The regioselective aminohydroxylation of allylic carbamates

The synthesis and aminohydroxylation of a series of acyclic allylic carbamates is described: the formation of a putative O=Os=NR linkage between the transition metal and substrate is proposed to account for the high levels of regioselectivity that were observed; proof of the structure of one of the...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2001-10 (20), p.2078-2079
Hauptverfasser: Donohoe, T J, Johnson, P D, Helliwell, M, Keenan, M
Format: Artikel
Sprache:eng
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Zusammenfassung:The synthesis and aminohydroxylation of a series of acyclic allylic carbamates is described: the formation of a putative O=Os=NR linkage between the transition metal and substrate is proposed to account for the high levels of regioselectivity that were observed; proof of the structure of one of the aminohydroxylation products was obtained through X-ray crystallography.
ISSN:1359-7345
1364-548X
DOI:10.1039/b107253f