A plausible chemical analogy for biosynthesis of 2-arylbenzofuran of isoflavonoid origin and its application to synthesis of vignafuran

DOI: 10.1016/S0040-4039(96)02276-9

Source and publish data:

Tetrahedron Letters p. 259 - 262 (1997)

Update date:2022-08-02

Topics: Synthesis NMR spectroscopy Catalyst Stereochemistry Organic chemistry Reagent Biosynthesis: Authors:

Kinoshita, Takeshi

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Article abstract of DOI:10.1016/S0040-4039(96)02276-9

Treatment of 2-hydroxy-isoflav-3-ene with acid afforded 2-arylbenzofuran in good yield, and a mechanism for this chemical conversion involving loss of one carbon unit was described. This reaction scheme was suggested as a plausible chemical analogy for th

Full text of DOI:10.1016/S0040-4039(96)02276-9

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Article Doi

A plausible chemical analogy for biosynthesis of 2-arylbenzofuran of isoflavonoid origin and its application to synthesis of vignafuran

DOI: 10.1016/S0040-4039(96)02276-9

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(96)02276-9

Full text of DOI:10.1016/S0040-4039(96)02276-9

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