Chelating phosphines with C2 and C3 symmetry

Amide formation between ring opened aziridines and 2-(diphenylphosphino)benzoic acid provides an easy access to chelating di- and triphosphines with C 2 and C 3 symmetry.

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Bibliographic Details
Published inMendeleev communications Vol. 14; no. 6; pp. 276 - 277
Main Authors Brulé, Emilie, Pei, Yuxin, Lake, Fredrik, Rahm, Fredrik, Moberg, Christina
Format Journal Article
LanguageEnglish
Published 2004
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Summary:Amide formation between ring opened aziridines and 2-(diphenylphosphino)benzoic acid provides an easy access to chelating di- and triphosphines with C 2 and C 3 symmetry.
ISSN:0959-9436
1364-557X
DOI:10.1070/MC2004v014n06ABEH002026