Selective nucleophilic transformations of cyclopentadienone epoxides

DOI: 10.1016/S0040-4020(01)82039-1

Source and publish data:

Tetrahedron p. 2593 - 2610 (1990)

Update date:2022-08-04

Topics:

Authors:

Houwen-Claassen, Adrie A. M.

Klunder Klunder

Zwanenburg

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Article abstract of DOI:10.1016/S0040-4020(01)82039-1

Acid-catalysed solvolyses of cyclopentadienone epoxides lead to epoxide ring opening and take place regioselectively at C-4. The stereochemical outcome of the epoxide ring opening depends on the substitution pattern and the nature of the substituents. Tra

Full text of DOI:10.1016/S0040-4020(01)82039-1

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