Metal-free synthesis of 3,3-disubstituted oxoindoles by iodine(III)-catalyzed bromocarbocyclizations.
David C Fabry, Maciej Stodulski, Stefanie Hoerner, Tanja Gulder
文献索引:Chemistry 18(35) , 10834-8, (2012)
全文:HTML全文
摘要
"I" did it: An iodine(III)-mediated bromocarbocyclization was elaborated as an efficient tool for the synthesis of oxoindoles. This method is applicable to a variety of structurally different substrates, also with chemically sensitive groups, and gives access to the heterocycles in a regio- and stereoselective fashion. The indole-2-ones obtained can be converted easily into structurally complex target compounds, such as the alkaloid physostigmine.Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
相关化合物
相关文献:
2015-04-22
[J. Ethnopharmacol. 164 , 229-38, (2015)]
2015-10-27
[ACS Nano 9 , 9994-10004, (2015)]
2015-07-15
[ACS Appl. Mater. Interfaces 7 , 14905-11, (2015)]
2015-09-14
[Nanoscale 7 , 14413-21, (2015)]
2015-04-10
[Carbohydr. Res. 406 , 19-26, (2015)]