Total synthesis of hamacanthin B class marine bisindole alkaloids
Chemistry of Heterocyclic Compounds, ISSN: 1573-8353, Vol: 56, Issue: 3, Page: 331-338
2020
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Article Description
[Figure not available: see fulltext.] A method for the synthesis of 1-(1H-indol-3-yl)ethane-1,2-diamines, key synthetic precursors of a number of marine alkaloids, has been developed based on the reduction of adducts of O-benzylhydroxylamine and N-protected 3-(2-nitrovinyl)indoles. For the first time, the total synthesis of 6’,6”-didebromohamacanthin B, 6’-debromohamacanthin B, and 6”-debromohamacanthin B, the secondary metabolites of the sponges Spongosorites and Discodermia calyx, was carried out.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85083805187&origin=inward; http://dx.doi.org/10.1007/s10593-020-02664-x; https://link.springer.com/10.1007/s10593-020-02664-x; https://link.springer.com/content/pdf/10.1007/s10593-020-02664-x.pdf; https://link.springer.com/article/10.1007/s10593-020-02664-x/fulltext.html; https://dx.doi.org/10.1007/s10593-020-02664-x; https://link.springer.com/article/10.1007/s10593-020-02664-x
Springer Science and Business Media LLC
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