Contorted aromatics via a palladium-catalyzed cyclopentannulation strategy-Reference-Cited by-同舟云学术

Contorted aromatics via a palladium-catalyzed cyclopentannulation strategy

Published:2016 Issue:18 Volume:4 Page:3963-3969
ISSN:2050-7526
Container-title:Journal of Materials Chemistry C
language:en
Short-container-title:J. Mater. Chem. C

Author:

Bheemireddy Sambasiva R.¹²³⁴,Ubaldo Pamela C.¹²³⁴,Finke Aaron D.⁵⁶⁷,Wang Lichang¹²³⁴,Plunkett Kyle N.¹²³⁴

Affiliation:

1. Department of Chemistry and Biochemistry and the Materials Technology Center

2. Southern Illinois University

3. Carbondale

4. USA

5. Swiss Light Source

6. Paul Scherrer Institute

7. Switzerland

Abstract

A palladium-catalyzed cyclopentannulation provides access to contorted aromatics that afford solubility benefits while maintaining pi–pi stacking motifs.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/TC/C5TC02305J

Reference61 articles.

1. Metal-Catalyzed Annulation Reactions for π-Conjugated Polycycles

2. Synthesis of 9-Alkylidene-9H-fluorenes by a Novel, Palladium-Catalyzed Cascade Reaction of Aryl Halides and 1-Aryl-1-alkynes

3. A New Suzuki−Heck-Type Coupling Cascade: Indeno[1,2,3]-Annelation of Polycyclic Aromatic Hydrocarbons

4. Palladium-Catalyzed Formation of Highly Substituted Naphthalenes from Arene and Alkyne Hydrocarbons

5. 9-Stannafluorenes: 1,4-Dimetal Equivalents for Aromatic Annulation by Double Cross-Coupling

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