Cycloaddition of cyclobutenone and azomethine imine enabled by chiral isothiourea organic catalysts
The addition of an organic catalyst to the ketone moiety of a γ-mono-chloride substituted cyclobutenone destroys its stable, conjugated and nearly planar structure. The C–C bond in the resulting less stable anionic oxy-substituted non-planar intermediate is then activated. The breaking of one C–C si...
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| Main Authors: | , , , |
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| 格式: | Article |
| 語言: | English |
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2015
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| 在線閱讀: | https://hdl.handle.net/10356/96149 http://hdl.handle.net/10220/38479 |
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