炔烃
炔基化
组合化学
化学
催化作用
范围(计算机科学)
脱羧
可扩展性
羧酸
反应条件
有机化学
计算机科学
程序设计语言
数据库
作者
Joel M. Smith,Tian Qin,Rohan R. Merchant,Jacob T. Edwards,Lara R. Malins,Zhiqing Liu,Guanda Che,Zichao Shen,Scott A. Shaw,Martin D. Eastgate,Phil S. Baran
标识
DOI:10.1002/anie.201705107
摘要
Abstract The development of a new decarboxylative cross‐coupling method that affords terminal and substituted alkynes from various carboxylic acids is described using both nickel‐ and iron‐based catalysts. The use of N‐hydroxytetrachlorophthalimide (TCNHPI) esters is crucial to the success of the transformation, and the reaction is amenable to in situ carboxylic acid activation. Additionally, an inexpensive, commercially available alkyne source is employed in this formal homologation process that serves as a surrogate for other well‐established alkyne syntheses. The reaction is operationally simple and broad in scope while providing succinct and scalable avenues to previously reported synthetic intermediates.
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