Alkynylation cuprates

Aldehydes and ketones have also been prepared by nucleophilic cleavage of resin-bound O-alkyl hydroxamic acids (Weinreb amides [744]) with lithium aluminum hydride [745] or Grignard reagents (Entries 1 and 2, Table 3.41). Similarly, support-bound thiol esters can be cleaved with Grignard reagents to yield ketones [272], or with reducing agents to yield aldehydes (Entry 3, Table 3.41). Polystyrene-bound sele-nol esters (RCO-Se-Pol) react with alkynyl cuprates to yield alkynyl ketones [746]. 

Bicyclic enediynes were obtained from the Diels-Alder adducts of cyclopenta-diene or furan with bis phenyliodonium acetylene triflate and lithium alkynyl cuprates. In this case the reaction conditions were more demanding and yields less satisfactory. 

This type of copper-catalysed reaction was also extended to the alkynylation of alkenyldiiodonium salts (48), through reaction with lithium alkynyl cuprates. 

Stang, P. J., Blume, T. and Zhdankin, V. V. 1993. Synthesis of enediynes by reaction of bicy-cloalkenyldiiodonium salts with lithium alkynyl cuprates. Synthesis 1 35-36. 

Addition of an alkynyl cuprate to a cationic tricarbonyl(ri -dienyl)iron precursor is a key step in the synthesis of an iron containing HETE analog (Scheme 4-194). ... 

Dieter developed a flexible two step synthesis of substituted pyrroles involving initial Beak deprotonation of /ert-butoxycarbonyl (Boc) amines 36 followed by addition of CuX-2LiCl (X = -Cl, -CN) to afford a-aminoalkylcuprates. Such cuprates undergo conjugate addition reactions to a,(3-alkynyl ketones affording a,(3-enones 37, which upon treatment with PhOH/TMSCl undergo carbamate deprotection and intramolecular cyclization to afford the pyrroles 38 . 

An alternative route to allenyl stannanes involves organocuprate displacements on propargylic chlorides bearing an alkynyl PhsSn substituent (equation 39)79. Interestingly, transmetallation by attack of the cuprate on the tin substituent is not observed in these systems. A parallel strategy can be employed for allenylgermanes (equation 39)79. The... 

A cuprate prepared in situ from tBuPh2SiLi and Cul has been found to react with alkynyl epoxides to afford allenylsilanes (Eq. 9.43) [50]. Enantioenriched alkynyl epoxides, which are readily prepared in high yield through Sharpless asymmetric epoxidation [51], afford chiral allenylsilanes with anti stereoselectivity. 

A large variety of cuprates are known nowadays. They include heteroleptic derivatives R(Y)CuM (Y = alkynyl, halide, amido, alkoxide, thiolato, phosphide M = Li or Mg), and have found widespread application in organic chemistry. Their syntheses and applications are discussed in the other chapters of this book. In addition, compounds in which the copper to lithium (or magnesium) ratio differs from 1 1 are also known examples are R3CuLi2 and the so-called higher order cyanocuprates introduced by Lipshutz et al. [99]. 

A smoother transmetalation procedure should be ensured by the more electronegative character of aluminium, as first demonstrated by Wipf and Ireland [35]. Thus, hydroalumination of 1-hexyne with DIBAL-H, followed by addition of the cuprate 59, bearing non-transferable alkynyl groups, provides the copper intermediate 60. This adds smoothly to 2-cyclohexenone to produce the Michael adduct 61, in 72% yield (Scheme 2.18) [36],... 

The recognition of the importance of cluster structure has resulted in a new understanding of the role of a dummy ligand (Y) in the chemistry of mixed cuprates MeCu(Y)Li [145]. As shown in Scheme 10.15 for the case of Y =alkynyl, the... 

As indicated in Section ni.B, deprotonation of a carbamate affords a dipole-stabilized a-amino-organolithium that can be transmetalated with copper salts to form cuprates, thereby expanding the versatility of the organolithium. Suitable electrophiles include enones, alkenyl, alkynyl, allenyl and dienyl carboxylic acid derivatives, nitriles and sulfoxides. Dieter and coworkers have shown that the same process can be accomplished via transmetalation of a stannane (Scheme 36). The procedure is particularly... 

Secondary and tertiary dialkylcuprates, lithium dialkenyl-, and even diphenyl-cuprates, add in very good yields to the reactive propionaldehyde diethyl acetal. The syn addition products may be trapped with a variety of electrophiles such as alkyl, alkenyl, alkynyl and aryl halides. The method has been used for the synthesis of several natural products. Substituted alkynic acetals also react with lithium dialkylcuprates in ether to furnish stable dialkenylcuprates of type (128) which do not eliminate to the corresponding alkoxy allenes (129) if the temperature is maintained below -20 C.164-179... 

---