111865-48-6Relevant articles and documents
α,β-Unsaturated imines via Ru-catalyzed coupling of allylic alcohols and amines
Rigoli, Jared W.,Moyer, Sara A.,Pearce, Simon D.,Schomaker, Jennifer M.
supporting information; experimental part, p. 1746 - 1749 (2012/04/23)
A convenient synthesis of α,β-unsaturated imines requiring only an allylic alcohol, an amine and a Ru catalyst has been developed. The use of large excesses of oxidant and the purification of sensitive intermediates can be avoided.
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
Synthesis of β,γ-Unsaturated Amino Acids by the Strecker Reaction
Greenlee, W. J.
, p. 2632 - 2634 (2007/10/02)
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