Reactions between 4‐hydroxy‐6‐methyl‐2‐pyrone and aldehydes both in the absence and the presence of added thiols

P. de March; M. Moreno‐Mañas; R. Pi; A. Trius

doi:10.1002/jhet.5570190223

Reactions between 4‐hydroxy‐6‐methyl‐2‐pyrone and aldehydes both in the absence and the presence of added thiols

P. de March, M. Moreno‐Mañas, R. Pi, A. Trius

Department of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

35 Citations (Scopus)

Abstract

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. Copyright © 1982 Journal of Heterocyclic Chemistry

Original language	English
Pages (from-to)	335-336
Journal	Journal of Heterocyclic Chemistry
Volume	19
Issue number	2
DOIs	https://doi.org/10.1002/jhet.5570190223
Publication status	Published - 1 Jan 1982

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title = "Reactions between 4‐hydroxy‐6‐methyl‐2‐pyrone and aldehydes both in the absence and the presence of added thiols",

abstract = "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. Copyright {\textcopyright} 1982 Journal of Heterocyclic Chemistry",

author = "{de March}, P. and M. Moreno‐Ma{\~n}as and R. Pi and A. Trius",

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AU - Pi, R.

AU - Trius, A.

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AB - 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. Copyright © 1982 Journal of Heterocyclic Chemistry

U2 - 10.1002/jhet.5570190223

DO - 10.1002/jhet.5570190223

M3 - Article

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JO - Journal of Heterocyclic Chemistry

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