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Organocopper complexes organometallics

The most important substrates for substitutions of this type are alkenyl and aryl triflates, bromides, or iodides (Sections 16.1-16.4). The most important organometallic compounds to be introduced into the substrates contain Cu, Mg, B, Zn or Sn. The metal-bound C atom can be sp2-, sp2-, or. sp-hybridized in these compounds, and each of these species, in principle, is capable of reacting with unsaturated substrates. Organocopper compounds often (Section 16.1, 16.2), but not always substitute without the need for a catalyst (Section 16.4.5). Grignard compounds substitute in the presence of catalytic amounts of Ni complexes (Section 16.3), while organoboron (Section 16.4.2), organozinc (Section 16.4.3) and organotin (Section 16.4.4) compounds are typically reacted in the presence of Pd complexes (usually Pd(PPhj)4). [Pg.691]

Formation of metal-carbon bonds by addition of an organometallic reagent to an unsaturated compound or a diazonium compound is a little-used method in organocopper chemistry. Various alkylcopper reagents, (RCu + MgXg or LiX), add to acetylene or the alkynes, RC=CH, in a cis manner in ether or ether-pentane at low temperatures (223). A 7T-complex is a probable intermediate. The vinylcopper addition product obtained is dependent on the nature of the alkyne, being sensitive to electronic effects in the latter ... [Pg.229]

Discussed in this chapter, for the most part, are documented cases where complexes derived fiom (one or more equivalents of) a Grignard or organolithium reagent, in combination with a copper(I) salt, have been used to add to an aldehyde, ketone, imine, amide or nitrile moiety. In the majority of examples, the key issue is one of stereocontrol. Hence, where available, data within the organocopper manifold versus those for other organometallic reagents are provided for comparison. [Pg.107]

Activation of the G=N moiety by the addition of BF3 0Et2 has increased the scope of organometallic additions (Table 2). Akiba and coworkers have shown that lithium alkynides treated with BF3 OEt2 add to substituted aldimines (entry 1, Table BF3 complexes of organocopper and di-... [Pg.361]


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See also in sourсe #XX -- [ Pg.217 , Pg.218 , Pg.219 , Pg.220 , Pg.221 , Pg.222 ]




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Organocopper

Organocoppers

Organometallics organometallic complexes

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