Author/Authors :
Davies، نويسنده , , David E. and Doyle، نويسنده , , Paul M. and Farrant، نويسنده , , R.Duncan and Hill، نويسنده , , Richard D. and Hitchcock، نويسنده , , Peter B. and Sanderson، نويسنده , , Paul N. and Young، نويسنده , , Douglas W.، نويسنده ,
Abstract :
The (3S,6S,10S)-7/5 bicyclic lactam 4, designed as an external turn constraint, was synthesised by a new stereoselective route involving Eschenmoser condensation. Calculated preferred conformations compare well with the preferred solid state conformation, obtained by X-ray crystallography. The lactam 4 was not a turn mimic in its own right but could be used as an external constraint to prepare the cyclic peptide 29 containing the integrin recognition motif GLDV. High-resolution NMR measurements were consistent with this compound having a single backbone conformation.
Keywords :
?-turn , bicyclic lactam , protein mimetic , Amino acid