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Synthesis 2020; 52(02): 239-245
DOI: 10.1055/s-0039-1690220
DOI: 10.1055/s-0039-1690220
paper
Silver-Promoted Regioselective Oxidative Decarboxylative C–H Alkylation of Phenanthridines with Carboxylic Acids
Autor*innen
We thank the National Natural Science Foundation of China (No. 21672136, 21871174, 21772215) and Innovation Program of Shanghai Municipal Education Commission (No. 2019-01-07-00-09-E00008) for financial support.
Weitere Informationen
Publikationsverlauf
Received: 12. September 2019
Accepted after revision: 02. Oktober 2019
Publikationsdatum:
29. Oktober 2019 (online)

§ These authors contributed equally to this manuscript
Abstract
A novel oxidative decarboxylative C–H alkylation of phenanthridines with carboxylic acids was developed for the efficient synthesis of multi-substituted phenanthridine derivatives. The given method features easy availability of starting materials, high regioselectivity, and mild conditions. Furthermore, a one-pot synthesis of multi-substituted phenanthridine derivatives was realized by the reaction of biphenyl isocyanides and carboxylic acid.
Key words
phenanthridine - decarboxylation - silver acetate - C–H alkylation - potassium persulfate - late-stage modificationSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0039-1690220.
- Supporting Information (PDF) (opens in new window)
-
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