Karthikeyan, Iyyanar ; Sekar, Govindasamy (2014) Iron-Catalyzed C-H Bond Functionalization for the Exclusive Synthesis of Pyrido[1,2-a]indoles or Triarylmethanols European Journal of Organic Chemistry, 2014 (36). pp. 8055-8063. ISSN 1434-193X
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Official URL: http://doi.org/10.1002/ejoc.201403233
Related URL: http://dx.doi.org/10.1002/ejoc.201403233
Abstract
An efficient iron-catalyzed C–H bond functionalization that proceeded through an intramolecular C–H amination reaction under nitrogen was employed for the synthesis of pyrido[1,2-a]indoles from 2-benzhydrylpyridines. Under oxygen, the same 2-benzhydrylpyridines were used for the synthesis of the corresponding tertiary alcohols. Overall, a change of atmosphere altered the course of the reaction.
Item Type: | Article |
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Source: | Copyright of this article belongs to John Wiley and Sons. |
ID Code: | 130981 |
Deposited On: | 02 Dec 2022 04:59 |
Last Modified: | 02 Dec 2022 04:59 |
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