4.7 Article

Total synthesis of (±)-alantrypinone by hetero Diels-Alder reaction

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 69, Issue 1, Pages 79-85

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo030273n

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An efficient total synthesis of (+/-)-alantrypinone 4 by hetero Diels-Alder reaction of a novel pyrazine diene 9 with either a functionalized 3-alkylideneoxindole or 3-methyleneoxindole itself is described. The Diels-Alder reactions provide both the desired regiochemistry and exo selectivity. An interesting anionic equilibration between alantrypinone 4 and its epimer 31 or between its ester analogues 23 and 24 has been demonstrated, and a mechanism has been proposed.

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