The preparation of (α-alkylidene)tetrahydrofurans by tungsten catalyzed decarboxylation of aldol precursors

Tomoya Tanzawa; Jeffrey Schwartz

doi:10.1016/S0040-4039(00)61775-6

The preparation of (α-alkylidene)tetrahydrofurans by tungsten catalyzed decarboxylation of aldol precursors

Tomoya Tanzawa
, Jeffrey Schwartz

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

6 Scopus citations

Abstract

A series of substituted (α-alkylidene)tetrahydrofurans was prepared by tungsten catalyzed reaction of substituted hydroxyfuroic acids. These reactions likely involve β-lactone intermediates which decarboxylate under the reaction conditions, and rates for olefin synthesis correlated with donor properties of substituents at C(4).

Original language	English (US)
Pages (from-to)	6783-6786
Number of pages	4
Journal	Tetrahedron Letters
Volume	33
Issue number	45
DOIs	https://doi.org/10.1016/S0040-4039(00)61775-6
State	Published - Nov 3 1992

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)61775-6

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title = "The preparation of (α-alkylidene)tetrahydrofurans by tungsten catalyzed decarboxylation of aldol precursors",

abstract = "A series of substituted (α-alkylidene)tetrahydrofurans was prepared by tungsten catalyzed reaction of substituted hydroxyfuroic acids. These reactions likely involve β-lactone intermediates which decarboxylate under the reaction conditions, and rates for olefin synthesis correlated with donor properties of substituents at C(4).",

author = "Tomoya Tanzawa and Jeffrey Schwartz",

year = "1992",

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doi = "10.1016/S0040-4039(00)61775-6",

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pages = "6783--6786",

journal = "Tetrahedron Letters",

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T1 - The preparation of (α-alkylidene)tetrahydrofurans by tungsten catalyzed decarboxylation of aldol precursors

AU - Tanzawa, Tomoya

AU - Schwartz, Jeffrey

PY - 1992/11/3

Y1 - 1992/11/3

N2 - A series of substituted (α-alkylidene)tetrahydrofurans was prepared by tungsten catalyzed reaction of substituted hydroxyfuroic acids. These reactions likely involve β-lactone intermediates which decarboxylate under the reaction conditions, and rates for olefin synthesis correlated with donor properties of substituents at C(4).

AB - A series of substituted (α-alkylidene)tetrahydrofurans was prepared by tungsten catalyzed reaction of substituted hydroxyfuroic acids. These reactions likely involve β-lactone intermediates which decarboxylate under the reaction conditions, and rates for olefin synthesis correlated with donor properties of substituents at C(4).

UR - https://www.scopus.com/pages/publications/0026490350

UR - https://www.scopus.com/pages/publications/0026490350#tab=citedBy

U2 - 10.1016/S0040-4039(00)61775-6

DO - 10.1016/S0040-4039(00)61775-6

M3 - Article

AN - SCOPUS:0026490350

SN - 0040-4039

VL - 33

SP - 6783

EP - 6786

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 45

ER -

The preparation of (α-alkylidene)tetrahydrofurans by tungsten catalyzed decarboxylation of aldol precursors

Abstract

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