Literature DB >> 20939604

Total synthesis of incednam, the aglycon of incednine.

Takashi Ohtani1, Shinya Tsukamoto, Hiroshi Kanda, Kensuke Misawa, Yoshifumi Urakawa, Takahiro Fujimaki, Masaya Imoto, Yoshikazu Takahashi, Daisuke Takahashi, Kazunobu Toshima.   

Abstract

The first total synthesis of incednam (1), the aglycon of antibiotic incednine (2), is described. Incednine has been reported to exhibit significant inhibitory activity against the antiapoptotic oncoproteins Bcl-2 and Bcl-xL. The synthesis of 1 commenced with the preparation of the C1-C13 subunit 3 and the C14-C23 subunit 4. The construction of the novel 24-membered macrocycle was achieved by the application of a Stille coupling between 3 and 4, followed by macrolactamization.

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Year:  2010        PMID: 20939604     DOI: 10.1021/ol102400c

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Stereoselective synthesis of the disaccharide unit of incednine.

Authors:  Jason R Abbott; William R Roush
Journal:  Org Lett       Date:  2012-12-18       Impact factor: 6.005

2.  Iridium-Catalyzed Enantioselective Allylic Substitution of Enol Silanes from Vinylogous Esters and Amides.

Authors:  Ming Chen; John F Hartwig
Journal:  J Am Chem Soc       Date:  2015-10-23       Impact factor: 15.419

3.  Searching for Glycosylated Natural Products in Actinomycetes and Identification of Novel Macrolactams and Angucyclines.

Authors:  Mónica G Malmierca; Lorena González-Montes; Ignacio Pérez-Victoria; Carlos Sialer; Alfredo F Braña; Raúl García Salcedo; Jesús Martín; Fernando Reyes; Carmen Méndez; Carlos Olano; José A Salas
Journal:  Front Microbiol       Date:  2018-01-30       Impact factor: 5.640

  3 in total

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