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Zoltan Hajos

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Nationality
  
Hungarian-American

Academic advisor
  
Zoltan Csuros

Fields
  
Organic chemistry

Name
  
Zoltan Hajos

Doctoral advisor
  
Zoltan Csuros


Zoltan Hajos

Born
  
3 March 1926 (age 98) Budapest, Hungary (
1926-03-03
)

Institutions
  
Hoffmann-La Roche, Johnson & Johnson

Alma mater
  
Technical University of Budapest

Known for
  
Organocatalysis, total synthesis of steroids

Education
  
Budapest University of Technology and Economics

Zoltan George Hajos (born 3 March 1926) is a Hungarian-born and trained American organic chemist. Originally an academic in his native Budapest, then an industrial chemist in the pharmaceutical industry, he is known for the Hajos–Parrish–Eder–Sauer–Wiechert reaction (originally named Hajos-Parrish reaction by Claude Agami in 1985).

Contents

Chemistry training

Hajos studied chemistry at the Technical University of Budapest (TU Budapest), in Hungary, completing an M.Sc. in 1947, and his doctoral work under Zoltan Csuros of the Institute of Organic Chemical Technology in 1950.

Early academic career

Hajos remained there until accepting a position as assistant professor in organic chemistry at the TU Budapest in 1948, where he stayed until 1952, then as Lecturer at the University of Veszprem (1952-1953), returning as a Research Associate at the Institute of Organic Chemistry at TU Budapest in 1953. With backlash following the 1956 Revolution in October, 1956, Hajos left TU Budapest and communist Hungary for the United States, where he took a position as a research associate in organic chemistry, a senior postdoctoral-level position, in the Department of Chemistry at Princeton University, beginning in 1957.

Second academic and pharmaceutical periods

Hajos accepted a chemistry position with the Pharmaceutical Research Institute of Hoffmann-La Roche, a pharmaceutical company, in Nutley, New Jersey, in 1960. He remained in that position until beginning a second phase of an academic career in 1970, first in the Chemistry Department of the University of Vermont (1972-1973), and thereafter on the Faculty of Pharmacy of the University of Toronto (1973 -1974). Hajos returned to the pharmaceutical industry in 1975, proceeding through a series of positions at the Research Institute of Johnson & Johnson, until retiring in 1990.

Hajos–Parrish–Eder–Sauer–Wiechert reaction, discovery and importance

Hajos is noted for the Hajos–Parrish–Eder–Sauer–Wiechert reaction, and of the related (S)-proline-catalyzed synthesis route to the Hajos-Wiechert ketone, and is considered a pioneer in the research area of organocatalysis. In a recent review of the Hajos–Parrish–Eder–Sauer–Wiechert reaction as a name reaction, Daniel Zerong Wang describes it, and its synonyms, thus:

"This reaction was independently reported by two groups in 1971: the group of Hajos and Parrish [citing a German patent dated 29 July 1971] and the group of Eder, Sauer, and Wiechert [citing a German patent dated October 7, 1971, and a 1971 journal report in German and English translation]. It is an enantioselective [a]ldol [r]eaction catalyzed by (S)-proline… [and is] one of the earliest enantioselectively catalyzed reactions of practical use in synthetic organic chemistry. Owing to its wide application in organic synthesis, it has been extensively explored and extended to asymmetric [a]ldol... α-alkylation… Mannich... Michael [a]ddition... and α-amination… [reactions] of carbonyl compounds. In the literature, this reaction has been referred to by different names: [as the Hajos–Parrish–Eder–Sauer–Wiechert reaction]... Hajos-Eder-Sauer-Wiechert... Hajos-Wiechert... and Hajos-Parrish-Wiechert reactions."

Benjamin List, a leader in the modern field of organocatalysis, describes the importance of the discovery of the Hajos–Parrish–Eder–Sauer–Wiechert reaction thus:

"Discovered in the early 1970s, the Hajos–Parrish–Eder–Sauer–Wiechert reaction, a proline-catalyzed intramolecular aldol reaction [citing journal articles Hajos & Parrish (1974a) and Eder, Sauer & Wiechert (1971b)], represents not only the first asymmetric aldol reaction invented by chemists but also the first highly enantioselective organocatalytic transformation.

Awards and recognition

Hajos received a Certificate of Merit, an Iron Award, from TU Budapest in May 2013, in recognition of 65 years of professional service.

Selected publications

The research activity of Hajos resulted in 45 scientific publications in technical journals, as well as in more than 30 patents. Some selected publications are:

  • R. Malathi, D. Rajagopal, Z. G. Hajos, S. Swaminathan: "Proline-catalysed asymmetric ketol cyclizations: The template mechanism revisited," Journal of Chemical Sciences, 116 (2004) pp. 159−162, doi:10.1007/BF02708219.
  • Z. G. Hajos, D. R. Parrish: "Asymmetric synthesis of bicyclic intermediates of natural product chemistry," Journal of Organic Chemistry 39 (1974), pp. 1615−1621, doi:10.1021/jo00925a003.
  • Z. G. Hajos, D.R. Parrish: "Synthesis and conversion of 2-methyl-2-(3-oxobutyl)-1,3-cyclopentanedione to the isomeric racemic ketols of the [3.2.1]bicyclooctane and of the perhydroindane series," Journal of Organic Chemistry 39 (1974), pp. 1612−1615, doi:10.1021/jo00925a002.
  • Z. G. Hajos, D. R. Parrish: (+)-(7aS)-7a-METHYL-2,3,7,7a-TETRAHYDRO-1 H-INDENE-1,5-(6H-DIONE). Organic Syntheses, Coll. Vol. 7, 363, doi:10.15227/orgsyn.063.0026.
  • Edward C. Kendall, Zoltan G. Hajos: TETRAHYDRO-3,4-FURANDIONE. I. PREPARATION AND PROPERTIES, J. Am. Chem. Soc. 82 (1960), 3219-3220, doi:10.1021/ja01497a059.
  • Z. G. Hajos, N. Cohen, D. R. Parrish, L. A. Portland, W. Sciamanna, M. A. Scott, P. A. Wehrli, 1975, "Total syntheses of optically active 19-norsteroids: (+)-estr-4-ene-3,17-dione and (+)-13β-ethylgon-4-ene-3,17-dione," Journal of Organic Chemistry 40, pp. 675−681, PMID 1133631.
  • J. B. Press, R. Falotico, Z. G. Hajos, R. A. Sawyers, R. M. Kanojia, L. Williams, B. Haertlein, J. A. Kauffman, C. Lakas-Weiss, J. J. Salata: Synthesis and structure-activity relationship of 6-substituted purine derivatives as novel selective positive inotropes, Journal of Medicinal Chemistry 35 (1992) 4509-4515, doi:10.1021/jm00102a001.
  • References

    Zoltan Hajos Wikipedia