Tetrahedron Letters p. 7831 - 7834 (1992)
Update date:2022-09-26
Topics:
Pasto, Daniel J.
Alonso, David E.
The elimination of nitrogen from the 1,1-diazine 11 produces the homotrimethylenemethane diradical 12 which undergoes ring closure to form the substituted methylenencyclobutanes 13 and 14.No cleavage of the diradical intermediate to produce 1,1-dimethylallene and styrene is observed. Key Words: Homotrimethylenemethane; Diradical Intermediate; Methylenecyclobutane; Allene <2+2> Cycloaddition; Diradical Ring-Closure
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Doi:10.1021/jm00072a007
(1993)Doi:10.1021/ja01634a039
(1954)Doi:10.1007/s10593-020-02673-w
(2020)Doi:10.1002/jhet.5570320203
(1995)Doi:10.1021/ja00199a055
(1989)Doi:10.1016/j.ica.2010.02.020
(2010)
