Trimethylenemethane. Trapping with butadiene, dimerization, and ring closure
P Dowd, G Sengupta, K Sachdev
Index: Dowd,P. et al. Journal of the American Chemical Society, 1970 , vol. 92, p. 5726 - 5727
Full Text: HTML
Citation Number: 19
Abstract
Vvi distinguished by nmr from those arising from cis-piperylene. Neither cis-nor trans- piperylene was isomerized in the course of the photolysis and there seem to be no common products between the two reactions. Moreover, that product which arises by attack on the more highly substituted doutle bond predominates in both cases. These two features, stereospecificity and attack on the more highly substituted double bond, clearly distinguish ...
Related Articles:
[Ramon, Diego J.; Yus, Miguel Tetrahedron Letters, 1992 , vol. 33, # 16 p. 2217 - 2220]
Trimethylenemethane, C (CH2) 3
[Doerr,R.G.; Skell,P.S. Journal of the American Chemical Society, 1967 , vol. 89, p. 3062 - 3064]
Synthesis and Structural Properties of Two Biscyclopropenes
[Golobish, Thomas D.; Dailey, William P. Journal of Organic Chemistry, 1995 , vol. 60, # 24 p. 7865 - 7869]
Synthesis and Structural Properties of Two Biscyclopropenes
[Golobish, Thomas D.; Dailey, William P. Journal of Organic Chemistry, 1995 , vol. 60, # 24 p. 7865 - 7869]
[Gomez, Cecilia; Ramon, Diego J.; Yus, Miguel Tetrahedron, 1993 , vol. 49, # 19 p. 4117 - 4126]