Design and synthesis of a conformationally restricted trans peptide isostere based on the bioactive conformations of saquinavir and nelfinavir.


Journal article


Michael K. Edmonds, Andrew D. Abell
Journal of Organic Chemistry, vol. 66(11), 2001 Apr 3, pp. 3747-3752

Cite

Cite

APA   Click to copy
Edmonds, M. K., & Abell, A. D. (2001). Design and synthesis of a conformationally restricted trans peptide isostere based on the bioactive conformations of saquinavir and nelfinavir. Journal of Organic Chemistry, 66(11), 3747–3752.


Chicago/Turabian   Click to copy
Edmonds, Michael K., and Andrew D. Abell. “Design and Synthesis of a Conformationally Restricted Trans Peptide Isostere Based on the Bioactive Conformations of Saquinavir and Nelfinavir.” Journal of Organic Chemistry 66, no. 11 (April 3, 2001): 3747–3752.


MLA   Click to copy
Edmonds, Michael K., and Andrew D. Abell. “Design and Synthesis of a Conformationally Restricted Trans Peptide Isostere Based on the Bioactive Conformations of Saquinavir and Nelfinavir.” Journal of Organic Chemistry, vol. 66, no. 11, Apr. 2001, pp. 3747–52.


BibTeX   Click to copy

@article{michael2001a,
  title = {Design and synthesis of a conformationally restricted trans peptide isostere based on the bioactive conformations of saquinavir and nelfinavir.},
  year = {2001},
  month = apr,
  day = {3},
  issue = {11},
  journal = {Journal of Organic Chemistry},
  pages = {3747-3752},
  volume = {66},
  author = {Edmonds, Michael K. and Abell, Andrew D.},
  month_numeric = {4}
}


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