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Pyranocyclopropanyl sugar amino acids, a new class of constrained (di)peptide isosteres

✍ Scribed by Martijn D.P. Risseeuw; Gijs A. van der Marel; Herman S. Overkleeft; Mark Overhand

Book ID
108284457
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
394 KB
Volume
20
Category
Article
ISSN
0957-4166

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πŸ“œ SIMILAR VOLUMES

A new approach to the stereoselective sy
A new approach to the stereoselective synthesis of conveniently protected Ξ±-allyl substituted amino acids; chiral key compounds in the synthesis of constrained peptide isostere constituents
✍ RamΓ³n Badorrey; Carlos Cativiela; Maria D. DΓ­az-de-Villegas; JosΓ©A. GΓ‘lvez; Yola πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 English βš– 448 KB

Enantiomerically pure ot-allyl-N-Boc-aminoamides were prepared by Curtius rearrangement of tx,ct-dialkyl chiral 2-cyanoesters obtained by the diastereoselective allylation of chiral 2-cyanoesters according to a modification of our previously described procedure.

ChemInform Abstract: A New Approach to t
ChemInform Abstract: A New Approach to the Stereoselective Synthesis of Conveniently Protected Ξ±-Allyl Substituted Amino Acids; Chiral Key Compounds in the Synthesis of Constrained Peptide Isostere Constituents.
✍ R. BADORREY; C. CATIVIELA; M. D. DIAZ-DE-VILLEGAS; J. A. GALVEZ; Y. LAPENA πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 32 KB πŸ‘ 2 views

rearrangement of the corresponding acylazides to the amine (VI). -(BADORREY, R.; CATIVIELA, C.;