Dihydrobenzofurans via dienone-phenol rearrangement of spirooxetanes from photoaddition of quinones with electron donor olefins

DOI: 10.3987/com-95-7336

Source and publish data:

Heterocycles p. 619 - 624 (1996)

Update date:2022-08-04

Topics:

Authors:

Oshima, Takumi

Nakajima, Yu-Ichi

Nagai, Toshikazu

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Article abstract of DOI:10.3987/com-95-7336

Photoaddition of electron donor olefins such as vinyl ethers and stilbene to variously methyl- and halogeno-substituted 1,4-benzoquinones resulted in the formation of dihydrobenzofurans via a dienone-phenol rearrangement of the primary product spirooxetanes.

Full text of DOI:10.3987/com-95-7336

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