54125-08-5Relevant articles and documents
Evaluation of alkene isomerization as a trigger for enediyne activation
Semmelhack,Sarpong, Richmond,Bergman, Jeffrey,Ho, Douglas M.
, p. 541 - 544 (2007/10/03)
The concept of non-conjugated-to-conjugated double bond isomerization as a triggering mechanism for a calicheamicin model was tested. A bicyclo[7.3.1] enediyne framework was prepared with a bridgehead double bond and an acetonyl side chain. Base-promoted exchange failed to produce the conjugated isomer. Computational analysis suggested that additional conjugating groups would favor the isomerization, but experiment proved that not to be correct.
Preparation and Diels-Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes
Kozmin, Sergey A.,Rawal, Viresh H.
, p. 5252 - 5253 (2007/10/03)
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