The Journal of Organic Chemistry
The acyl effect on intramolecular palladium-catalyzed trimethylenemethane cycloadditions
BM Trost, TA Grese
Index: Trost, Barry M.; Grese, Timothy A. Journal of Organic Chemistry, 1992 , vol. 57, # 2 p. 686 - 697
Full Text: HTML
Citation Number: 36
Abstract
Enhancing the generality of the intramolecular palladium-catalyzed [3+ 21 cycloaddition involving tri-methylenemethane complexes as reactive intermediates is possible by incorporation of acyl substituents on the TMM unit. Such substituted TMM-PdL2 species greatly expand the scope such that bicyclo [3.3. 0] octyl, bicyclo [4.3. 0] nonyl, and bicyclo [5.3. 0] decyl ring systems all can be created. Furthermore, the acyl-TMM chemistry ...
Related Articles:
[Rama Rao, A. V.; Deshmukh, M. N.; Sharma, G. V. M. Tetrahedron, 1987 , vol. 43, # 4 p. 779 - 784]