【摘 要】
:
A quinine-derived thiourea-catalyzed inter-/intramolecular Michael cycloaddition of chromone-oxindole/benzofuranone synthons with 3-substituted methylenebenzofu
【机 构】
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Guizhou Engineering Center for Innovative Traditional Chinese Medicine and Ethnic Medicine, Guizhou
论文部分内容阅读
A quinine-derived thiourea-catalyzed inter-/intramolecular Michael cycloaddition of chromone-oxindole/benzofuranone synthons with 3-substituted methylenebenzofuranones has been established, which constructed enantiomerically pure bispiro[benzofuran-oxindole/benzofuran-chromanone]s bearing five consecutive stereocenters including two spiro quatary carton centers in good yields (up to 93%) with high diastereoselectivities (up to>20:1 dr) and good enantioselectivities (up to>99%ee). Moreover, this is the first example of bifunctional chromone-benzofuranone synthon directed organocatalytic tandem reaction, and also the first example of the bispiro[benzofuran-oxindole] and bispirobenzofuranone, potentially useful in medicinal chemistry.
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