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AuthorPallikonda G.
AuthorHsieh C.-Y.
AuthorSu H.-L.
AuthorHsieh J.-C.
Available date2020-04-01T09:45:58Z
Publication Date2019
Publication NameResearch on Chemical Intermediates
ResourceScopus
ISSN9226168
URIhttp://dx.doi.org/10.1007/s11164-019-03977-z
URIhttp://hdl.handle.net/10576/13730
AbstractThree related alkaloids, oxynitidine, nitidine and 5,6-dihydronitidine, have been afforded by the new synthetic protocols. In this approach, the Ni-catalyzed annulation reaction is indicated as the key step to construct the isoquinolinone core structure. The subsequent transformations lead to the target alkaloids. - 2019, Springer Nature B.V.
SponsorWe thank the Ministry of Science and Technology of Taiwan (ROC) for the financial support of this research (MOST 107-2113-M-032-006) and the fellowship for Gangaram Pallikonda (MOST 107-2811-M-032-002). Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Languageen
PublisherSpringer Netherlands
Subject5, 6-Dihydronitidine
Alkaloids
Benzo[c]phenanthridine
Nitidine
Oxynitidine
TitleA combined pathway for the synthesis of nitidine family alkaloids
TypeArticle
Pagination5399-5407
Issue Number11
Volume Number45
dc.accessType Abstract Only


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