FeCl3 Catalyzed
Regioselective C‑Alkylation of Indolylnitroalkenes
with Amino Group
Substituted Arenes
Posted on 2014-02-21 - 00:00
An efficient FeCl3 catalyzed protocol for the synthesis
of amino functionalized indolylnitroalkanes from easily
available precursor indolylnitroalkenes and substituted amines
has been developed. Regioselective C-alkylation in
the presence of free amino substituted arenes occurred. The scope
of this methodology shows good functional group tolerance, and further,
this protocol was used to prepare indolylquinoline derivatives.
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Zanwar, Manoj
R.; Kavala, Veerababurao; Gawande, Sachin D.; Kuo, Chun-Wei; Huang, Wen-Chang; Kuo, Ting-Shen; et al. (2016). FeCl3 Catalyzed
Regioselective C‑Alkylation of Indolylnitroalkenes
with Amino Group
Substituted Arenes. ACS Publications. Collection. https://doi.org/10.1021/jo4025368
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AUTHORS (9)
- MZManoj R. ZanwarVKVeerababurao KavalaSGSachin D. GawandeCKChun-Wei KuoWHWen-Chang HuangTKTing-Shen KuoHHHsiu-Ni HuangCHChiu-Hui HeCYChing-Fa Yao
