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- W2003404780 abstract "The synthesis, NMR structure determination, and molecular modelling of the conformationally restricted diastereomeric sugar azido acids 1 and 2 are presented. The bicyclic structures of these compounds are obtained through a iodocyclization reaction on the C-allyl glycoside of the D-arabinofuranose. Cyclic tetrapeptide 11 containing the amino acid derived from 1 linked to the RGD sequence has been synthesized; this compound was found to be a selective antagonist of αvβ3 integrins expressed on GM 7373 cells." @default.
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- W2003404780 date "2002-02-07" @default.
- W2003404780 modified "2023-09-27" @default.
- W2003404780 title "Arabinose-derived bicyclic amino acids: synthesis, conformational analysis and construction of an αvβ3-selective RGD peptide" @default.
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- W2003404780 doi "https://doi.org/10.1039/b110453e" @default.
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