Literature DB >> 24420412

Structure elucidation and total synthesis of kulkenon.

Gerrit Symkenberg1, Markus Kalesse.   

Abstract

The impressive biological profile of secondary metabolites isolated from strains of Sorangium cellulosum prompted us to initiate synthetic studies on kulkenon, also isolated from Sorangium cellulosum. The synthesis features a syn-selective vinylogous Kobayashi aldol reaction, recently developed by us, and a ring-closing intramolecular Heck reaction as the pivotal transformations. Comparison of the NMR spectra of the authentic and synthetic material revealed that the proposed configuration had to be revised. A combination of molecular modeling and NOE experiments was used to propose the revised configuration, which was confirmed by a new synthesis.
Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Kobayashi aldol reaction; kulkenon; macrolactones; structure elucidation; total synthesis

Mesh:

Substances:

Year:  2014        PMID: 24420412     DOI: 10.1002/anie.201309386

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  3 in total

Review 1.  Total syntheses of the archazolids: an emerging class of novel anticancer drugs.

Authors:  Stephan Scheeff; Dirk Menche
Journal:  Beilstein J Org Chem       Date:  2017-06-07       Impact factor: 2.883

2.  Towards the total synthesis of chondrochloren A: synthesis of the (Z)-enamide fragment.

Authors:  Jan Geldsetzer; Markus Kalesse
Journal:  Beilstein J Org Chem       Date:  2020-04-14       Impact factor: 2.883

3.  The Total Synthesis of Chondrochloren A.

Authors:  Yannick Linne; Elisa Bonandi; Christopher Tabet; Jan Geldsetzer; Markus Kalesse
Journal:  Angew Chem Int Ed Engl       Date:  2021-02-25       Impact factor: 15.336

  3 in total

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