872864-53-4Relevant academic research and scientific papers
The asymmetric aminohydroxylation route to GABOB and homoserine derivatives
Harding, Michael,Bodkin, Jennifer A.,Issa, Fatiah,Hutton, Craig A.,Willis, Anthony C.,McLeod, Malcolm D.
experimental part, p. 831 - 843 (2009/04/07)
The 4-nitrophenyl ether is an efficient directing group in the asymmetric aminohydroxylation reaction of homoallylic ether derivatives. Either regioisomeric product can be obtained with useful levels of enantioselectivity allowing for the short enantiosel
Substrate control in the asymmetric aminohydroxylation of monosubstituted alkenes: The enantioselective synthesis of GABOB and homoserine derivatives
Harding, Michael,Bodkin, Jennifer A.,Hutton, Craig A.,McLeod, Malcolm D.
, p. 2829 - 2831 (2007/10/03)
The 4-nitrophenyl ether is an efficient directing group in the asymmetric aminohydroxylation reaction of but-3-en-1-ol derivatives. Either regioisomeric product can be obtained with useful levels of enantioselectivity, allowing for the short enantioselect
