Karel František WiesnerFRSFRSCOC (November 25, 1919 – November 28, 1986) was a Canadian chemist of Czech origin known for his contributions to the chemistry of natural products, notably aconitumalkaloids and digitalisglycosides.[1][2]
Early life and career
He was born in Prague, Czechoslovakia, into a family of some wealth and notability. His undergraduate education began in 1938 when he enrolled to study natural sciences at Charles University. His studies were interrupted the following year when universities were shuttered under the German occupation. Working under the supervision of Rudolf Brdička [cz] at Bulovka Hospital, and in a rudimentary laboratory in the basement of his parental home, he discovered a polarographic method of measuring fast chemical reactions. He was awarded a doctorate for this research when Charles University reopened in 1945.[1][3]
In 1943, he joined a research group at the Fragner pharmaceutical company near Prague that was working to develop a penicillin variant. Despite working in secrecy and isolation under onerous wartime restrictions, the group managed to first separate and then test an antimicrobial drug.[4] Wiesner's role included ensuring an adequate supply of the antibiotic by extracting and purifying the substance from the test subject's urine following treatment.[1]
From 1946 until 1948 he conducted postgraduate research in organic chemistry under Vladimir Prelog at ETH, Zürich, funded by a Rockefeller fellowship. Wiesner immigrated to Canada in 1948 to take up a position at the University of New Brunswick, Fredericton. Apart from a two-year spell with the pharmaceutical company Ayerst in Montreal, he remained at UNB for the remainder of his career. In 1981, Wiesner became a founding member of the World Cultural Council.[5] He died of lymphoma in 1986.[1]
Scientific achievements
Wiesner made remarkable contributions to the structural and synthetic chemistry of complex polysubstituted polycyclic natural products. In the 1950s, prior to the development of nuclear magnetic resonancespectroscopy, he determined the structure of several diterpene alkaloids including veatchine, atisine, annotinine, delphinine, aconitine, and songorine. After returning to New Brunswick from Ayerst in 1964, he began a successful program to synthesize these compounds, culminating in the total synthesis of chasmanine and napelline. Towards the end of the 1970s Wiesner turned his attention to digitalis derivatives, with the goal of finding cardiac glycosides with safer therapeutic ratios. In the last decade of his career he succeeded in demonstrating the separation of the inotropic and toxic properties of this group of compounds, elucidated the underlying chemical mechanism, and finally achieved the total synthesis of digitoxin and other cardioactive steroids.[1]
^ abcdeSchneider, W.G.; Valenta, Z. (1991). "Karel František Wiesner. 25 November 1919 – 28 November 1986". Biographical Memoirs of Fellows of the Royal Society. 37: 462–490. doi:10.1098/rsbm.1991.0024. JSTOR770040.
^Brossi, Arnold, ed. (1987). The Alkaloids: Chemistry and Pharmacology. Vol. 30 (1st ed.). London: Academic Press. ISBN978-0-08-086554-6. OCLC505149410.
^Wiesner, Karel (1977). "Centenary lecture. Systematic development of strategy in the synthesis of polycyclic polysubstituted natural products: the aconite alkaloids". Chemical Society Reviews. 6 (4). Royal Society of Chemistry (RSC): 413. doi:10.1039/cs9770600413. ISSN0306-0012.
^"Deceased Academicians". Pontifical Academy of Sciences. August 5, 1950. Retrieved March 22, 2019.
