Ulrich Jordis

Affiliations: 
1972-2013 Inst. Organic Chemistry TU Vienna 
Area:
Heterocyclic Chemistry, natural product synthesis
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"Ulrich Jordis"
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Parents

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Fritz Sauter grad student 1971-1974
 (Habilitation)
Sidney M. Hecht post-doc 1975-1976 MIT
Nelson J. Leonard post-doc 1983-1983 UIUC

Children

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Atul Manvar grad student TU Vienna
Manfred Rudolf grad student 1983-1985 TU Vienna
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Publications

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Fröhlich H, Gärtner P, Jordis U, et al. (2020) Nachruf auf Prof. Fritz Sauter (1930 – 2020) Nachrichten Aus Der Chemie. 68: 97-97
Khan FA, Rabong C, Jordis U, et al. (2013) Surprising behavior of NXO-peptides toward the lithium hydroxide solvolysis Tetrahedron Letters. 54: 3679-3682
Stanetty C, Wolkerstorfer A, Amer H, et al. (2012) Synthesis and antiviral activities of spacer-linked 1-thioglucuronide analogues of glycyrrhizin. Beilstein Journal of Organic Chemistry. 8: 705-11
Amer H, Mereiter K, Stanetty C, et al. (2010) Synthesis and crystal structures of ring A modified glycyrrhetinic acid derivatives derived from 2,3-oxirane and 2,3-thiirane intermediates Tetrahedron. 66: 4390-4402
JORDIS U, SAUTER F, SIDDIQI SM. (2010) ChemInform Abstract: Synthesis of (1R,4S,5R)-endo-N,N-Dimethyl-2-azabicyclo(2.2.1) methanamine. Cheminform. 23: no-no
SAUTER F, STANETTY P, SCHULNER J, et al. (2010) ChemInform Abstract: Fungicidal Pyridine Derivatives. Part 2. Derivates of α- Trichloromethyl-3-pyridinemethanol. Cheminform. 23: no-no
JORDIS U, SAUTER F, BURKART M, et al. (2010) ChemInform Abstract: Synthesis of Novel Quinolone-Chemotherapeutics. Part 5. Methodical Investigations on the Synthesis of Quinolone Chemotherapeutics. Cheminform. 23: no-no
SAUTER F, JORDIS U, MARTINEK P, et al. (2010) ChemInform Abstract: A New Synthesis of Benzo(b)naphtho(2,3-d)thiophenes. Cheminform. 22: no-no
del Ruiz Ruiz MC, Amer H, Stanetty C, et al. (2009) Efficient synthesis of glycyrrhetinic acid glycoside/glucuronide derivatives using silver zeolite as promoter. Carbohydrate Research. 344: 1063-71
Rabong C, Valla C, Kartsev VG, et al. (2007) Stereochemical outcome of the T-reaction employing chiral bicyclic amines Mendeleev Communications. 17: 318-320
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