Synthesis of D-erythrose and D-threose derived nitrones and cycloadditions to styrene

DOI: 10.1016/S0040-4020(99)00512-8

Source and publish data:

Tetrahedron p. 9501 - 9514 (1999)

Update date:2022-08-05

Topics:

Authors:

Kuban, Juraj

Blanarikova, Iva

Fisera, L'ubor

Jaroskova, Libuse

Fengler-Veith, Marion

Jaeger, Volker

Kozisek, Jozef

Humpa, Otakar

Pronayova, Nad'a

Langer, Vratislav

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Article abstract of DOI:10.1016/S0040-4020(99)00512-8

The new nitrones derived from cyclic acetals of D-erythrose (2a-c) and D-threose (8) react with styrene to afford the corresponding 3,5- disubstituted diastereomeric isoxazolidines 3-6 and 9-12. The stereoselectivity was dependent on the steric hindrance

Full text of DOI:10.1016/S0040-4020(99)00512-8

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