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...
| Автори: | , , , |
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| Інші автори: | |
| Формат: | Journal Article |
| Мова: | English |
| Опубліковано: |
2015
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| Предмети: | |
| Онлайн доступ: | https://hdl.handle.net/10356/96149 http://hdl.handle.net/10220/38479 |