The synthesis of 1,6-disubstituted indanes which mimic the orientation of amino acid side-chains in a protein alpha-helix motif.
- 1 November 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (45) , 6879-6882
- https://doi.org/10.1016/s0040-4039(00)61800-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Solution structure of a calmodulin-target peptide complex by multidimensional NMRScience, 1992
- The structure of residues 7-16 of the A alpha-chain of human fibrinogen bound to bovine thrombin at 2.3-A resolution.Journal of Biological Chemistry, 1992
- Conformational constraints: Nonpeptide β‐turn mimicsJournal of Molecular Recognition, 1990
- (2S,5S,8S,11S)-1-Acetyl-1,4-diaza-3-keto-5-carboxy-10-thia-tricyclo -[2.8.04,8]-tridecane, 1 the preferred conformation of 1 (1 ≡ αTemp-OH) and its peptide conjugates αTemp-L-(Ala)n-OR (n=1 to 4) and α-Temp-L-Ala-L-Phe-L-Lys(εBoc)-L-Lys(ε-Boc)-NHMe studies of templates for α-helix formationTetrahedron Letters, 1988
- (2S,5S,8S,11S)-1-Acetyl-1,4-diaza-3-keto-5-carboxy-10-thia-tricyclo-[2.8.04,8]-tridecane, 1 synthesis of prolyl-proline-derived, peptide-functionalized templates for α-helix formationTetrahedron Letters, 1988
- 890. Friedel–Crafts acylation and alkylation. A comparison of inter- and intra-molecular processesJournal of the Chemical Society, 1956
- The structure of proteins: Two hydrogen-bonded helical configurations of the polypeptide chainProceedings of the National Academy of Sciences, 1951
- 770. Cyclisation of acid chlorides by Friedel–Crafts reactionsJournal of the Chemical Society, 1951