A radical cyclisation reaction based strategy to 2,3,5-tri- and tetrasubstituted furans

DOI: 10.1016/S0040-4020(01)90088-2

Source and publish data:

Tetrahedron p. 7901 - 7910 (1990)

Update date:2022-08-05

Topics:

Authors:

Srikrishna

Sundarababu

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Article abstract of DOI:10.1016/S0040-4020(01)90088-2

Synthesis of 2,3,5-trisubstituted furans (5), starting from 2-methoxypropene and 1,3-disubstituted propargyl alcohols 3, via the radical cyclisation of the bromo acetal 4 followed by aromatisation, is reported. Analogously, 1-methoxycyclohexene and propar

Full text of DOI:10.1016/S0040-4020(01)90088-2

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