Hydroximate as a synthetically useful functional group part II: Synthesis of (±)-oxo-parabenzlactone

DOI: 10.1248/cpb.44.1285

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1285 - 1287 (1996)

Update date:2022-08-04

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Authors:

Miyata, Okiko

Nishiguchi, Atsuko

Ninomiya, Ichiya

Naito, Takeaki

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Article abstract of DOI:10.1248/cpb.44.1285

A stereoselective route to (±)-oxo-parabenzlactone has been developed by the combination of thiyl radical addition-cyclization of dienylhydroximate and subsequent conversion of the resulting cyclic hydroximate to lactone.

Full text of DOI:10.1248/cpb.44.1285

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