877172-21-9Relevant academic research and scientific papers
Stereoselective palladium-catalyzed functionalization of homoallylic alcohols: A convenient synthesis of di- and trisubstituted isoxazolidines and β-amino-δ-hydroxy esters
Malkov, Andrei V.,Barlog, MacIej,Miller-Potucka, Lucie,Kabeshov, Mikhail A.,Farrugia, Louis J.,Kocovsky, Pavel
supporting information; experimental part, p. 6873 - 6884 (2012/07/17)
Enantiopure, Boc-protected alkoxyamines 12 and 13, derived from the readily available homoallylic alcohols 4 via a reaction that involves either inversion or retention of configuration, undergo a diastereoselective Pd-catalyzed ring-closing carbonylative
Influence of hydroxylamine conformation on stereocontrol in Pd-catalyzed isoxazolidine-forming reactions
Lernen, Georgia S.,Giampietro, Natalie C.,Hay, Michael B.,Wolfe, John P.
supporting information; experimental part, p. 2533 - 2540 (2009/08/07)
Palladium-catalyzed carboamination reactions between N-Boc-O-(but-3-enyl) hydroxylamine derivatives and aryl or alkenyl bromides afford cis-3,5- and trans-4,5-disubstituted isoxazolidines in good yield with up to >20:1 dr. The diastereoselectivity observe
Palladium(0)-catalyzed cascade one-pot synthesis of isoxazolidines
Dongol, Krishna Gopal,Tay, Boon Ying
, p. 927 - 930 (2007/10/03)
A highly diastereoselective cascade reaction protocol has been developed for the synthesis of isoxazolidine derivatives utilizing aryl halides, O-homoallyl hydroxylamine and palladium(0) in a one-pot reaction.
Palladium(II)-catalyzed synthesis of isoxazolidines: Using a catalytic copper acetate and molecular oxygen as the cooxidant
Dongol, Krishna Gopal,Boon, Ying Tay,Xiang, Kai,Thiemann, Thies
, p. 1247 - 1257 (2007/10/03)
An environmentally friendly process is reported for the palladium(II)-catalyzed cyclofunctionalization of allylic hydroxylamine derivatives using a catalytic amount of copper(II) acetate and molecular oxygen as the cooxidant. Copyright Taylor & Francis Gr
