| Literature DB >> 11784201 |
Abstract
Trialkylphosphines furnish unusual, sometimes unique, reactivity in a range of transformations. Unfortunately, their utility is compromised by their sensitivity to oxidation. We have examined a simple but powerful strategy for addressing this problem: convert air-sensitive trialkylphosphines into air-stable phosphonium salts via protonation on phosphorus. These robust salts serve as direct replacements for the corresponding phosphines (simple deprotonation under the reaction conditions by a Brønsted base liberates the trialkylphosphine) in a diverse set of applications. [reaction: see text]Entities:
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Year: 2001 PMID: 11784201 DOI: 10.1021/ol016971g
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005