Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth‐Generation Rhodium Catalytic System-Reference-Cited by-同舟云学术

Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth‐Generation Rhodium Catalytic System

Published:2015-08-27 Issue:40 Volume:21 Page:13883-13887
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Loh Charles C. J.¹,Fang Xiang¹²,Peters Brendan¹,Lautens Mark¹

Affiliation:

1. Department of Chemistry, Davenport Chemical Laboratories, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6 (Canada)

2. Laboratory for Advanced Material and Institute of Fine Chemicals, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237 (P. R. China)

Funder

Solvias AG, Umicore

National Sciences and Engineering Research Council

Deutsche Forschungsgemeinschaft

National Natural Science Foundation of China

China Scholarship Council

NSERC

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201502718

Reference82 articles.

1. For examples utilizing anthrones as anti‐tubulin agents see:

2. Novel Benzylidene-9(10H)-anthracenones as Highly Active Antimicrotubule Agents. Synthesis, Antiproliferative Activity, and Inhibition of Tubulin Polymerization

3. 10-(2-oxo-2-Phenylethylidene)-10H-anthracen-9-ones as Highly Active Antimicrotubule Agents: Synthesis, Antiproliferative Activity, and Inhibition of Tubulin Polymerization

4. Antitubulin agents for the treatment of cancer – a medicinal chemistry update

5. For examples utilizing anthrones as anti‐inflammatory agents see:

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