Organic & Biomolecular Chemistry · 2006 · 72 citations · 37 references
Natural SciencesChemistryMedicinal ChemistryGreen ChemistryOrganic ChemistryOrganometallic ChemistryOrganic SynthesisOrganometallic SynthesisRetrosynthetic AnalysisLate-stage Functionalization Via Cross-couplingMethylation PathwaysMild Reaction ConditionsOrganic Compound ReactionsPalladium CatalystsPet TracersTransition-metal-catalyzed Functionalization
The Pd(0)-mediated rapid coupling of methyl iodide with an excess of alkenyltributylstannane was examined with the aim of incorporating a short-lived 11C-labeled methyl group into a biologically significant organic compound with a 1-methylalkene unit for the synthesis of a PET tracer. Four sets of reaction conditions (A-D) were used, all performed in DMF at 60 degrees C for 5 min. Condition B, using CH3I/stannane/Pd2(dba)3/P(o-tolyl)3/CuCl/K2CO3 (1:40:0.5:4-6:2:5), works well in almost all cases. Condition D, using CH3I/stannane/Pd2(dba)3/P(o-tolyl)3/CuX (X = Br, Cl, or I)/CsF (1:40:0.5-5:2-20:2-20:5-50), shows the best results with regard to general applicability to tin substrates, affording the corresponding methylated product in >90% yield based on consumption of methyl iodide. P(t-Bu)2Me was less effective than P(o-tolyl)3, particularly for alpha,beta-unsaturated carbonyl substrates. No regio- or stereoisomerization occurred under these reaction conditions. The efficiency of the protocol was demonstrated by synthesis of an 11C-methylated compound.
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Ryōji Noyori · Angewandte Chemie International Edition · 2002 · 2K citations
Frédéric Paul, Joe Patt, John F. Hartwig · Journal of the American Chemical Society · 1994 · 835 citations