An ethylene and terminal olefin equivalent in [4+ 2]. pi. cycloadditions. General synthetic application of phenyl vinyl sulfone to the construction of functionalized six- …
RVC Carr, LA Paquette
Index: Carr, Richard V. C.; Paquette, Leo A. Journal of the American Chemical Society, 1980 , vol. 102, # 2 p. 853 - 855
Full Text: HTML
Citation Number: 68
Abstract
The widespread use of the Diels-Alder reaction in synthetic organic methodology stems in large part from the frequent need to elaborate six-membered rings and the customarily high efficiency of such cycloadditions. A long-standing restriction to the universal application of this chemistry materializes when the diene and dienophile have no 7r-donor-acceptor complementarity. This phenomenon is witnessed perhaps most acutely in the case of ...
Related Articles:
[Carr, Richard V. C.; Williams, Richard V.; Paquette, Leo A. Journal of Organic Chemistry, 1983 , vol. 48, # 25 p. 4976 - 4986]
[Carr, Richard V. C.; Williams, Richard V.; Paquette, Leo A. Journal of Organic Chemistry, 1983 , vol. 48, # 25 p. 4976 - 4986]
[Carr, Richard V. C.; Williams, Richard V.; Paquette, Leo A. Journal of Organic Chemistry, 1983 , vol. 48, # 25 p. 4976 - 4986]