SYNTHESIS OF OXACYCLIC CARBOXYLIC ESTERS THROUGH RING CLOSURE OF Α-ALKOXY ESTER FREE RADICALS

DOI: 10.1016/0040-4039(91)80366-E

Source and publish data:

Tetrahedron Letters p. 1491 - 1494 (1991)

Update date:2022-07-29

Topics:

Authors:

Lolkema, Lucie D. M.

Hiemstra, Henk

Ghouch, Al Ayachi Al

Speckamp, W. Nico

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Article abstract of DOI:10.1016/0040-4039(91)80366-E

Cyclizations of 1-methoxycarbonyl-2-oxa-5-hexenyl (and related) radical intermediates, generated from phenylthio precursors, proceed in good yields and mainly lead to substituted 2-tetrahydrofurancarboxylic esters.

Full text of DOI:10.1016/0040-4039(91)80366-E

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