322407-22-7Relevant academic research and scientific papers
Microwave-induced organometallic reactions in aqueous media. Use of Ga and Bi for the allylation of aromatic N-oxides and hydrazones
Laskar, Dhrubojyoti D.,Gohain, Mukut,Prajapati, Dipak,Sandhu, Jagir S.
, p. 193 - 195 (2002)
Homoallylic hydroxylamines and homoallylic hydrazides were synthesised in excellent yields by the reaction of allylgallium or allylbismuth reagent, generated in situ in the presence of 0.1 equivalent of NH4Cl-Bu4NBr, with aldonitrone
Indium mediated allylation of C=N compounds in aqueous media
Sampath Kumar,Anjaneyulu,Jagan Reddy,Yadav
, p. 9311 - 9314 (2000)
Allylindium adds to a variety of tosyl and aryl hydrazones derived from aromatic aldehydes and ketones at ambient temperature in a DMF-H2O solvent system to afford homoallylic tosyl hydrazides and homoallylic hydrazines, respectively. Homoallylic hydroxylamines were isolated via addition of allylindium to aldonitrones. (C) 2000 Elsevier Science Ltd.
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
Organometallic reaction in aqueous media. A samarium induced, efficient, synthesis of homoallyl hydroxylamines and hydrazides
Laskar, Dhrubojyoti D.,Prajapati, Dipak,Sandhu, Jagir S.
, p. 7883 - 7886 (2007/10/03)
Samarium can be used directly for the allylation of aldonitrones and hydrazones in aqueous media in the presence of Bu4NBr.
