Nagireddy Attunuri, Naveen Kumar Muniganti, Babu Nanubolu Jagadeesh, Sridhar Reddy Maddi
Department of Organic Synthesis & Process Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500 007, India.
Academy of Scientific and Innovative Research, Ghaziabad, 201 002, India.
Chemistry. 2023 Dec 14;29(70):e202303245. doi: 10.1002/chem.202303245. Epub 2023 Oct 27.
Although challenging, the distant C-H functionalization with precision is quite rewarding and has long been intriguing. Tailoring an appropriate template accomplishes the job but the prerequisite sets the limitation. We herein unveil our discovery of annulation of alkynes on to two distant (from directing group) C-H bonds through rollover cyclometallation assisted by conjugated C=C bond. The annulation follows a concomitant cyclization rewarding a rare triple C-H functionalization. The annulation is totally regioselective with an array of unsymmetrical alkynes, taking the leverage of an extended conjugation or a tertiary hydroxyl co-ordination. The mechanism is supported by control experiments, KIE & labelling studies and Mass spectrometry.
尽管具有挑战性,但精确的远程C-H官能化非常有意义,并且长期以来一直引人入胜。定制合适的模板可以完成这项工作,但前提条件也设置了限制。我们在此揭示了通过共轭C = C键辅助的翻转环金属化,将炔烃环化到两个远程(与导向基团)C-H键上的发现。该环化反应伴随着环化,实现了罕见的三C-H官能化。利用扩展共轭或叔羟基配位,该环化反应对于一系列不对称炔烃具有完全的区域选择性。机理研究得到了对照实验、动力学同位素效应(KIE)和标记研究以及质谱分析的支持。