PHOTOLYSIS OF 4-SUBSTITUTED-4-HYDROXY-3-CYCLOBUTEN-1-ONES: A NEW ROUTE TO BUTENOLIDES FROM 4-HYDROXYCYCLOBUTENONES

DOI: 10.1016/0040-4039(88)85284-5

Source and publish data:

Tetrahedron Letters p. 3529 - 3532 (1988)

Update date:2022-08-04

Topics: Photolysis Experimental terms Route Butenolides

Authors:

Perri, Steven T.

Foland, Lafayette D.

Moore, Harold W.

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Article abstract of DOI:10.1016/0040-4039(88)85284-5

Photolysis of 4-substituted-4-hydroxy-3-cyclobuten-1-ones undergo electrocyclic ring opening followed by ring closure to provide butenolide products.This transformation is envisaged to involve a stereoselective disrotatory electrocyclic ring opening to co

Full text of DOI:10.1016/0040-4039(88)85284-5

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