Abstract
Retinoic acid analogs containing an aromatic ring fixed between the 5 and 8 positions of retinoic acid, were synthesized by a palladium-catalyzed cross-coupling reaction between boronic acid and an alkenyltriflate or alkenyliodide. The biological activities of the retinoic acid analogs were evaluated.
Keywords: Heteroarotinoid, Boronic acid, Coupling reaction, RAR, RXR
Letters in Drug Design & Discovery
Title: Preparation and Biological Activities of Heteroarotinoids
Volume: 4 Issue: 6
Author(s): Akimori Wada, Yukari Mizuguchi, Hiromi Miyake, Miki Niihara, Masayoshi Ito, Kimie Nakagawa and Toshio Okano
Affiliation:
Keywords: Heteroarotinoid, Boronic acid, Coupling reaction, RAR, RXR
Abstract: Retinoic acid analogs containing an aromatic ring fixed between the 5 and 8 positions of retinoic acid, were synthesized by a palladium-catalyzed cross-coupling reaction between boronic acid and an alkenyltriflate or alkenyliodide. The biological activities of the retinoic acid analogs were evaluated.
Export Options
About this article
Cite this article as:
Akimori Wada , Yukari Mizuguchi , Hiromi Miyake , Miki Niihara , Masayoshi Ito , Kimie Nakagawa and Toshio Okano , Preparation and Biological Activities of Heteroarotinoids, Letters in Drug Design & Discovery 2007; 4 (6) . https://dx.doi.org/10.2174/157018007781387827
DOI https://dx.doi.org/10.2174/157018007781387827 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers