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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Bibliographic Details
Main Authors: Li, Bao-Sheng, Wang, Yuhuang, Jin, Zhichao, Chi, Robin Yonggui
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2015
Subjects:
Online Access:https://hdl.handle.net/10356/96149
http://hdl.handle.net/10220/38479
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Institution: Nanyang Technological University
Language: English