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

Departament de Química

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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

Idioma original	Anglès
Pàgines (de-a)	335-336
Revista	Journal of Heterocyclic Chemistry
Volum	19
Número	2
DOIs	https://doi.org/10.1002/jhet.5570190223
Estat de la publicació	Publicada - 1 de gen. 1982

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10.1002/jhet.5570190223

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@article{a620624e94f74bf39062eba61594e0a8,

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",

year = "1982",

month = jan,

day = "1",

doi = "10.1002/jhet.5570190223",

language = "English",

volume = "19",

pages = "335--336",

journal = "Journal of Heterocyclic Chemistry",

issn = "0022-152X",

publisher = "John Wiley and Sons Inc.",

number = "2",

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TY - JOUR

T1 - Reactions between 4‐hydroxy‐6‐methyl‐2‐pyrone and aldehydes both in the absence and the presence of added thiols

AU - de March, P.

AU - Moreno‐Mañas, M.

AU - Pi, R.

AU - Trius, A.

PY - 1982/1/1

Y1 - 1982/1/1

N2 - 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

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

UR - https://www.scopus.com/pages/publications/84985240063

U2 - 10.1002/jhet.5570190223

DO - 10.1002/jhet.5570190223

M3 - Article

SN - 0022-152X

VL - 19

SP - 335

EP - 336

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 2

ER -

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

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