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Total Synthesis of Mucronin B

1983; Wiley; Volume: 22; Issue: 2 Linguagem: Inglês

10.1002/anie.198301521

1521-3773

Ulrich Schmidt, Ute Schanbacher,

Biochemical and Structural Characterization

Angewandte Chemie International Edition in EnglishVolume 22, Issue 2 p. 152-153 Communication Total Synthesis of Mucronin B† Prof. Dr. Ulrich Schmidt, Corresponding Author Prof. Dr. Ulrich Schmidt Institut für Organische Chemie der Universität, Pfaffenwaldring 55, D-7000 Stuttgart 80 (Germany)Institut für Organische Chemie der Universität, Pfaffenwaldring 55, D-7000 Stuttgart 80 (Germany)Search for more papers by this authorUte Schanbacher, Ute Schanbacher Institut für Organische Chemie der Universität, Pfaffenwaldring 55, D-7000 Stuttgart 80 (Germany)Search for more papers by this author Prof. Dr. Ulrich Schmidt, Corresponding Author Prof. Dr. Ulrich Schmidt Institut für Organische Chemie der Universität, Pfaffenwaldring 55, D-7000 Stuttgart 80 (Germany)Institut für Organische Chemie der Universität, Pfaffenwaldring 55, D-7000 Stuttgart 80 (Germany)Search for more papers by this authorUte Schanbacher, Ute Schanbacher Institut für Organische Chemie der Universität, Pfaffenwaldring 55, D-7000 Stuttgart 80 (Germany)Search for more papers by this author First published: February 1983 https://doi.org/10.1002/anie.198301521Citations: 25 † Synthesis of Peptide Alkaloids, Part 8; Amino Acids and Peptides, Part 40. This work was supported by the Fonds der Chemischen Industrie, BASF AG, and the Deutsche Forschungsgemeinschaft. Dr. W. Rozdzinski is thanked for numerous mass spectra and Prof. Dr. K.-D. Jany for the determinations of allo-isoleucine. Degussa AG is thanked for a generous gift of amino acids and noble metal catalysts.—Part 7: Liebigs Ann. Chem., in press; Part 39: Angew. Chem., in press. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1 Review: R. Tschesche, E. K. Kaussmann in R. H. Manske: The Alkaloids, Vol. 15, Academic Press, New York 1975. 2(a) U. Schmidt, A. Lieberknecht, H. Bökens, H. Griesser, Angew. Chem. 93 (1981) 1121; Angew. Chem. Int. Ed. Engl. 20 (1981) 1026; (b) U. Schmidt, A. Lieberknecht, U. Schanbacher, Th. Beuttler, J. Wild, Angew. Chem. Int. Ed. Engl. 94 (1982) 797; Angew. Chem. Int. Ed. Engl. 21 (1982) 770; Angew. Chem. Suppl. 1982, 1682; example 6d; (c) U. Schmidt, A. Lieberknecht, H. Griesser, J. Talbiersky, Angew. Chem. 93 (1981) 271; Angew. Chem. Int. Ed. Engl. 20 (1981) 280; J. Org. Chem. 47 (1982) 3261. 3 H.-W. Fehlhaber, J. Uhlendorf, S. T. David, R. Tschesche, Liebigs Ann. Chem. 759 (1972) 195. 4 In compounds 8–10 a mixture of four diastereomers is present in each case. The spatial arrangement at the benzyl site and at the Ile side-chain is not, however, considered in the designation. 5 J. C. Lagarias, R. A. Houghten, H. Rapoport, J. Am. Chem. Soc. 100 (1978) 8202; D. Goff, J. C. Lagarias, W. C. Shih, M. P. Klein, H. Rapoport, J. Org. Chem. 45 (1980) 4813; F. Rocchiccioli, F. X. Jarreau, M. Pais, Tetrahedron 34 (1978) 2917. Citing Literature Volume22, Issue2February 1983Pages 152-153 ReferencesRelatedInformation