An unusual reaction at C‐3 of 4‐methoxy‐6‐methyl‐2‐pyrone

M. Moreno‐Mañas; R. Pleixats

doi:10.1002/jhet.5570280842

An unusual reaction at C‐3 of 4‐methoxy‐6‐methyl‐2‐pyrone

M. Moreno‐Mañas, R. Pleixats

Departamento de Química

Producción científica: Contribución a una revista › Artículo › Investigación › revisión exhaustiva

5 Citas (Scopus)

Resumen

Triacetic acid lactone methyl ether, 4, can be lithiated at C‐3 under kinetically controlled conditions. Further reaction with (E)‐2‐methyl‐3‐(4‐nitrophenyl)propenal results in an unusual condensation at C‐3. Copyright © 1991 Journal of Heterocyclic Chemistry

Idioma original	Inglés
Páginas (desde-hasta)	2041-2043
Publicación	Journal of Heterocyclic Chemistry
Volumen	28
N.º	8
DOI	https://doi.org/10.1002/jhet.5570280842
Estado	Publicada - 1 ene 1991

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title = "An unusual reaction at C‐3 of 4‐methoxy‐6‐methyl‐2‐pyrone",

abstract = "Triacetic acid lactone methyl ether, 4, can be lithiated at C‐3 under kinetically controlled conditions. Further reaction with (E)‐2‐methyl‐3‐(4‐nitrophenyl)propenal results in an unusual condensation at C‐3. Copyright {\textcopyright} 1991 Journal of Heterocyclic Chemistry",

author = "M. Moreno‐Ma{\~n}as and R. Pleixats",

year = "1991",

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AU - Pleixats, R.

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N2 - Triacetic acid lactone methyl ether, 4, can be lithiated at C‐3 under kinetically controlled conditions. Further reaction with (E)‐2‐methyl‐3‐(4‐nitrophenyl)propenal results in an unusual condensation at C‐3. Copyright © 1991 Journal of Heterocyclic Chemistry

AB - Triacetic acid lactone methyl ether, 4, can be lithiated at C‐3 under kinetically controlled conditions. Further reaction with (E)‐2‐methyl‐3‐(4‐nitrophenyl)propenal results in an unusual condensation at C‐3. Copyright © 1991 Journal of Heterocyclic Chemistry

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DO - 10.1002/jhet.5570280842

M3 - Article

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JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

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An unusual reaction at C‐3 of 4‐methoxy‐6‐methyl‐2‐pyrone

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