Unknown

Dataset Information

0

Silicon-initiated carbonylative carbotricyclization and [2+2+2+1] cycloaddition of enediynes catalyzed by rhodium complexes.


ABSTRACT: The reaction of dodec-11-ene-1,6-diynes or their heteroatom congeners with a hydrosilane catalyzed by Rh(acac)(CO)2 at ambient temperature and pressure of CO gives the corresponding fused 5-7-5 tricyclic products, 5-oxo-1,3a,4,5,7,9-hexahydro-3H-cyclopenta[e]azulenes or their heteroatom congeners, in excellent yields through a unique silicon-initiated cascade carbonylative carbotricyclization (CO-SiCaT) process. It has also been found that the 5-7-5 fused tricyclic products can be obtained from the same type of enediynes and CO through a novel intramolecular [2+2+2+1] cycloaddition process. The characteristics of these two tricyclization processes and the fundamental differences in their reaction mechanisms are discussed. This novel higher-order cycloaddition reaction has also been successfully applied to the tricyclization of undeca-5,10-diyn-1-als, affording the corresponding 5-7-5 fused-ring products bearing a seven-membered lactone moiety. Related [2+2+2] tricyclizations of enediyne and diynal substrates are also discussed. These newly discovered reactions can construct multiple bonds all at once, converting linear starting materials to polycyclic compounds in a single step. Thus, these new processes provide innovative routes to functionalized polycyclic compounds that are useful for the syntheses of natural and unnatural products.

SUBMITTER: Bennacer B 

PROVIDER: S-EPMC2538960 | biostudies-literature | 2005 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Silicon-initiated carbonylative carbotricyclization and [2+2+2+1] cycloaddition of enediynes catalyzed by rhodium complexes.

Bennacer Bibia B   Fujiwara Masaki M   Lee Seung-Yub SY   Ojima Iwao I  

Journal of the American Chemical Society 20051201 50


The reaction of dodec-11-ene-1,6-diynes or their heteroatom congeners with a hydrosilane catalyzed by Rh(acac)(CO)2 at ambient temperature and pressure of CO gives the corresponding fused 5-7-5 tricyclic products, 5-oxo-1,3a,4,5,7,9-hexahydro-3H-cyclopenta[e]azulenes or their heteroatom congeners, in excellent yields through a unique silicon-initiated cascade carbonylative carbotricyclization (CO-SiCaT) process. It has also been found that the 5-7-5 fused tricyclic products can be obtained from  ...[more]

Similar Datasets

| S-EPMC5975726 | biostudies-literature
| S-EPMC5966446 | biostudies-literature
| S-EPMC3646433 | biostudies-literature
| S-EPMC3069138 | biostudies-literature
| S-EPMC4508204 | biostudies-literature
| S-EPMC5833981 | biostudies-literature
| S-EPMC3480994 | biostudies-literature
| S-EPMC5073370 | biostudies-literature
| S-EPMC2929375 | biostudies-literature
| S-EPMC2917183 | biostudies-literature