Bicyclo nonadiene complexes

The metal-mediated and metal-catalyzed [6 + 2]- and [6 + 4]-cycloaddition reactions, pioneered by Pettit and co-workers105 106 and Kreiter and co-workers,107 respectively, involve the cycloaddition of metal-complexed cyclic trienes with 7r-systems such as alkenes, alkynes, and dienes. The [6 + 2]-reactions produce bicyclo[4.2.1]nonadiene derivatives and the [6 + 4]-reactions produce bicyclo[4.4.1]undecatrienes (Scheme 32). Trienes complexed to chromium, which can be prepared on large scale (40 g) as reported by Rigby and co-workers,108 react with 7r-systems upon thermolysis or irradiation.109-111 Chromium and iron-catalyzed [6 + 2]-reactions of cycloheptatrienes and disubstituted alkynes... 

In the nickel(II) and cobalt(II)complexes of phosphabicyclo[3.3.1]nonanes 282 (246) and 283 (247), respectively, the bicyclo systems exist in a CC conformation according to X-ray data. Some complex compounds incorporating the bicyclo[3.3.1]nonadienes as ligands have been studied for example, X-ray data were reported for the platinum(II) complex 284 (248). 

The [4+3] cycloaddition reaction offers a convenient way to prepare relatively complex seven-membered rings from simple starting materials. Using MBH adducts 352 as C3 component, a phosphine-catalyzed [4 + 3] annulation has been developed to construct the bicyclo[3.2.2]nonadiene skeleton (Scheme 4.112). The reactions proceeds smoothly with various MBH adducts as well as various substituted pyrones 353 such as ester, nitrile and amide substituted pyrones, resulting in compounds 354 in moderate to good yields. 

Mukai et al. have found scission of a cyclopentane ring of allenyne 34 in the rhodium-catalyzed cycloisomerization (Scheme 7.11) [14]. When 34 was treated with a rhodium catalyst, the bicyclo [7.4.0]tridecatriene 37 was formed. Mechanistically, initial coordination of 34 to rhodium(I) would occur between an allenic distal double bond and an alkyne to form the intermediary ir-coordinating complex, which undergoes oxidative cyclization to form the rhodabicyclo[4.3.0]nonadiene intermediate 35. Subsequent P-carbon elimination, presumably assisted by release of the ring strain of the cyclopentane (6.3 kcal mol ), results in the formation of the 10-membered rhodacycle 36. Reductive elimination ensues to give the final product 37. 

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