6533b7d6fe1ef96bd1266f12
RESEARCH PRODUCT
ChemInform Abstract: Carbohydrates as Chiral Templates: Diastereoselective Synthesis of N- Glycosyl-N-homoallylamines and β-Amino Acids from Imines.
Sabine LaschatHorst Kunzsubject
chemistry.chemical_classificationchemistry.chemical_compoundTemplatechemistryStereochemistryDiastereomerGlycosylGeneral MedicineChirality (chemistry)Asymmetric inductionAmino aciddescription
Complexing properties and chirality of carbohydrates were utilized in diastereoselective reactions of 0-pivaloylated N-galactosylimines with allylsilanes and -stannaries. With dyltrimethylsilane in the presence of SnCl4, imines 2 of aromatic and heteroaromatic aldehydes were converted to homdylamines 3, giving ratios of diastereomers higher than 7:1. No addition products derived from α-anomeric aromatic imines were formed. Aliphatic homdylamines 3 were synthesized by using allyltributylstannane in the presence of SnCl4. Both α- and β-anomeric aliphatic imines reacted with the allylstannane. They gave the same ratio of diastereomers and showed the same sense of asymmetric induction.
year | journal | country | edition | language |
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2010-08-22 | ChemInform |