Regioselective Synthesis of Highly Substituted Naphthols

DOI: 10.1021/jo00108a029

Source and publish data:

Journal of Organic Chemistry p. 644 - 649 (1995)

Update date:2022-08-05

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Authors:

Turnbull, Philip

Moore, Harold W.

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Article abstract of DOI:10.1021/jo00108a029

2,3,4-Trisubstituted 4-hydroxy-2-cyclobuteones, prepared by regiospecific synthesis of substituted cyclobutenediones, undergo Lewis acid facilitated ionization to cyclobutenyl cations, which are trapped by trialkylsilanes in a regioselective sense.Thermol

Full text of DOI:10.1021/jo00108a029

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Product name:2-(1-hexynyl)-4-hydroxy-3-isopropoxy-4-phenyl-2-cyclobutenone

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