5,5-Disubstituted isoxazolidines undergo ring opening reaction, leading to tertiary allylic alcohols, by sequential treatment with trimethyl phosphate (TMP) and NaH. The reaction proceeds through sequence steps which involve an initial alkylation to isoxazolidinium intermediate, followed by ring expansion to tetrahydro-1,3-oxazine, further alkylation and a Hofmann-like elimination towards the final products promoted by NaH.
RING-OPENING OF ISOXAZOLIDINE NUCLEUS BY TRIMETHYL PHOSPHATE TREATMENT - FORMATION OF TERTIARY ALLYLIC ALCOHOLS VIA INTERMEDIATE 1,3-OXAZINIUM SALTS
SINDONA, Giovanni;
1993-01-01
Abstract
5,5-Disubstituted isoxazolidines undergo ring opening reaction, leading to tertiary allylic alcohols, by sequential treatment with trimethyl phosphate (TMP) and NaH. The reaction proceeds through sequence steps which involve an initial alkylation to isoxazolidinium intermediate, followed by ring expansion to tetrahydro-1,3-oxazine, further alkylation and a Hofmann-like elimination towards the final products promoted by NaH.File in questo prodotto:
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