Results 251 to 260 of about 120,164 (279)
Some of the next articles are maybe not open access.
Solid‐Phase Synthesis of DOTA–Peptides
Chemistry – A European Journal, 2004AbstractA general synthetic route to two DOTA‐linked N‐Fmoc amino acids (DOTA‐F and DOTA‐K) is described that allows insertion of DOTA at any endo‐position within a peptide sequence. Three model pentapeptides were prepared to test the general utility of these derivatives in solid‐phase peptide synthesis.
Luis M, De León-Rodriguez +3 more
openaire +2 more sources
Solid-Phase Synthesis of Lipidated Peptides
Journal of the American Chemical Society, 2002Characteristic partial structures of lipidated proteins embodying different lipid groups as well as additional fluorescent tags or a maleimide for coupling to proteins can be synthesized readily by means of a new solid-phase technique employing the oxidative cleavage of the hydrazide linker as well as on-resin farnesylation and palmitoylation after ...
Ludolph, B., Eisele, F., Waldmann, H.
openaire +3 more sources
Apparatus for Solid-Phase Peptide Synthesis
Science, 1967The apparatus, designed for solid-phase peptide synthesis, consists of a round-bottom flask, rocked on a wrist-shaker, and fitted with a special dropping funnel and a fritted filter disc embedded within the flask. The dropping funnel is designed to wash down the polymer adhering to the neck of the flask.
M C, Khosla, R R, Smeby, F M, Bumpus
openaire +2 more sources
Analytical Methods for Solid Phase Peptide Synthesis
Current Organic Chemistry, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
SABATINO, GIUSEPPINA +3 more
openaire +4 more sources
1991
This chapter discusses solid phase peptide synthesis, an idea which first appeared in a scientific publication by Merrifield in 1963. It explains why the term ‘solid phaseȉ is misleading, elaborating that the reactions do not take place in or on the surfaces of solid phases, but in gel systems produced by the penetration of solvent and solute molecules
openaire +1 more source
This chapter discusses solid phase peptide synthesis, an idea which first appeared in a scientific publication by Merrifield in 1963. It explains why the term ‘solid phaseȉ is misleading, elaborating that the reactions do not take place in or on the surfaces of solid phases, but in gel systems produced by the penetration of solvent and solute molecules
openaire +1 more source
Convergent solid‐phase peptide synthesis
International Journal of Peptide and Protein Research, 1991The solid‐phase synthesis, photolytic detachment from the solid support and purification in solution, of a fully‐protected octapeptide containing a methionine residue (protected as the sulphoxide) is described. Protection of methionine in this manner avoids problems associated with the oxidation of this residue during the photolysis.
PAUL LLOYD‐WILLIAMS +2 more
openaire +1 more source
1994
Abstract The chemical synthesis of oxytocin, with biological activity indistinguishable from that of the native hormone, by du Vigneaud and co-workers in 1953, represents a landmark in the application of synthetic peptides to the study of biology (1).
openaire +1 more source
Abstract The chemical synthesis of oxytocin, with biological activity indistinguishable from that of the native hormone, by du Vigneaud and co-workers in 1953, represents a landmark in the application of synthetic peptides to the study of biology (1).
openaire +1 more source
Active esters in solid-phase peptide synthesis
Journal of Protein Chemistry, 1989Incorporation of single amino acid residues into peptide chains built on insoluble polymeric supports a priori appeared promising: the use of isolated, well defined (and potentially commercially available) reactive intermediates were expected to reduce the extent of undesired side reactions.
M, Bodanszky, M A, Bednarek
openaire +2 more sources
1988
By the conventional methods of organic synthesis, preparation of peptides containing more than just a few amino acids is an arduous task. Introduction of blocking groups, coupling reactions and deprotection steps entail a large number of operations, such as washing the reaction mixtures neutral after coupling, precipitation or crystallization of ...
openaire +1 more source
By the conventional methods of organic synthesis, preparation of peptides containing more than just a few amino acids is an arduous task. Introduction of blocking groups, coupling reactions and deprotection steps entail a large number of operations, such as washing the reaction mixtures neutral after coupling, precipitation or crystallization of ...
openaire +1 more source

