82933-21-9Relevant articles and documents
Demonstration of Exclusive α-Peptidation at the Micellar Interface
Ranganathan, Darshan,Ranganathan, Subramania,Singh, Girij Pal,Patel, Bhisma Kumar
, p. 525 - 528 (2007/10/02)
Microreactors, dispersed in iso-octane, harboring water pools and crafted from AOT and co-surfactant condensing agent DODCI, exclusively direct α-peptidation, thus reversing the normal preference of glutamic acid and aspartic acid for side chain carboxyl group amidation.
L-METHIONINE OXIDATION: NOVEL AND UNANTICIPATED TRANSFORMATIONS WITH 4-tBUTYL IODOXYBENZENE
Ranganathan, S.,Ranganathan, D.,Singh, S.K.,Bhattacharyya, D.,Shanthy, S.,Singh, G.P.
, p. 5363 - 5366 (2007/10/02)
4-tButyl iodoxybenzene transforms Bz-Met-OMe to products arising from, S oxidation and C-H insertion followed by degradation.Z-Met(sulfoxide)-OMe is very effective in bringing about ester hydrolysis via intramolecular attack.The S oxidation to sulfoxides and then to sulfones can be monitored and controlled, proceeds with chiral retention, affects neither the peptide bond nor the protecting groups and has been further illustrated with,Z-Gly-Met-OMe, Z-Met-OMe and Z-S(benzyl)-Cys-OMe.