The bromination of olefins yielding a trans-1,2-dibromo-product was studied. Reagents were proposed to brominate the double bonds of cis-olefins mildly and stereospecifically. Reagents delivering two bromine atoms to the same side of olefins through a cyclic six-membered transition state were studied.
Carman,Derbyshire,Hansford,Kadirvelraj,Robinson
p. 117 - 126
(2007/10/03)
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