Reactions between 4-hydroxy-6-methyl-2-pyrone and aldehydes both in the absence and the presence of added thiols
JOURNAL OF HETEROCYCLIC CHEMISTRY(1982)
摘要
Aldehydes react with 4-hydroxy-6-methyl-2-pyrone, 2, under Knoevenagel conditions to afford very elec-trophilic intermediates, which can be trapped by more 2 or thiols to give dilactones 3 or monolactones 4.
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