Waldemar Iwanek

Prof. Waldemar Iwanek

UTP, University of Science and Technology, Faculty of Chemical Technology and Engineering, Seminaryjna 3, 85-326 Bydgoszcz
orcid

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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KMKrystian Miazek
Krystian Miazek
WIWaldemar Iwanek
Waldemar Iwanek
CRClaire Remacle
Claire Remacle
ARAurore Richel
Aurore Richel
DGDorothée Goffin
Dorothée Goffin
Microalgae are a source of numerous compounds that can be used in many branches of industry. Synthesis of such compounds in microalgal cells can be amplified under stress conditions. Exposure to various metals can be one of methods applied to induce cell stress and synthesis of target products in microalgae cultures. In this review, the potential of producing diverse biocompounds (pigments, lipids, exopolymers, peptides, phytohormones, arsenoorganics, nanoparticles) from microalgae cultures upon exposure to various metals, is evaluated. Additionally, different methods to alter microalgae response towards metals and metal stress are described. Finally, possibilities to sustain high growth rates and productivity of microalgal cultures in the presence of metals are discussed.

1 August 1995 in European Journal of Organic Chemistry
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WIWaldemar Iwanek
Waldemar Iwanek
JMJochen Mattay
Jochen Mattay

1 November 2005 in Journal of Chromatography A
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Journal Article
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ARAlexander Ruderisch
Alexander Ruderisch
WIWaldemar Iwanek
Waldemar Iwanek
JPJens Pfeiffer
Jens Pfeiffer
GFGert Fischer
Gert Fischer
KAKlaus Albert
Klaus Albert
VSVolker Schurig
Volker Schurig

31 July 1992 in Journal of Photochemistry and Photobiology A: Chemistry
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Journal Article
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WIWaldemar Iwanek
Waldemar Iwanek
JMJochen Mattay
Jochen Mattay

1 November 2009 in Mini-Reviews in Organic Chemistry
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WIWaldemar Iwanek
Waldemar Iwanek
AWAlicja Wzorek
Alicja Wzorek
Resorcinarenes constitute a very attractive class of macrocycles possessing a cavity capable of complexing small molecules. They can be simply transformed into chiral derivatives by functionalisation of their hydroxy groups as well as the “ortho” position at the resorcinol ring. The appropriate modifications lead to various chiral resorcinarene derivatives. The chirality of these compounds results from their structure (the axial chirality) or from the presence of chiral auxiliaries. Moreover, the synthesis of chiral resorcinarene derivatives from chiral substrates is also possible. In this short review, we wish to present the strategies and methodology of the synthesis of chiral resorcinarenes, treating this article as an introduction to the chirality of resorcinarenes.

1 February 2006 in Tetrahedron
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Journal Article
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MUMariusz Urbaniak
Mariusz Urbaniak
WIWaldemar Iwanek
Waldemar Iwanek