期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 74, 期 16, 页码 6390-6393出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo9011859
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The efficient Suzuki cross-coupling of pyrazoline nonaflates with organoboron reagents was achieved to afford diverse 3-substituted-2-pyrazolines in excellent yield. The nonaflates displayed improved reactivity over the corresponding triflates and smoothly coupled to a variety of aryl- and heteroarylboronic acids. This process and its broad scope constitute a rapid, divergent strategy for the synthesis of elaborated 2-pyrazolines that are not readily obtained via conventional methods.
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