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Synthesis of Spiro Bis-Indanes via Domino Stetter-Aldol-Michael and Stetter-Aldol-Aldol Reactions: Scope and Limitations

机译:通过多米诺·斯特特-阿尔多-迈克尔和斯特特-阿尔多-阿尔多反应合成螺双-茚满:范围和局限性

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摘要

The synthesis of spiro bis-indanes by means of N-hetero-cyclic carbene (NHC) catalysis is reported. The dimerization of various o-formylchalcone substrates or their combination with phthaldialdehyde derivatives under the catalysis of thiazolium-derived carbenes afforded Stetter-aldol-Michael products and Stetter-aldol-aldol products, respectively. The use of poor Michael acceptors in conjunction with an N-alkyltriazolium-derived catalyst furnished a variety of dibenzo[8]annulene products. This work highlights the interplay of a variety of factors affecting competing pathways in NHC-catalyzed domino reactions.
机译:据报道,通过N-杂环卡宾(NHC)催化合成螺双茚满。在噻唑鎓衍生的卡宾催化下,各种邻甲酰基查耳酮底物的二聚化或它们与邻苯二甲醛衍生物的结合分别提供了Stetter-aldol-Michael产品和Stetter-aldol-aldol产品。将差的迈克尔受体与N-烷基三唑鎓衍生的催化剂结合使用可提供多种二苯并[8]环戊烯产品。这项工作强调了影响NHC催化的多米诺骨牌反应中竞争途径的多种因素之间的相互作用。

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