Stereoselective inverse conjugate addition of nitrogen and carbon nucleophiles to allenyl phosphine oxide. Synthesis of α,β-unsaturated phosphine oxides


Autoria(s): Santos Ruiz, Jesús Manuel de los; Ochoa Díez, Zelai; Palacios Gambra, Francisco Javier
Data(s)

12/07/2013

12/07/2013

2012

Resumo

Issue in Honor of Prof. Paweł Kafarski

[EN] The reactivity of new three carbon synthon, generated in situ from the reaction of electrondeficient allenes with an appropriate phosphine as the catalyst, toward pronucleophilic reagents is described. Triphenylphosphine-catalyzed reaction of allenes derived from phosphine oxides with nitrogen- or carbonucleophiles gave the γ-addition product as a mixture of cis and trans isomers.

Identificador

ARKIVOC 4: 54-62 (2012)

1551-7012

http://hdl.handle.net/10810/10413

Idioma(s)

eng

Publicador

ARKAT USA, Inc

Relação

http://quod.lib.umich.edu/cgi/p/pod/dod-idx/stereoselective-inverse-conjugate-addition-of-nitrogen.pdf?c=ark;idno=5550190.0013.406

Direitos

© ARKAT-USA, Inc. This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 License.

info:eu-repo/semantics/openAccess

Palavras-Chave #allenyl phosphine oxide #phosphine catalysis #pronucleophiles #umpolung addition #α,β-unsaturated phosphine oxides
Tipo

info:eu-repo/semantics/article