Aminomethylations via Cross-Coupling of Potassium Organotrifluoroborates with Aryl Bromides
摘要:
[GRAPHICS]The Suzuki-Miyaura cross-coupling reaction of N,N-dialkylaminomethyltrifluoroborates with aryl halides allows the construction of an aminomethyl aryl linkage through a disconnection based on dissonant reactivity patterns. A variety of these aminomethyltrifluoroborate substrates were prepared in good to excellent yields and then shown to cross-couple with equal facility to both electron-rich and electron-poor aryl halides as well as to a variety of heteroaromatic bromides.
Aminomethylations via Cross-Coupling of Potassium Organotrifluoroborates with Aryl Bromides
作者:Gary A. Molander、Deidre L. Sandrock
DOI:10.1021/ol070543e
日期:2007.4.1
[GRAPHICS]The Suzuki-Miyaura cross-coupling reaction of N,N-dialkylaminomethyltrifluoroborates with aryl halides allows the construction of an aminomethyl aryl linkage through a disconnection based on dissonant reactivity patterns. A variety of these aminomethyltrifluoroborate substrates were prepared in good to excellent yields and then shown to cross-couple with equal facility to both electron-rich and electron-poor aryl halides as well as to a variety of heteroaromatic bromides.