92278-77-8Relevant articles and documents
Direct Disulfide Formation from 2-Quinolinylmethyl Thioethers with Iron(III) or Copper(II) Salt
Yoshizawa, Hidenori,Otaka, Akira,Habashita, Hiromu,Fujii, Nobutaka
, p. 803 - 806 (1993)
2-Quinolinylmethyl thioethers were efficiently cleaved to generate the corresponding symmetrical disulfides using the following systems; FeCl3/N,N-dimethylformamide (DMF)/H2O, FeCl3/ethanol (EtOH)/H2O, and CuCl2/DMF/H2O.The 2-quinolinylmethyl group was utilized as a thiol protecting group in the synthesis of a model peptide.
Stereoselective synthesis of orthogonally protected α- methylnorlanthionine
Avenoza, Alberto,Busto, Jesus H.,Jimenez-Oses, Gonzalo,Peregrina, Jesus M.
, p. 2855 - 2858 (2007/10/03)
As the unusual amino acid norlanthionine (nor-Lan) has previously been incorporated into cyclic peptide analogues of the ring C of lantibiotic nisin, we report here the stereoselective synthesis of the new (S,R)- and (R,R)-α-methylnorlanthionines (α-Me-no