I would like to synthesize several N-term bromoacetamido peptides. I
wonder if I can use the standard solid phase way for that purpose, the
main question beeing the compatibility of that function with classical
cleavage-deprotection cocktail mixtures(obviously without EDT).
Thanks for any advice.
-- Jean LUCCHETTI, Ph.D. EUROGENTEC Bel S.A. Rue de l'Abbaye, 82-86 B-4040 HERSTAL (BELGIUM) Fax : (+ 32) 4 367 31 61 E-mail : <mailto:j.lucchetti@eurogentec.be> Web site : <http://www.eurogentec.be> <----check it out !