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- W2143849995 abstract "The simple refluxing of allenynes, having a phenylsulfonyl functionality on the allenyl group, in xylene (or mesitylene) without microwave irradiation resulted in the efficient formation of bicyclo[5.2.0]nona-1,7-dienes and bicyclo[4.2.0]octa-1,6-dienes in high yields. This method was shown to be successfully applicable to the first construction of bicyclo[6.2.0]deca-1,8-dienes. Construction of the corresponding oxa- and azabicyclo[m.2.0] frameworks could also be attained. This thermal ring-closing reaction involves the formal [2+2] cycloaddition in which the distal double bond of an allenyl moiety exclusively served as one of the pi-components regardless of the position of the phenysulfonyl functionality on the allenyl moiety." @default.
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- W2143849995 date "2007-05-18" @default.
- W2143849995 modified "2023-10-06" @default.
- W2143849995 title "Thermal [2+2] Cycloaddition of Allenynes: Easy Construction of Bicyclo[6.2.0]deca-1,8-dienes, Bicyclo[5.2.0]nona-1,7-dienes, and Bicyclo[4.2.0]octa-1,6-dienes" @default.
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- W2143849995 doi "https://doi.org/10.1021/jo070513p" @default.
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