| Literature DB >> 27791373 |
Eun-Kyung Jung1, Lisa I Pilkington1, David Barker1.
Abstract
The enantioselective synthesis of 2,3-disubstituted benzomorpholines, analogues of 1,4-benzodioxane natural products, has been achieved via addition of electron-rich aromatic donors to acyl-iminium ions derived from benzomorpholine aminols. Subsequent modification of the benzomorpholine scaffold allows side chains mimicking those found in 1,4-benzodioxane lignans to be added. Antiproliferative testing of the prepared analogues showed promising results against MDA-MB-231 and HCT116 cancer cell lines.Entities:
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Year: 2016 PMID: 27791373 DOI: 10.1021/acs.joc.6b02265
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354