1993
DOI: 10.1002/chin.199340171
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ChemInform Abstract: Diels‐Alder Reaction of Fluorinated Benzoyl‐1,4‐benzoquinones and 1,5‐ Rearrangements of Their Adducts.

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“…Later, we carried out the Diels-Alder reaction of some fluorinated p-benzoquinones (221) with substituted dienes (222) furnishing the adducts 4a,5,8,8a-tetrahydro-1,4-naphthaquinones (223) in good yield (Scheme 66). 325 The potential utility of such a cycloaddition reaction lies in the synthesis of a number of anthracyclinone analogues. Similar Diels-Alder reactions of numerous 1,4-benzoquinones have been subsequently reported by our group.…”
mentioning
confidence: 99%
“…Later, we carried out the Diels-Alder reaction of some fluorinated p-benzoquinones (221) with substituted dienes (222) furnishing the adducts 4a,5,8,8a-tetrahydro-1,4-naphthaquinones (223) in good yield (Scheme 66). 325 The potential utility of such a cycloaddition reaction lies in the synthesis of a number of anthracyclinone analogues. Similar Diels-Alder reactions of numerous 1,4-benzoquinones have been subsequently reported by our group.…”
mentioning
confidence: 99%