [2 ]
Jawiczuk, Magdalena [1 ]
Gorecki, Marcin [1 ]
Frelek, Jadwiga [1 ]
Mlynarski, Jacek [1 ,2 ]
机构
[1] Polish Acad Sci, Inst Organ Chem, PL-01224 Warsaw, Poland
[2] Jagiellonian Univ, Fac Chem, PL-30060 Krakow, Poland
来源
JOURNAL OF ORGANIC CHEMISTRY | 2014年 / 79卷 / 12期
关键词
WATER-COMPATIBLE ORGANOCATALYSTS; DE-NOVO SYNTHESIS; DIRECT SYN-ALDOL; ASYMMETRIC-SYNTHESIS; ANTI-ALDOL; CONFIGURATIONAL ASSIGNMENT; ABSOLUTE-CONFIGURATION; AUXILIARY CHROMOPHORES; VIC-DIOLS; ACID;
D O I
10.1021/jo500860g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This article presents comprehensive studies on the application of primary, secondary, and tertiary amines as efficient organocatalysts for the de novo synthesis of ketoses and deoxyketoses. Mimicking the actions of aldolase enzymes, the synthesis of selected carbohydrates was accomplished in aqueous media by using proline- and serine-based organocatalysts. The presented methodology also provides direct access to unnatural L-carbohydrates from the (S)-glyceraldehyde precursor. Determination of the absolute configuration of all obtained sugars was feasible using a methodology consisting of concerted ECD and VCD spectroscopy.
引用
收藏
页码:5728 / 5739
页数:12
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