ESTONIAN ACADEMY
PUBLISHERS
eesti teaduste
akadeemia kirjastus
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Proceedings of the Estonian Academy of Sciences. Chemistry
Chemistry of the isocyanides and their multicomponent reactions, including their libraries – the initiatives of Ivar Ugi; pp. 98–102
PDF | https://doi.org/10.3176/chem.2007.2.05

Author
Mihkel Veiderma
References

1. Ugi, I. Isonitrile Chemistry. Academic Press, New York, 1971.

2. Ugi, I. Perspektiven von Multikomponentenreaktionen und ihren Bibliotheken. J. Prakt. Chem., 1997, 339, 499–516.
https://doi.org/10.1002/prac.19973390193

3. Ugi, I. & Meyr, R. Neue Darstellungsmethode für Isonitrile. Angew. Chem., 1958, 70, 702–703.
https://doi.org/10.1002/ange.19580702213

4. Ugi, I., Meyr, R., Fetzer, U. & Steinbrückner, C. Versuche mit Isonitrilen. Angew. Chem., 1959, 71, 386.

5. Ugi, I., Lohberger, S. & Karl, R. The Passerini and Ugi reactions. In Comprehensive Organic Synthesis: Selectivity for Synthetic Efficiency (Trost, B. M. & Heathcock, C. H., eds). Pergamon, Oxford, 1991, Vol. 2, Chap. 4, 6.
https://doi.org/10.1016/B978-0-08-052349-1.00057-3

6. Dömling, A. & Ugi, I. Multikomponentreaktionen mit Isocyaniden. Angew. Chem., 2000, 112, 3300–3344; Multicomponent reactions with isocyanides. Angew. Chem. Int. Ed. Engl., 2000, 39, 3168–3210.
https://doi.org/10.1002/1521-3757(20000915)112:18<3300::AID-ANGE3300>3.0.CO;2-Z
https://doi.org/10.1002/1521-3773(20000915)39:18<3168::AID-ANIE3168>3.0.CO;2-U

7. Ugi, I. & Offermann, K. Asymmetrische 1,3-Induktion by der a-Addition von Immonium-Ionen und Carboxylat-Anionen an Isonitrile. Angew. Chem., 1963, 75, 917; Angew. Chem. Int. Ed. Engl., 1963, 2, 624.
https://doi.org/10.1002/ange.19630751907

https://doi.org/10.1002/anie.196306242

8. Ugi, I. & Kaufhold, G. Stereoselektive Synthesen IV. Der Reaktionsmechanismus stereo­selektiver Vierkomponenten-Kondensationen. Liebigs Ann. Chem., 1967, 709, 11–28.
https://doi.org/10.1002/jlac.19677090103

9. Ugi, I., Marquarding, D. & Urban, R. Syntheses of peptides by four-component condensation. In Chemistry and Biochemistry of Amino Acids. Peptides and Proteins, Vol. 6 (Wein­stein, B., ed.). Marcel Dekker, New York, 1982, 245–289.

10. Kunz, H. & Pfrengle, W. Asymmetric synthesis on carbohydrate templates: stereoselective Ugi-synthesis of a-amino acid derivatives. J. Am. Chem. Soc., 1988, 110, 651–652.
https://doi.org/10.1021/ja00210a084

11. Kunz, H. & Pfrengle, W. Carbohydrates as chiral templates: asymmetric Ugi-synthesis of alpha-amino acids using galactosylamines as the chiral matrices. Tetrahedron, 1988, 44, 5487–5494.
https://doi.org/10.1016/S0040-4020(01)86054-3

12. Dömling, A. & Ugi, I. Die Sieben-Komponenten-Reaktion. Angew. Chem., 1993, 105, 634–635; The seven-component reaction. Angew. Chem. Int. Ed. Engl., 1993, 32, 563–564.
https://doi.org/10.1002/ange.19931050440

13. Ugi, I., Dömling, A. & Hörl, W. Multicomponent reactions in organic chemistry. Endeavour, 1994, 18, 115–122.
https://doi.org/10.1016/S0160-9327(05)80086-9

14. Ugi, I., Dömling, A. & Hörl, W. Multikomponentreaktionen. GIT Fachzeitschr. Labor., 1994, 38, 430–437.

15. Ugi, I., Ebert, B. & Hörl, W. Formation of 1,1’-iminodicarboxylic acid derivatives, 2,6-diketo-piperazine and dibenzodiazocine-2,6-dione by variations of multicomponent reactions. Chemosphere, 2001, 43, 75–81.
https://doi.org/10.1016/S0045-6535(00)00326-X

16. Ugi, I. & Steinbrückner, C. Isonitrile II. Reaktion von Isonitrilen mit Carbonylverbindungen, Aminen und Stickstoffwasserstoffsäure. Chem. Ber., 1961, 94, 734–742.
https://doi.org/10.1002/cber.19610940323

17. Furka, A. History of combinatorial chemistry. Drug Dev. Res., 1995, 36, 1–12.
https://doi.org/10.1002/ddr.430360102

18. Rossen, K., Pye, P. J., DiMichele, L. M., Volante, R. P. & Reider, P. J. An efficient asymmetric hydrogenation approach to the synthesis of the Crixivan® piperazine intermediate. Tetra­hedron Lett., 1998, 39, 6823–6826.
https://doi.org/10.1016/S0040-4039(98)01484-1

19. Weber, L., Waltbaum, S., Broger, C. & Gubernator, K. Optimisierung der biologischen Aktivität von kombinatorischen Verbindungsbibliotheken durch einen genetischen Algo­rithmus. Angew. Chem., 1995, 107, 2452–2454; Optimization of the biological activity of combinatorial compound libraries by a genetic algorithm. Angew. Chem. Int. Ed. Engl., 1995, 34, 2280–2282.
https://doi.org/10.1002/ange.19951072025
https://doi.org/10.1002/anie.199522801

 

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