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  1. Article: Synthetic Studies Toward the Skyllamycins: Total Synthesis and Generation of Simplified Analogues

    Giltrap, Andrew M / F. P. Jake Haeckl / Kenji L. Kurita / Richard J. Payne / Roger G. Linington

    Journal of organic chemistry. 2018 May 25, v. 83, no. 13

    2018  

    Abstract: Herein, we report our synthetic studies toward the skyllamycins, a highly modified class of nonribosomal peptide natural products which contain a number of interesting structural features, including the extremely rare α-OH-glycine residue. Before ... ...

    Abstract Herein, we report our synthetic studies toward the skyllamycins, a highly modified class of nonribosomal peptide natural products which contain a number of interesting structural features, including the extremely rare α-OH-glycine residue. Before embarking on the synthesis of the natural products, we prepared four structurally simpler analogues. Access to both the analogues and the natural products first required the synthesis of a number of nonproteinogenic amino acids, including three β-OH amino acids that were accessed from the convenient chiral precursor Garner’s aldehyde. Following the preparation of the suitably protected nonproteinogenic amino acids, the skyllamycin analogues were assembled using a solid-phase synthetic route followed by a final stage solution-phase cyclization reaction. To access the natural products (skyllamycins A–C) the synthetic route used for the analogues was modified. Specifically, linear peptide precursors containing a C-terminal amide were synthesized via solid-phase peptide synthesis. After cleavage from the resin the N-terminal serine residue was oxidatively cleaved to a glyoxyamide moiety. The target natural products, skyllamycins A–C, were successfully prepared via a final step cyclization with concomitant formation of the unusual α-OH-glycine residue. Purification and spectroscopic comparison to the authentic isolated material confirmed the identity of the synthetic natural products.
    Keywords aldehydes ; cyclization reactions ; moieties ; organic chemistry ; serine ; spectroscopy
    Language English
    Dates of publication 2018-0525
    Size p. 7250-7270.
    Publishing place American Chemical Society
    Document type Article
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021/acs.joc.8b00898
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: The Natural Products Atlas

    Jeffrey A. van Santen / Grégoire Jacob / Amrit Leen Singh / Victor Aniebok / Marcy J. Balunas / Derek Bunsko / Fausto Carnevale Neto / Laia Castaño-Espriu / Chen Chang / Trevor N. Clark / Jessica L. Cleary Little / David A. Delgadillo / Pieter C. Dorrestein / Katherine R. Duncan / Joseph M. Egan / Melissa M. Galey / F.P. Jake Haeckl / Alex Hua / Alison H. Hughes /
    Dasha Iskakova / Aswad Khadilkar / Jung-Ho Lee / Sanghoon Lee / Nicole LeGrow / Dennis Y. Liu / Jocelyn M. Macho / Catherine S. McCaughey / Marnix H. Medema / Ram P. Neupane / Timothy J. O’Donnell / Jasmine S. Paula / Laura M. Sanchez / Anam F. Shaikh / Sylvia Soldatou / Barbara R. Terlouw / Tuan Anh Tran / Mercia Valentine / Justin J. J. van der Hooft / Duy A. Vo / Mingxun Wang / Darryl Wilson / Katherine E. Zink / Roger G. Linington

    ACS Central Science, Vol 5, Iss 11, Pp 1824-

    An Open Access Knowledge Base for Microbial Natural Products Discovery

    2019  Volume 1833

    Keywords Chemistry ; QD1-999
    Language English
    Publishing date 2019-11-01T00:00:00Z
    Publisher American Chemical Society
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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