Condensation Reactions To Form Oxazoline-Substituted Potassium Organotrifluoroborates
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چکیده
منابع مشابه
A novel route to organonitrites by Pd-catalyzed cross-coupling of sodium nitrite and potassium organotrifluoroborates.
Microwave irradiated palladium-catalyzed cross-coupling reaction of potassium styryltrifluoroborates and sodium nitrite gives the corresponding styryl nitrites in high yields. Potassium aryltrifluoroborates also furnish aryl nitrites under same reaction condition. This unprecedented cross-coupling is an interesting development and has the potential to lead to new nitration protocols.
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Reaction of (S)-2-ferrocenyl-4-(1-methylethyl)oxazoline with [Cp*IrCl2]2 in benzonitrile with KPF6 and NaOH gave (η(5)-(S)-2-(4-(1-methylethyl))oxazolinylcyclopentadienyl)(η(5)-pentamethylcyclopentadienyl)iridium(iii) hexafluorophosphate (68%). This transformation of an iron-based into an iridium-based metallocene proceeds via the rearrangement, with loss of cyclopentadienyliron, of an intermed...
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A general method for the alkenylation of alkyl electrophiles using nearly stoichiometric amounts of the air- and moisture-stable potassium organotrifluoroborates has been developed. Various functional groups were tolerated on both the nucleophilic and electrophilic partner. Reactions of highly substituted E- and Z-alkenyltrifluoroborates, as well as vinyl- and propenyltrifluoroborates, were suc...
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ژورنال
عنوان ژورنال: Organic Letters
سال: 2009
ISSN: 1523-7060,1523-7052
DOI: 10.1021/ol901395c