MeOTf-induced carboannulation of arylnitriles and aromatic alkynes: a new metal-free strategy to construct indenones-Reference-Cited by-同舟云学术

MeOTf-induced carboannulation of arylnitriles and aromatic alkynes: a new metal-free strategy to construct indenones

Published:2014 Issue:21 Volume:50 Page:2775-2777
ISSN:1359-7345
Container-title:Chem. Commun.
language:en
Short-container-title:Chem. Commun.

Author:

Yan Xiaoyu¹²³⁴,Zou Song⁵⁶⁷,Zhao Peng¹²³⁴,Xi Chanjuan¹²³⁴⁸

Affiliation:

1. Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology (Ministry of Education)

2. Department of Chemistry

3. Tsinghua University

4. Beijing 100084, China

5. School of Pharmaceutical Science

6. Jiangnan University

7. Wuxi 214122, China

8. State Key Laboratory of Elemento-Organic Chemistry

Abstract

MeOTf-induced carboannulation of arylnitriles and aromatic alkynes for synthesis of indenones and their derivatives under metal-free conditions has been described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC00088A

Reference38 articles.

1. A Catalytic Enantioselective Synthesis of the Endothelin Receptor Antagonists SB-209670 and SB-217242. A Base-Catalyzed Stereospecific Formal 1,3-Hydrogen Transfer of a Chiral 3-Arylindenol

2. Concise Synthesis of Pauciflorol F Using a Larock Annulation

3. Total Synthesis of Isoprekinamycin: Structural Evidence for Enhanced Diazonium Ion Character and Growth Inhibitory Activity toward Cancer Cells

4. Synthesis of Substituted Naphthalenes via a Catalytic Ring-Expansion Rearrangement

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