Efficient preparation of gamma-hydroxynitriles via nitrile enolate-epoxide reactions: Scope and diastereoselectivity. Taylor, S. K., DeYoung, D., Simons, L. J., Vyvyan, J. R., Wemple, M. A., & Wood, N. K. Synthetic Communications, 28(9):1691--1701, 1998. WOS:000073555900020
doi  abstract   bibtex   
The nucleophilic opening of epoxides by nitrile enolates using an efficient, convenient protocol is described The diastereoselectivity of this reaction was explored and found to give syn:anti ratios ranging from 1.1:1.0 to 4.8:1.0.
@article{ taylor_efficient_1998,
  title = {Efficient preparation of gamma-hydroxynitriles via nitrile enolate-epoxide reactions: Scope and diastereoselectivity},
  volume = {28},
  shorttitle = {Efficient preparation of gamma-hydroxynitriles via nitrile enolate-epoxide reactions},
  doi = {10.1080/00397919808006873},
  abstract = {The nucleophilic opening of epoxides by nitrile enolates using an efficient, convenient protocol is described The diastereoselectivity of this reaction was explored and found to give syn:anti ratios ranging from 1.1:1.0 to 4.8:1.0.},
  number = {9},
  journal = {Synthetic Communications},
  author = {Taylor, S. K. and DeYoung, D. and Simons, L. J. and Vyvyan, J. R. and Wemple, M. A. and Wood, N. K.},
  year = {1998},
  note = {{WOS}:000073555900020},
  pages = {1691--1701}
}

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