Skip to content
2000
Volume 20, Issue 27
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

During the last decades, indium chemistry has attracted considerable attentions from synthetic community and has found widespread applications in organic synthesis. Compared to many other commonly used metals (such as Li, Al, Mg, and Zn), indium is insensitive to water and air, allowing the operation of indium-mediated organic transformations in aqueous media. In addition, its mildness also permits indium-mediated reactions to proceed with better functional group tolerance and sometimes better chemoselectivity. In this review, a wide variety of the applications of indium in organic synthesis are summarized, with a special emphasis on reactions which have been reported recently, such as allylation reaction, alkylation reaction, cross-dehydrogenative coupling (CDC), aldehyde and enone cross-coupling reaction, Prins-type cyclization, radical cyclization, propargylation/allenylation of imines, and Diels-Alder reaction.

Loading

Article metrics loading...

/content/journals/coc/10.2174/1385272820666160721155937
2016-12-01
2025-05-20
Loading full text...

Full text loading...

/content/journals/coc/10.2174/1385272820666160721155937
Loading

  • Article Type:
    Research Article
Keyword(s): aqueous media; Indium; organic synthesis; organoindium reagent
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test