Stereoselective inverse conjugate addition of nitrogen and carbon nucleophiles to allenyl phosphine oxide. Synthesis of α,β-unsaturated phosphine oxides
Data(s) |
12/07/2013
12/07/2013
2012
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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 |
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 |