A facile synthesis of N-carbamoylmethyl-α-aminobutyrolactones by the Ugi multicomponent condensation reaction

Tetrahedron Letters

Volumn 39, Issue 39, 1998, Pages 7109-7112

  Park, Soo Jung ^a   Keum, Gyochang ^a   Kang, Soon Bang ^a   Koh, Hun Yeong ^a   Kim, Youseung ^a   Duck Hyung, Lee ^b  

^a Korea Institute of Science and Technology   (South Korea)

^b Sogang University   (South Korea)

Author keywords

Amino acids and derivatives; Condensations; Lactones; Ugi Passerini reactions

Indexed keywords

LACTONE; N CARBAMOYLMETHYL ALPA AMINOBUTYROLACTONE; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATION; MOLECULAR INTERACTION; POLYMERIZATION; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0032563923     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01509-3     Document Type: Article

References (25)

1. [1] Gallop MA, Barrett RW, Dower WJ, Fodor SPA, Gordon EM. J. Med. Chem. 1994;37:1233-1251.
2. [2] Gordon EM, Barrett RW, Dower WJ, Fodor SPA, Gallop MA. J. Med. Chem. 1994;37:1385-1401.
3. [3] Thompson LA, Ellman JA. Chem. Rev. 1996;96:555-600.
4. [4] Balkenhohl F, Bussche-Hunnefeld C, Lansky A, Zechel C. Angew. Chem. Int. Ed. Engl., 1996;35:2288-2337.
5. [5] Ugi I. Proc. Estonian Acad. Sci. Chem. 1995;44(4):237-273.
6. [6] Armstrong RW, Combs AP, Tempest PA, Brown SD, Keating TA. Acc. Chem. Res. 1996;29:123-131.
7. [7] Ugi I, Lohberger S, Karl R. In Comprehensive Organic Synthesis; Trost BM, Fleming I, Eds.; Pergamon: New York, 1991;2:1083-1109.
8. [8] Ugi I. Angew. Chem. Int. Ed. Engl. 1962;1:8-21.
9. [9] Ugi I. Angew. Chem. Int. Ed. Engl. 1982;21:810-819.
10. [10] Keating TA, Armstrong RW. J. Org. Chem. 1998;63:867-871
11. [11] Mjalli AMM, Short KM. Tetradron Lett. 1997;38(3):359-362.
12. [12] Harriman GCB. Tetrahedron Lett. 1997;38(32):5591-5594.
13. [13] Hanusch-Kompa C, Ugi I. Tetrahedron Lett. 1998;39:2725-2728.
14. [14] Pitlik J, Townsend CA. Bioorg. Med. Chem. Lett. 1997;7(24):3129-3134.
15. [15] Short KM, Ching BW, Mjalli AMM. Tetrahedron, 1997;53(19):6653-6679.
16. [16] Short KM, Ching BW, Mjalli AMM. Tetrahedron Lett. 1996;37(42):7489-7492.
17. [17] Bienayme H, Bouzid K. Tetrahderon Lett. 1998;39:2735-2738.
18. [18] Zhang C, Moran EJ, Woiwode TF, Short KM, Mjalli AMM. Tetrahedron Lett. 1996;37(6):751-754.
19. [19] Strocker AM, Keating TA, Tempest PA, Armstrong RW. Tetrahedron Lett. 1996;37(42):1149-1152.
20. [20] Keating TA, Armstrong RW. J. Am. Chem. Soc. 1996;118:2574-2583.
21. [21] Mjalli AMM, Sarshar S, Baiga TJ. Tetrahedron Lett. 1996;37(17):2943-2946.
22. [22] Keating TA, Armstrong RW. J. Org. Chem. 1996;61:8935-8939.
23. [23] Hulme C, Morrissette MM, Volz FA, Burns CJ. Tetrahedron Lett. 1998;39:1113-1116.
24. [24] Ko D, Kim DJ, Lyn CS, Min IK, Moon H. Tetrahedron Lett. 1998;39:297-300.
25. [25] Telford G, Wheeler D, Williams P, Tomkins PT, Appleby P, Sewell H, Stewart GSAB, Bycroft BW, Pritchard D I. Infection and Immunity, 1998;66:36-42.