【摘 要】
:
A variety of indoloazocines can be readily prepared by 8-endo-dig cyclization of alkynylindole substrates and following rearrangement by catalysis of Ph3PAuNTf2 or other gold complexes.The reaction co
【机 构】
:
State Key Laboratory of Coordination Chemistry,Nanjing National Laboratory of Microstructures,School
【出 处】
:
The 24th International Society of Heterocyclic Chemistry Con
论文部分内容阅读
A variety of indoloazocines can be readily prepared by 8-endo-dig cyclization of alkynylindole substrates and following rearrangement by catalysis of Ph3PAuNTf2 or other gold complexes.The reaction conditions are exceptionally mild, and a range of functional groups are easily tolerated.
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