Convenient Syntheses of Benzo-Fluorinated Dibenz[b,f]azepines: Rearrangements of Isatins, Acridines, and Indoles-Reference-Cited by-同舟云学术

Convenient Syntheses of Benzo-Fluorinated Dibenz[b,f]azepines: Rearrangements of Isatins, Acridines, and Indoles

Published:2011-09-22 Issue:20 Volume:13 Page:5592-5595
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Elliott Emma-Claire¹,Bowkett Elizabeth R.¹,Maggs James L.¹,Bacsa John¹,Park B. Kevin¹,Regan Sophie L.¹,O’Neill Paul M.¹,Stachulski Andrew V.¹

Affiliation:

1. Robert Robinson Laboratories, Department of Chemistry, University of Liverpool, Liverpool L69 7ZD, U.K., and MRC Centre for Drug Safety Science, Institute of Translational Medicine, University of Liverpool, Ashton Street, Liverpool, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol202318w

Reference34 articles.

1. The Merck Index,13thed;Merck & Co.:Boca Raton, 2001; p298;

2. Schindler, W. (Geigy AG) US Patent 2,948,718, 1960.

3. An investigation of the formation of cytotoxic, protein-reactive and stable metabolites from carbamazepine in vitro

4. The metabolism of carbamazepine in humans: steric course of the enzymic hydrolysis of the 10,11-epoxide

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