Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1968, 33, 4008-4026
https://doi.org/10.1135/cccc19684008

Amino acids and peptides. LXXXVII. Optical rotatory dispersion of some β-aryl α-amino acids and model compounds

I. Frič, V. Špirko and K. Bláha

Crossref Cited-by Linking

  • Gálvez Nicanor, Moreno-Mañas Marcial, Vallribera Adelina, Molins Elies, Cabrero Araceli: Cobalt-mediated alkylation of (4R) and (4S)-3-acetoacetyl-4-benzyloxazolidin-2-ones. Preparation of enantiopure diphenylmethyl-, 9-fluorenyl- and (1-adamantyl)glycines. Tetrahedron Letters 1996, 37, 6197. <https://doi.org/10.1016/0040-4039(96)01322-6>
  • Meier Michael, Rüchardt Christoph: The Synthetic Potential of the Isocyanide‐Cyanide Rearrangement. Chem. Ber. 1987, 120, 1. <https://doi.org/10.1002/cber.19871200102>
  • Tiba Omar, Overberger C. G.: Synthesis, separation, and resolution of cis‐ and trans‐3‐ethylproline. J. Polym. Sci. A Polym. Chem. 1987, 25, 3437. <https://doi.org/10.1002/pola.1987.080251224>
  • Yang Wayne W.‐Y., Overberger C. G., Venkatachalam C. M.: Synthesis, characterization, and solution properties of 5‐ethyl‐substituted poly(L‐prolines). Synthesis of cis‐ and trans‐5‐ethyl‐L‐proline and optically active poly(cis‐5‐ethyl‐D‐proline). J. Polym. Sci. Polym. Chem. Ed. 1983, 21, 1643. <https://doi.org/10.1002/pol.1983.170210607>
  • Klyne W., Scopes P. M., Thomas R. N., Dahn H.: Optical Rotatory Dispersion and Circular Dichroism Part LXXV: Circular dichroism of some aryl‐amino acids [1]. Helvetica Chimica Acta 1971, 54, 2420. <https://doi.org/10.1002/hlca.19710540806>
  • Jorgensen Eugene C.: A sector rule for relating optical rotatory dispersion with the conformation and absolute configuration of α-amino acids. Tetrahedron Letters 1971, 12, 863. <https://doi.org/10.1016/S0040-4039(01)96575-X>