Dibromoketones reactions with enamines

The reaction of a,a -dibromoketones with enamines in the presence of some activating agents gives [3 + 2] cycloadducts. The reagents that have been used so far are... 

Fe2(CO)g and CeClj—SnClj the latter present some advantages like lower toxicity, lower temperature and homogeneous reaction conditions. The first step in the reaction ofa,a -dibromoketone 56 with CeClj—SnClj (equation 10) involves a single debromina-tion in analogy with a Reformatsky reaction to afford a cerium a-bromo enolate 57, This intermediate suffers from further elimination of bromide via ionization to oxyallyl cation 58 which undergoes the [3 + 2] cycloaddition to the enamine. The aminocyclo-pentanonc 59 obtained was easily deaminated to cyclopentenone 60. 

Reaction of a,a -dibromoketones with enneacarbonyldiiron gives oxoallyl cations which easily react with alkenes, enamines, and amides via [3+2] and with dienes via [3+4] cycloadditions, respectively, in high yield (Scheme 10.8) [26-29],... 

Another synthetically useful carbon bond-forming reaction involves reaction of diiron nonacarbonyl with halo-carbonyl compounds. Noyori found that a,a -dibromoketones (498) react with diiron nonacarbonyl [Fe2(CO)9] to give an iron stabilized alkoxy zwitterion (499). The intermediate Jt-allyl iron species reacts with alkenes in a stepwise manner (initially producing 500) to give cyclic ketones such as 501, 23 and the product is equivalent to the product of a [3-t2]-cycloaddition with an alkene (sec. 11.11). This cyclization method is now known as Noyori annulation. This reaction is related to the Nazarov cyclization previously discussed in Section 12.3.C. Enamines can react with 498, but the initially formed enamino ketone product eliminates the amino group to form cyclopentanone derivatives. Intermediates such as 499 may actually exist as cations hound to a metal rather than as the alkoxide-iron structures shown.323b-d noted that Zn/B(OEt)3 is... 

Other Reactions Oxallyls, formed from a,a -dibromoketones and Fe2(CO)9, react with alkenes, enamines, enol ethers, amides, or dienes to give a variety of [3 + 2] and [3 + 4] cycloaddition products (Eq. 14.71). This provides a very short synthesis of the tropane skeleton from acetone and pyrrole (Eq. 14.72). As shown in Eq. 14.71, an oxallyl resembles trimeth-ylenemethane (5.22) except that one =CH2 of 5.22 is replaced by =0. 

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