Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis

  • Kazmaier U
ISSN: 0008-4166
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Abstract

Palladium-catalyzed allylic substitution is one of the main reactions for testing new chiral ligands. The most relevant examples from the work published in the period 2007 to mid-2010 are reviewed. The vast majority of the work published within this timeframe relies upon the application of chiral ligands for asymmetric induction. The recent advances in the development and applications of new chiral P-P, P-N, P-O, P-S, N-N, N-S, S-S, and NHC ligands are covered and are the main focus of this chapter. Other aspects of enantioselective palladium allylic alkylations are discussed in the subsequent sections, for example, heterogeneous catalysis, the use of chiral salt additives, and recent applications in kinetic resolution. © 2011 Springer-Verlag Berlin Heidelberg.

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Kazmaier, U. (2012). Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. (U. Kazmaier, Ed.), Vol. 3 Springer, New York (Vol. 38, p. 179). Springer Berlin Heidelberg. Retrieved from http://link.springer.com/10.1007/978-3-642-22749-3 http://www.springer.com/gb/book/9783642227486%5Cnhttp://link.springer.com/10.1007/978-3-642-22749-3

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