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Enol triflates coupling reactions

Enol triflates have emerged as attraetive alternatives to vinyl halides in the Stille coupling partner due to their ease of preparation from readily available carbonyl compounds. The addition of LiCI has been found to be beneficial to Stille enol triflate coupling reactions. Thus, it was not surprising that coupling 5-tributylstannylpyrimidine to enol triflate 134 proceeded in good yield in the presence of LiCI. In this case, the addition of Cul as cocatalysts was found to also be beneficial to the reaction outcome [57]. [Pg.491]

The coupling of the enol triflate 703 with the vinylstannane 704[397] has been applied to the synthesis of glycinoeclepin[576]. The introduction of a (Z)-propenyl group in the / -lactam derivative 705 proceeds by use of tri-2-furylphosphine[577]. However, later a smooth reaction to give the propenyl-iactam in 82% yield was achieved simply by treating with Pd(OAc)2 in NMP or CH2CI2 for 3-5 min without addition of LiCI and the phosphine ligand[578]. [Pg.232]

The intramolecular coupling of organostannanes is applied to macrolide synthesis. In the zearalenone synthesis, no cyclization was observed between arylstannane and alkenyl iodide. However, intramolecular coupling take.s place between the alkenylstannane and aryl iodide in 706. A similar cyclization is possible by the reaction of the alkenylstannane 707 with enol triflate[579]. The coupling was applied to the preparation of the bicyclic 1,3-diene system 708[580]. [Pg.233]

For examples of this coupling reaction involving enol triflates derived from ketones, see Takai, K. Taga-shira, M. Kuroda, T. Oshima, K. Utimoto, K. Nozaki, H. J. Am. Chem. Soc. 1986, 108, 6048. [Pg.786]

To avoid the retro-Diels-Alder reaction, 56 was dihydroxylated prior to the introduction of the bromine atom (57). Removal of the acetonide group followed by cleavage of the diol afforded a bis-hemiacetal. Selective reduction of the less-hindered hemiacetal group gave 58. The remaining hemiacetal was protected, and the ketone was converted to an enol triflate, thus concluding the synthesis of the electrophilic coupling component 51. [Pg.32]

Alkenyl trifluoromethanesulphonates (enol triflates) undergo Heck coupling with alkenes efficiently (equation 123)209a 215. This reaction is a useful variation of the use of vinyl halides not only because they are easy to prepare from the corresponding carbonyl compounds, but also because yields are good, and the stereochemistry of the triflate is largely maintained. [Pg.433]

The influence of catalytic C,C-coupling of six-membered cyclic nitronates can be used, under more drastic conditions, for the constmction of nitrogen-containing heterocycles via cascade chemical transformations (see, e.g., the coupling reaction of nitronate (368) with silyl enolates (369a-d) in the presence of trimethylsilyl triflate (154) (Scheme 3.211)). [Pg.639]

Tandem Sonogashira reactions starting with iodopyrrole 122 have furnished the dipyrrolylacetylene 124, and dimerization of 123 gives 125 [86], The Sonogashira coupling has also been reported for enol triflate 55 reacting with an /V-protected propargyl amine [81]. [Pg.53]

An application of Stille couplings to the solid phase using a traceless A-glycerol linker with 2-stannylindoles has been developed [177]. Only a few examples of the use of 3-stannylindoles in Stille reactions have been described. Ortar and co-workers prepared 169 and 170 and effected Pd-catalyzed cross coupling reactions with several aryl, heteroaryl, and vinyl substrates (bromides, iodides, triflates) to give the expected products 171 in high yields [178]. Enol triflates behave exceptionally well under the Ortar conditions, e.g., 172 to 173. [Pg.110]

The introduction of the allylic silane moiety required for the intermolec-ular Hosomi-Sakurai reaction is depicted in Scheme 16. Following the formation of the enol triflate 97, a Stille coupling provided excess to the allylic alcohol 98 [51]. The allylic alcohol (98) was endowed with a phosphate leaving group for the subsequent allylic substitution. Utilizing a trimethylsilyl cuprate as nucleophile for the 5 2 reaction, the allylic phosphate was converted into the allylic silane 89. A useful substrate-induced diastereoselectivity in favour of (14i )-89 was encountered at small scale but decreased significantly upon up-scaling. [Pg.96]

Clavepictines A and B were prepared using a variety of effective reactions on the piperidine ring, such as a silver-promoted cyclization of an aminoallene intermediate, diastereoselective alkylation, and cross coupling of an enol triflate <99JA10012>. [Pg.255]

Coupling with enol esters (7, 93). A new synthesis of an alkyl-substituted alkene involves coupling of a lithium dialkyl cuprate with an enol triflate,1 available from a ketone by reaction with triflic anhydride and 2,6-di-t-butylpyridine.2 A wide variety of organocuprates can be used and the geometry of the enolate is largely retained. Reported yields are in the range 60 100%. [Pg.282]

Although the coupling of aiyl halides with alkenes (commonly referred to as the Heck reaction) was first reported more than 25 years ago [ 1 ], only in the past decade has its enormous synthetic potential been realized [2], Within that time, the reaction has been extended to many substrates, including vinyl iodides and bromides and enol triflates. Moreover, the intramolecular variant has become one of the more important reactions for the formation of carbon-carbon bonds and has emerged as a premier method for the construction of quaternary carbon centers. The ability of intramolecular Heck reactions to reliably fashion carbon-carbon bonds in polyfunctional molecules has led to wide application of this reaction at the strategy level for the synthesis of complex natural products [2g],... [Pg.675]


See other pages where Enol triflates coupling reactions is mentioned: [Pg.256]    [Pg.218]    [Pg.227]    [Pg.230]    [Pg.231]    [Pg.183]    [Pg.593]    [Pg.597]    [Pg.715]    [Pg.776]    [Pg.185]    [Pg.1218]    [Pg.258]    [Pg.262]    [Pg.267]    [Pg.150]    [Pg.117]    [Pg.87]    [Pg.296]    [Pg.268]    [Pg.122]    [Pg.87]    [Pg.296]    [Pg.21]    [Pg.116]    [Pg.122]    [Pg.401]    [Pg.403]    [Pg.86]    [Pg.183]    [Pg.142]    [Pg.35]   


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