615264-92-1Relevant academic research and scientific papers
Straightforward synthesis of depsiphosphonopeptides via Mannich-type multicomponent condensation
Xu, Jiaxi,Gao, Yuanhe
, p. 783 - 788 (2007/10/03)
A straightforward method for the synthesis of depsiphosphonopeptides via a Mannich-type multicomponent condensation of simple starting materials, such as benzyl carbamate, aldehydes, and 1-carbethoxyalkyl phosphorodichloridites, was developed. Compared to
Thiourea-Catalyzed Enantioselective Hydrophosphonylation of Imines: Practical Access to Enantiomerically Enriched α-Amino Phosphonic Acids
Joly, Guy D.,Jacobsen, Eric N.
, p. 4102 - 4103 (2007/10/03)
Chiral thiourea 1b catalyzes the highly enantioselective hydrophosphonylation of a wide range of N-benzyl imines. The hydrophosphonylation products are readily deprotected by hydrogenolysis, providing access to free α-amino phosphonic acids in highly enantioenriched form. Copyright
High-performance liquid chromatographic enantiomer separation and determination of absolute configurations of phosphinic acid analogues of dipeptides and their α-aminophosphinic acid precursors
Laemmerhofer, Michael,Hebenstreit, Dieter,Gavioli, Elena,Lindner, Wolfgang,Mucha, Artur,Kafarski, Pawel,Wieczorek, Piotr
, p. 2557 - 2565 (2007/10/03)
The enantiomers of N-benzyloxycarbonyl-phosphinic pseudodipeptides and their N-benzyloxycarbonyl-α-aminophosphinic acid precursors as well as various other structural analogues were separated on a set of cinchona alkaloid-derived chiral anion-exchangers b
