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   <subfield code="a">A study of the Claisen rearrangement of 7-(3-phenyl-2-propenyloxy)-3-phenyl-(4 H )-1-benzopyran-4-one derivatives</subfield>
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   <subfield code="a">Die Claisen-Umlagerung von 7-(3-Phenyl-2-propenyloxy)-3-phenyl-(4 H )-1-benzopyran-4-on</subfield>
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   <subfield code="a">Summary: The Claisen rearrangement of 7-(3-phenyl-2-propenyloxy)-3-phenyl-(4H)-1-benzopyran-4-one (2 a) gave 7-hydroxy-8-(1-phenyl-2-propenyl)-3-phenyl-(4H)-1-benzopyran-4-one (3 a) and 2,3-dihydro-2,6-diphenyl-3-methyl-(7H)furo[2,3-h]-1-benzopyran-7-one (7 a). 2-Methyl-7-(3-phenyl-2-propenyloxy)-3-phenyl-(4H)-1-benzopyran-4-one (2 b) afforded4 b and7 b. 8-Methyl-7-(3-phenyl-2-propenyloxy)-3-phenyl-(4H)-1-benzopyran-4-one (12) gave only the alkali soluble product 7-hydroxy-8-methyl-6-(1-phenyl-2-propenyl)-3-phenyl-(4H)-1-benzopyran-4-one (13).3 a,4 b, and13 were further cyclized in acidic medium to9 a,10 b, and14 followed by dehydrogenation.</subfield>
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