Microflow radical carboaminoxylations with a novel alkoxyamine

Inga C. Wienhöfer, Armido Studer*, Taifur Rahman, Takahide Fukuyama, Ilhyong Ryu

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

40 Scopus citations


Highly efficient thermal radical carboaminoxylations of various olefins by using the novel alkoxyamine A to give adducts of type B are described. It is reported that these radical addition reactions can be performed in a microflow reaction system. As compared to conventional batch reaction setup, significantly higher yields are obtained by running carboaminoxylations using the microflow system under analogous conditions.

Original languageEnglish
Pages (from-to)2457-2460
Number of pages4
JournalOrganic Letters
Issue number11
StatePublished - 4 Jun 2009

Fingerprint Dive into the research topics of 'Microflow radical carboaminoxylations with a novel alkoxyamine'. Together they form a unique fingerprint.

Cite this