@inbook{735be1ca43b3483fb4cd5b4579852b06,
title = "Aminohydroxylation and Aminooxygenation of Alkenes",
abstract = "The aminohydroxylation of alkenes provides β-amino alcohols (vicinal amino alcohols). A number of alkene aminohydroxylation protocols (and those of related reactions termed oxyamination and aminooxygenation), predominantly enabled by transition-metal catalysis, are described in this chapter, which focuses on literature published in the period 1996-2015. Cyclic and acyclic compounds containing vicinal amino alcohols and derivatives thereof can be prepared from alkenes with good regio- diastereo- and enantioselectivity.",
keywords = "alkenes, aminohydroxylation, aminooxygenation, catalysis, copper catalysts, iron catalysts, manganese catalysts, osmium catalysts, oxyamination, palladium catalysts, rhodium catalysts, β-amino alcohols",
author = "Chemler, \{S. R.\} and T. Wdowik",
note = "Publisher Copyright: {\textcopyright} 2018. Thieme. All rights reserved.",
year = "2018",
doi = "10.1055/sos-SD-225-00172",
language = "English",
isbn = "9783132012318",
series = "Science of Synthesis",
publisher = "Georg Thieme Verlag",
number = "4",
pages = "343--388",
editor = "K. Mu{\c c}iz",
booktitle = "Science of Synthesis",
address = "Germany",
edition = "4",
}