Functionalisation in position 3 of 3,5-dichloro-2H-1,4-oxazin-2-ones

DOI: 10.1016/S0040-4039(00)79064-2

Source and publish data:

Tetrahedron Letters p. 2713 - 2716 (1992)

Update date:2022-08-04

Topics:

Authors:

Van Aken

Meerpoel

Hoornaert

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Article abstract of DOI:10.1016/S0040-4039(00)79064-2

Electrophilic catalysis is shown to give selective substitution of the imidoyl chloride group in 3,5-dichloro-2H-1,4-oxazin-2-ones, avoiding competitive reactions of the nucleophile with the lactone function.With other nucleophiles (SCN^-, CH View More

Full text of DOI:10.1016/S0040-4039(00)79064-2

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