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Diastereoselective 1,3-dipolar cycloadditions with enantiopure azomethine ylids

DOI: 10.1016/S0040-4020(98)00638-3

Source and publish data:

Tetrahedron p. 10733 - 10752 (1998)

Update date:2022-07-30

Topics:

Authors:

Enders, DieterEnders, Dieter

Meyer, IlkaMeyer, Ilka

Runsink, JanRunsink, Jan

Raabe, GerhardRaabe, Gerhard

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Article abstract of DOI:10.1016/S0040-4020(98)00638-3

Secondary amines 2a-c, based on (4S,5S)-2,2-dimethyl-4-phenyl-1,3- dioxan-5-ylamine (1), were heated with a variety of aromatic aldehydes in chlorobenzene under reflux. The in situ generated 1,3-dipols were trapped with fumaric acid ester, fumaric acid ni

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Full text of DOI:10.1016/S0040-4020(98)00638-3

Products guided by the article

Product name:(1S,3S,3aS,6aR)-2-((4S,5S)-2,2-Dimethyl-4-phenyl-[1,3]dioxan-5-yl)-3-(4-methoxy-phenyl)-4,6-dioxo-5-phenyl-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid methyl ester

Cas No:214079-36-4

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