Asymmetric transition-metal-catalyzed allylic alkylations: applications in total synthesis.

@article{Trost2003AsymmetricTA,
  title={Asymmetric transition-metal-catalyzed allylic alkylations: applications in total synthesis.},
  author={Barry M Trost and Matthew Lantz Crawley},
  journal={Chemical reviews},
  year={2003},
  volume={103 8},
  pages={
          2921-44
        }
}
A. Primary Alcohols as Nucleophiles 2931 B. Carboxylates as Nucleophiles 2931 C. Alkylations with Phenols 2932 IV. Nitrogen Nucleophiles in AAA Total Synthesis 2935 A. Alkylamines as Nucleophiles 2935 B. Azides as a Nucleophile 2936 C. Sulfonamide Nucleophiles 2937 D. Imide Nucleophiles 2938 E. Heterocyclic Amine Nucleophiles 2940 V. Sulfur Nucleophiles 2941 VI. Summary and Conclusions 2941 VII. Acknowledgment 2941 VIII. References 2942 I. Considerations for Enantioselective Allylic Alkylation 
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Unpublished results. CR020027W Asymmetric Transition-Metal-Catalyzed Allylic Alkylations

  • B. W. Metcalf, P. Tetrahedron Lett. Casara
  • J. Am. Chem. Soc
  • 1975
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Unpublished results . ( 7 ) For a recent review , see :

  • B. M. Trost, M. L. Crawley, F. D. Toste

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