The preparation of α-tetralones from benzocyclobutenones via sequential thermal electrocyclic reactions
DN Hickman, TW Wallace, JM Wardleworth
Index: Hickman, Derek N.; Wallace, Timothy W.; Wardleworth, J. Michael Tetrahedron Letters, 1991 , vol. 32, # 6 p. 819 - 822
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Citation Number: 19
Abstract
Abstract 1-Alkenylbenzocyclobuten-1-ols, prepared from benzocyclobutenones via the addition of alkenylmagnesium bromides, or the addition of alkynyllithium reagents followed by (E)-selective reduction of the triple bond, undergo successive thermal 4π and 6π electrocyclic reactions leading to substituted 3, 4-dihydro-1 (2H)-naphthalenones.
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