Further exploration of the heterocyclic diversity accessible from the allylation chemistry of indigo

Further exploration of the heterocyclic diversity accessible from the allylation chemistry of indigo

Diversity-directed synthesis based on the cascade allylation chemistry of indigo, with its embedded 2,2’-diindolic core, has resulted in rapid access to new examples of the hydroxy-8a,13-dihydroazepino[1,2-a:3,4-b']diindol-14(8H)-one skeleton in up to 51% yield. Additionally a derivative of the...

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Bibliographic Details
Main Authors: Alireza Shakoori, John B. Bremner, Mohammed K. Abdel-Hamid, Anthony C. Willis, Rachada Haritakun, Paul A. Keller
Format: Article
Language:English
Published: Beilstein-Institut 2015-04-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
allylation
cascade reactions
indigo
nitrogen heterocycles
rearrangement
Online Access:https://doi.org/10.3762/bjoc.11.54

Internet

https://doi.org/10.3762/bjoc.11.54

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