A microwave enhanced cross-metathesis approach to peptidomimetics
Functionalization of amino acid C- and N-termini with appropriate olefinic moieties allows for the generation of a peptidomimetic via a stereoselective cross-metathesis. This journal is The Royal Society of Chemistry.
Studies in the synthesis and reactivity of new chiral 1-[(trialkylsilyl)- methyl]propenamides
A very simple sequence of reactions such as cross-·metathesis using two catalysts and allylation to give the chiral hydroxyamide is described.
Bouzbouz, Samir
body text
p. 1888 - 1894
(2011/10/08)
Synthesis of small tripeptide molecules through a catalysis sequence comprising metathesis and aminohydroxylation
Tripeptidic structures were synthesized by using a combination of two independent consecutive catalytic procedures. Cross-metathesis of N-acroyl amino acid esters yields fumaric amide compounds with exclusive E double-bond geometry. This represents an unp
Streuff, Jan,Nieger, Martin,Muniz, Kilian
p. 4362 - 4371
(2008/02/07)
More Articles about upstream products of 56598-30-2