N-H insertion reactions of rhodium carbenoids. Part 2. Preparation of N-substituted amino(phosphoryl)acetates (N-substituted phosphorylglycine esters).


Autoria(s): Ferris, L.; Haigh, David; Moody, C.J.
Data(s)

1996

Resumo

Rhodium(II) acetate-catalyzed reaction of Et 2-diazo-2-diethoxyphosphorylate, EtO2CC(:N2)PO(OEt)2, with carbamates, amides, ureas or anilines gives a range of N-substituted 2-amino-2-diethoxyphosphorylacetates, EtO2CCH(NHR1)PO(OEt)2 (where R1 = Boc, Cbz, acetyl, propionyl, pivaloyl, n-Pr, Ph and substituted Ph groups), by N-H insertion reaction of the intermediate rhodium carbenoid.

Identificador

http://pure.qub.ac.uk/portal/en/publications/nh-insertion-reactions-of-rhodium-carbenoids-part-2-preparation-of-nsubstituted-aminophosphorylacetates-nsubstituted-phosphorylglycine-esters(21b77de3-1e13-44ba-a424-479673a93fcc).html

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Ferris , L , Haigh , D & Moody , C J 1996 , ' N-H insertion reactions of rhodium carbenoids. Part 2. Preparation of N-substituted amino(phosphoryl)acetates (N-substituted phosphorylglycine esters). ' Journal of the Chemical Society - Perkin Transactions 1 , vol - , pp. 2885-2888 .

Tipo

article