Diversity-oriented synthesis of tetrathia[8]circulenes by sequential C–H borylation and annulation-Reference-Cited by-同舟云学术

Diversity-oriented synthesis of tetrathia[8]circulenes by sequential C–H borylation and annulation

Published:2015 Issue:95 Volume:51 Page:16944-16947
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kato Shohei¹²³⁴⁵,Serizawa Yuma¹²³⁴⁵,Sakamaki Daisuke⁶²⁷⁸⁵,Seki Shu⁶²⁷⁸⁵^ORCID,Miyake Yoshihiro¹²³⁴⁵,Shinokubo Hiroshi¹²³⁴⁵

Affiliation:

1. Department of Applied Chemistry

2. Graduate School of Engineering

3. Nagoya University

4. Nagoya 464-8603

5. Japan

6. Department of Molecular Engineering

7. Kyoto University

8. Nishikyo-ku

Abstract

We have succeeded in the diversity-oriented synthesis of tetrathia[8]circulenes by sequential C–H borylation and annulation from cyclic tetrathiophene.

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/2015/CC/C5CC06921A

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