By Henning Hopf, Michael S. Sherburn
ISBN-10: 3527334378
ISBN-13: 9783527334377
ISBN-10: 3527671188
ISBN-13: 9783527671182
ISBN-10: 3527671196
ISBN-13: 9783527671199
ISBN-10: 352767120X
ISBN-13: 9783527671205
ISBN-10: 3527671218
ISBN-13: 9783527671212
Filling a spot out there, this instruction manual presents a complete review of the attention-grabbing and increasing box of cross-conjugated molecules, their chemistry, synthesis and homes.
The editor is likely one of the world's prime scientists within the box, and has assembled the following a workforce of specialists to debate varied periods of molecules, in addition to using cross-conjugation for natural synthesis and functions in digital platforms and fabric technological know-how
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Halodendralenes are valuable substrates for dendralene to dendralene transformations that preserve or extend the dendralene framework. 26) [23], as are their nucleophilic relatives, pinacolatoboryldendralenes, in the synthesis of substituted [4]-, [5]-, and [6]dendralenes [25, 27]. (Pseudo)halodendralenes have also been used in Stille [209] and Sonagashira cross-couplings [178, 210]. Dendralene dimers can be obtained via homocoupling of halodendralenes [211]. Dendralene frameworks can also be extended by uncatalyzed metathesis reactions on alkynecontaining dendralenes, and olefination reactions on carbonyl-containing ones [1, 211–214], each of which has been discussed.
Cross conjugation : modern dendralene, radialene and fulvene chemistry by Henning Hopf, Michael S. Sherburn
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