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- W2100456449 endingPage "557" @default.
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- W2100456449 abstract "The monoamination of vicinal diols in the presence of in situ generated ruthenium catalysts has been investigated. Among the various phosphines tested in combination with [Ru(3)(CO)(12)], N-phenyl-2-(dicyclohexyl-phosphanyl)pyrrole showed the best performance. After optimization of the reaction conditions this system was applied to different secondary amines and anilines as well as a number of vicinal diols. With the exception of ethylene glycol, monoamination of the vicinal diols occurred selectively and the corresponding amino alcohols were obtained in good yields, producing water as the only side product." @default.
- W2100456449 created "2016-06-24" @default.
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- W2100456449 date "2009-06-17" @default.
- W2100456449 modified "2023-10-14" @default.
- W2100456449 title "Ruthenium‐catalyzed Selective Monoamination of Vicinal Diols" @default.
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- W2100456449 doi "https://doi.org/10.1002/cssc.200900034" @default.
- W2100456449 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19396884" @default.
- W2100456449 hasPublicationYear "2009" @default.