Studies on structurally simple α,β-butenolides. VII. An easy entry to γ-thiomethyl- and γ-aminomethyl-α, β-butenolides

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Abstract

The reaction of the dilithium salt of phenylselenoacetic acid with a variety of glycidyl substrates yields 5-heteromethyl-3-phenylseleno-tetrahydrofuran-2-ones. Selective oxidation of the selenium atom allows the preparation of 5-thiomethyl- and 5-aminomethyl-2-(5H)-furanones. © 1987.
Original languageEnglish
Pages (from-to)1881-1886
JournalTetrahedron
Volume43
Issue number8
DOIs
Publication statusPublished - 1 Jan 1987

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