143900-34-9Relevant academic research and scientific papers
Enantiomerically divergent pathways in Tsuji-Trost reactions: exploiting the structural differences between β-acyloxy-o-(diphenylphosphino)benzamides and β-amido-o-(diphenylphosphino)benzoates
Nelson, Brandon M.,Chavda, Mihir K.,Oliphant, Jonathan,King, Jalisa M.,Szczepura, Lisa F.,Hitchcock, Shawn R.
, p. 1075 - 1080 (2016)
Using a single chiral scaffold, (1R,2S)-norephedrine, a series of monophosphine ligands have been prepared. The ligands prepared, β-acyloxy-(o-diphenylphosphino)amides and β-amido-(o-diphenylphosphino)esters, give rise to enantiomerically divergent produc
Synthesis of N4-substituted[1,3,4]oxadiazinan-2-ones derived from norephedrine
Casper, David M.,Nora, George P.,Blackburn, Jennifer R.,Bentley, Jeromy T.,Taylor, Deanna C.,Hitchcock, Shawn R.
, p. 823 - 828 (2007/10/03)
[1,3,4]-Oxadiazinan-2-ones bearing substitution at the N4-position have been synthesized from norephedrine in good yield via N-alkylation, nitrosation, reduction and cyclization.
N-ALKYLOXAZABOROLIDINES DERIVED FROM EPHEDRINES
Tlahuext, Hugo,Contreras, Rosalinda
, p. 727 - 730 (2007/10/02)
The synthesis of oxazaborolidines from amides derived from ephedrine and pseudoephedrine by treatment with BH3-THF is reported.The reaction affords chiral oxazaborolidines with nitrogen atom substituents of different steric requirements enlarging the pote
