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

Department of Chemistry

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

5 Citations (Scopus)

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 © 1991 Journal of Heterocyclic Chemistry

Original language	English
Pages (from-to)	2041-2043
Journal	Journal of Heterocyclic Chemistry
Volume	28
Issue number	8
DOIs	https://doi.org/10.1002/jhet.5570280842
Publication status	Published - 1 Jan 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",

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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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VL - 28

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EP - 2043

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 8

ER -

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

Abstract

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