| Literature DB >> 21487614 |
Kentaro Okuma1, Nahoko Matsunaga, Noriyoshi Nagahora, Kosei Shioji, Yoshinobu Yokomori.
Abstract
An efficient route to a variety of 2-phenylindolin-3-ones from amino acid methyl esters has been developed. The reaction of amino acid methyl esters with benzyne prepared from 2-(trimethylsilyl)phenyl triflate and CsF gave 2-phenylindolin-3-ones in moderate to good yields. © The Royal Society of Chemistry 2011Entities:
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Year: 2011 PMID： 21487614 DOI： 10.1039/c1cc11234a
Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222