Tag: Mikrowellensynthese Vorteile

Vor kurzem hat die American Peptide Society eine Reihe von E-Seminaren durchgeführt. Der Vortrag von Jon Collins über optimierte Synthese- und Reinigungsstrategien für Peptide gibt neue Perspektiven in der Peptid-Synthese sowie in der Aufreinigung.

Ein weiterer Höhepunkt der Vortrag zur schnellen Produktion von Neoantigenen, synthetischen Proteinen und das Scale-up der mikrowellengestützten Peptidsynthese auf Hunderte von mmol. Dieses Seminar beinhaltete auch Vorträge von Prof. Dr. Fernando Albericio und einen Vortrag vom Doktoranden Chih-Te „Ted“ Zee.

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#Peptidsynthese #Peptidaufreinigung #Prodigy #Liberty

Microwaves – „Yesterday“ Cover with Lyrics

So what does Microwave Digestion have to do with Paul McCartney? Most would say not much, but researchers at Abilene Christian University Department of Biochemistry have changed that.  Watch these researchers express the artistic side of chemistry as they cover The Beatles song „Yesterday“ with their own twist.


#Mikrowellensynthese #Mikrowelle

Mikrowellen-Synthese mit ganz viel Power im Discover 2.0
Ein häufiges Missverständnis ist, dass Mikrowellen-Synthesen ein polares Lösungsmittel benötigen. Polare Reagenzien/Edukte/Zwischenstufen interagieren im Discover 2.0 stark genug, um auch in unpolaren Lösungsmitteln effektiv zu erwärmen.

Unolare Lösemittel

Sehen Sie hier, wie eine mikrowellenbeschleunigte Diels-Alder-Reaktion in Toluol eine hervorragende Ausbeute liefert.

Umsetzung Diels Alder

Lesen Sie hier den kompletten Bericht: ApNote-Microwave-Chemistry-with-Non-polar-Reaction-Solutions-ap0186


23. Juni 2021
Die klassische chemische Synthese ist häufig sehr zeitaufwändig und bedarf einer anschließenden Aufreinigung bzw. Abtrennung der Nebenprodukte. Mittels Mikrowellen-Synthese erfolgen die Reaktionen bei hoher Ausbeute in wenigen Minuten. Die Handhabung von Reaktionen am Siedepunkt sowie Druckreaktionen ist dabei ganz einfach. Anschließend ermöglicht die Flash-Chromatographie eine schnelle und einfache Trennung der Produkte und Nebenprodukte.
Im Rahmen dieses Online-Seminars erläutern die Referenten Nina Meszaros (Axel Semrau) und Ulf Sengutta (CEM) die modernen Technologien.
In praktischen Übungen werden live die Geräte gezeigt. Und zudem können per Chat individuelle Fragen gestellt werden.
Um die Terminplanung zu erleichtern, bieten wir das Web-Seminar am Mittwoch, den 23. Juni 2021 zu zwei verschiedenen Uhrzeiten an: 10.00 Uhr und 14.00 Uhr (Dauer: ca. 1 Stunde)

Infos und Anmeldung

10. März 2021, ab 10.15 Uhr

Erleben Sie einen ganzen Tag interessante Vorträge zu den Neuigkeiten der Peptid-Synthese. Aufgrund der Corona-Situation können Präsenzvorträge derzeit nicht stattfinden. Deshalb veranstaltet CEM zusammen mit bekannten Forschern/innen dieses kostenfreie Online Seminar.

Academic Guest Speakers:

Professor Anna Maria Papini

University of Florence,

CY Cergy Paris Université

The challenge to design fully automated solid-phase MW-assisted cGMP ready processes of peptide production as active pharmaceutical ingredients 

Interdepartmental Research Unit of Peptide & Protein Chemistry and Biology, Departments  of Chemistry and NeuroFarBa, University of Florence (Italy)

With the increase of approved peptide-based drugs and patents expiring, the manufacturers’ need in production of peptides is dramatically rising. Companies involved in peptide-based drugs that have to be compliant with good manufacturing practices (GMP), face several challenges, such as high production costs on downstream processes (due to the use of high raw material amounts) and bad scalability. Therefore, the main challenge of production of active peptides as pharmaceutical ingredients is to find solutions to specific problems encountered during scale-up. 

As a proof-of concept we will report the strategies we investigated for the preparation of Eptifibatide, scalable to kilogram-scale, having in common the use of the microwave-assisted solid-phase peptide synthesis (MW-SPPS) procedure, which is now available not only at R&D level but also for the large-scale manufacturing of peptides. Following the very fast microwave-assisted Fmoc/tBu synthesis of the Eptifibatide linear precursor by a DIC/Oxyma Pure coupling protocol at 90 °C, we explored both the solution (off-resin) and the solid-phase (on-resin) disulfide bond formation.

The relevance of the strategy we optimized is essentially based on the selection of the StBu orthogonal protection on cysteine that is easily removed by MPA acting as a novel reducing agent for Cys(StBu) deprotection. Moreover, we demonstrated that all operations can be performed by fully automated process in the instrumentation.

To the best of our knowledge, this is a unique strategy performing all the processes including disulfide bond formation in a single reactor and represents an optimized scalable fully automated solid-phase microwave-assisted cGMP-ready process to prepare Eptifibatide.

Designing Synthetic Peptides to Explore the Dark Matter of Protein Space

Dek Woolfson

Schools of Chemistry and Biochemistry, & Bristol BioDesign Institute

University of Bristol, UK

Protein design—i.e., the construction of entirely new protein sequences that fold into prescribed structures—has come of age: it is now possible to generate a wide variety stable protein folds from scratch using rational and/or computational approaches.  A new challenge for the field is to move past protein structures offered up by nature and to target the so-called ‘dark matter of protein space’; that is, protein structures that should be possible in terms of chemistry and physics, but which biology seems to have overlook or not used prolifically.  This talk will illustrate what is currently possible in this nascent field using de novo a-helical coiled-coil peptides as building blocks for assembling larger, more-complex and functional protein-like structures.1

Coiled coils are bundles of 2 or more a helices that wrap around each other to form rope-like structures.  They are one of the dominant structures that direct natural protein-protein interactions. Our understanding of coiled coils provides a strong basis for building new proteins from first principles.  The first part of my talk will survey this understanding,1 our design methods,2,3 and our current “toolkit” of de novo coiled coils.4-5

Next, I will describe how the toolkit can be expanded used to generate some dark-matter protein structures.  I’ll focus on the rational and computational design of a-helical barrel proteins, which have 5 or more helices surrounding accessible central channels.6  Finally, I’ll discuss how these synthetic barrel proteins can be put to use to make new nanotube materials,7 rudimentary catalysts,8 membrane-spanning pores,9 and the components of a new types of sensing devices.10

Professor Dek Woolfson

University of Bristol

Professor Fernando Albericio

University of Barcelona,

University of Kwazulu-Natal

Microwave-Assisted Solid-Phase Peptide Synthesis, A Unique Tool for Peptide Research

Fernando Albericio,1,2 Beatriz G. de la Torre1

1University of KwaZulu-Natal, Durban 4001, South Africa; 2University of Barcelona, 08028-Barcelona, Spain

During the last five years (2016-2020), 18 drugs containing peptides have been approved by the US FDA.  In addition, several hundred are in clinical phases or advanced preclinical studies.   The development of new synthetic strategies has facilitated this explosion in the world of peptides. In this regard, the development of new resins, coupling reagents, protecting groups, and, more importantly, reliable and robust peptide synthesizers have been vital for the consolidation of the peptide drug market. 

In the field of automatic synthesizers, the last breakthrough occurred when at the beginning of this century, CEM launched the new concept of Microwave-Assisted SPPS. Our group and others have demonstrated that both couplings and Fmoc-removal are better performed in the microwave mode compared with classical synthesis or even with conventional heating. More important, this better performance in the two key reactions is not accompanied by any significant side-reaction. 

This presentation will discuss our last results on the use of Microwave synthesis for the preparation of intriguing peptides and/or for developing new synthetic strategies: (i) the preparation of staple peptides via late-stage C(sp2)-H Pd activation using the microwave; (ii) synthesis of N-alkyl amino acid containing peptides; (iii) development of new and more efficient coupling reagents; and (iv) microwave-based Green Solid-Phase Peptide Synthesis (GSPPS). 


In the GSPPS, the CEM Liberty Blue Microwave technology by itself could be considered green in terms of solvent consumption and time-saving and due to the excellent quality of the crude peptides, which enormously facilitates the purification with the consequent increase of yield and reduction of chromatography solvents.

Short antimicrobial peptides – discovery and optimization 

Kai Hilpert, St George’s University

The global health threat surrounding bacterial resistance has resulted in antibiotic researchers shifting their focus away from ‘traditional’ antibiotics and concentrating on other antimicrobial agents, including antimicrobial peptides.

These peptides exhibit broad-spectrum activity against bacteria, including multi-drug resistant strains, viruses, fungi, and protozoa, and constitute a major element of the innate immune system of many multicellular organisms.

We use the Spot-synthesis technique to study and optimize naturally occurring as well as artificial antimicrobial peptides. Understanding the features that make them antibacterial and hemolytic allows for targeted drug development. 

Associate Professor Kai Hilpert

St George’s University


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Peptid-Synthese im Liberty Blue

The insulin-like peptide human relaxin-2 was identified as a hormone that, among other biological functions, mediates the hemodynamic changes occurring during pregnancy. Recombinant relaxin-2 (serelaxin) has shown beneficial effects in acute heart failure, but its full therapeutic potential has been hampered by its short half-life and the need for intravenous administration limiting its use to intensive care units. In this study, we report the development of long-acting potent single-chain relaxin peptide mimetics. Modifications in the B-chain of relaxin, such as the introduction of specific mutations and the trimming of the sequence to an optimal size, resulted in potent, structurally simplified peptide agonists of the relaxin receptor Relaxin Family Peptide Receptor 1 (RXFP1) (e.g., 54). Introduction of suitable spacers and fatty acids led to the identification of single-chain lipidated peptide agonists of RXFP1, with sub-nanomolar activity, high subcutaneous bioavailability, extended half-lives, and in vivo efficacy (e.g., 64).

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A highly improved and green methodology for the direct amidation of carboxylic acids with amines using silica gel as a solid support and catalyst is described. The scope of this method is exemplified by the use of several aliphatic, aromatic, unsaturated and fatty acids. The reaction is also applied to different primary and secondary amines. Typically, the amines should be aliphatic, but aromatic amines can be used as well, though with lower yields. Several experiments to illustrate the selectivity of this methodology were also carried out with several more functionalized acids and amines. This approach is a substantial improvement over other previously described methods in amide synthesis.

Amine (1.5 mmol) and carboxylic acid (1.5 mmol) were dissolved in ethyl acetate (15 mL), then silica gel 60 230-400 mesh (1.0 g) was added. The solvent was removed under reduced pressure, the reactant mixture was transferred to a microwaves tube, and it was set to react in a CEM microwave reactor in cycles of 20 minutes at a power of 200 W maintaining constant temperature at 130 °C, and a hold time of 2 minutes. The reactant mixture was allowed to cool to room temperature, sonicated for 20 minutes with 30 mL of ethyl acetate, filtered, and the silica was washed with another 30 mL of ethyl acetate. The organic phase was washed with a saturated solution of NaHCO3 and HCl (10%), dried over MgSO4, filtered and the solvent was withdrawn under reduced pressure to obtain the pure product. In some cases flash chromatography was and it is indicated in the characterization data.

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Warum eigentlich Mikrowellen-Synthese?
Mikrowellenunterstützte Synthesen ermöglichen den Synthese-Chemikern ganz neue Wege zum gewünschten Produkt (Wirkstoff). Mit einem Höchstmaß an Flexibilität und bisher nicht vorhandenen Kontrollmöglichkeiten der Reaktionsparameter ermöglicht die Mikrowellen-Chemie ein direktes Einkoppeln der Energie in die gewünschten Reaktionen. In kürzester Zeit wird die notwendige Aktivierungsenergie der Reaktion zugeführt, was sich in der Beschleunigung gegenüber traditionellen Reaktionsbedingungen niederschlägt. So sind Zeitverkürzungen um den Faktor 100 bis 1000 keine Seltenheit. Die mikrowellenunterstützte Synthese ist zweifelsfrei der schnellste und der produktivste Weg zum gewünschten Wirkstoff. Über 5000 Literaturstellen mit stark zunehmender Tendenz berichten von den Möglichkeiten dieser Technologie

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This Feature Article gives an overview of microwave-assisted liquid phase routes to inorganic nanomaterials. Whereas microwave chemistry is a well-established technique in organic synthesis, its use in inorganic nanomaterials‘ synthesis is still at the beginning and far away from having reached its full potential. However, the rapidly growing number of publications in this field suggests that microwave chemistry will play an outstanding role in the broad field of Nanoscience and Nanotechnology. This article is not meant to give an exhaustive overview of all nanomaterials synthesized by the microwave technique, but to discuss the new opportunities that arise as a result of the unique features of microwave chemistry. Principles, advantages and limitations of microwave chemistry are introduced, its application in the synthesis of different classes of functional nanomaterials is discussed, and finally expected benefits for nanomaterials‘ synthesis are elaborated.

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