A novel and convenient microwave-assisted dimerization of an active peptide compound using the DKPs as scaffold is described. The key reaction giving rise to the diketopiperazine scaffold is the intermolecular coupling. No epimerization was detected in the reactions used. Conventional and microwave heating of the reactions are compared. Synthesis by microwave irradiation gave the desired compounds in higher yields and in shorter reaction times than those obtained by conventional heating. © 2003 Elsevier Science Ltd. All rights reserved
Head-to-tail cyclization tetrapeptides can be improved using microwave dielec. heating. Cyclization...
4,5-Dicyanopyridazine (DCP) shows unexpected reactivity with dienophiles via Hetero Diels-Alder. Rea...
Multivalent dendrimeric peptides were synthesized via a microwave-assisted Huisgen 1,3-dipolar cyclo...
A novel and convenient microwave-assisted dimerization of an active peptide compound using the DKPs ...
Aqueous in situ one-pot N-Boc-deprotection-cyclization of Nα-Boc-dipeptidyl-tert-butyl and methyl es...
8siDipeptides and their cyclized 2,5-piperazinedione (or diketopiperazine, DKP) derivatives are attr...
Solution- and solid-phase Staudinger-mediated cyclizations were assessed to efficiently prepare hete...
The interest in the microwave assisted organic synthesis has been growing during the recent years. I...
The difficult coupling of \u3b1-aminoisobutyric acid (Aib), during the synthesis of dipeptides (), w...
The difficult coupling of a-aminoisobutyric acid (Aib), during the synthesis of dipeptides [Z-Aib-Va...
A modification of classical solid phase peptide synthesis methodol. under microwave irradn. was inve...
Abstract: A microwave-assisted, rapid solid phase peptide synthe-sis procedure is presented. It has ...
International audienceA solution phase synthesis of Peptide Nucleic Acid monomers and dimers was dev...
Aziridine derivatives involved in nucleophilic ring-opening reactions have attracted great interest,...
Aziridine derivatives involved in nucleophilic ring-opening reactions have attracted great interest,...
Head-to-tail cyclization tetrapeptides can be improved using microwave dielec. heating. Cyclization...
4,5-Dicyanopyridazine (DCP) shows unexpected reactivity with dienophiles via Hetero Diels-Alder. Rea...
Multivalent dendrimeric peptides were synthesized via a microwave-assisted Huisgen 1,3-dipolar cyclo...
A novel and convenient microwave-assisted dimerization of an active peptide compound using the DKPs ...
Aqueous in situ one-pot N-Boc-deprotection-cyclization of Nα-Boc-dipeptidyl-tert-butyl and methyl es...
8siDipeptides and their cyclized 2,5-piperazinedione (or diketopiperazine, DKP) derivatives are attr...
Solution- and solid-phase Staudinger-mediated cyclizations were assessed to efficiently prepare hete...
The interest in the microwave assisted organic synthesis has been growing during the recent years. I...
The difficult coupling of \u3b1-aminoisobutyric acid (Aib), during the synthesis of dipeptides (), w...
The difficult coupling of a-aminoisobutyric acid (Aib), during the synthesis of dipeptides [Z-Aib-Va...
A modification of classical solid phase peptide synthesis methodol. under microwave irradn. was inve...
Abstract: A microwave-assisted, rapid solid phase peptide synthe-sis procedure is presented. It has ...
International audienceA solution phase synthesis of Peptide Nucleic Acid monomers and dimers was dev...
Aziridine derivatives involved in nucleophilic ring-opening reactions have attracted great interest,...
Aziridine derivatives involved in nucleophilic ring-opening reactions have attracted great interest,...
Head-to-tail cyclization tetrapeptides can be improved using microwave dielec. heating. Cyclization...
4,5-Dicyanopyridazine (DCP) shows unexpected reactivity with dienophiles via Hetero Diels-Alder. Rea...
Multivalent dendrimeric peptides were synthesized via a microwave-assisted Huisgen 1,3-dipolar cyclo...