Selective Formation of Mono- and Tetra-Cycloadducts by the Diels-Alder Reaction of [60]fullerene with 2,5-Dimethylthiophene S-Oxides

He-ping Zeng; Shoji Eguchi

doi:10.1055/s-1997-747

Subscribe to RSS

Please copy the URL and add it into your RSS Feed Reader.

https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml

Share / Bookmark

Facebook Linkedin Weibo

Download PDF

Synlett 1997; 1997(2): 175-176
DOI: 10.1055/s-1997-747

letter

© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Selective Formation of Mono- and Tetra-Cycloadducts by the Diels-Alder Reaction of [60]fullerene with 2,5-Dimethylthiophene S-Oxides

He-ping Zeng¹ , Shoji Eguchi²

¹Department of Chemistry, South China Normal University, Guangzhou 510631, P.R. China
²Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-01, Japan, Fax +81(52)789-3199; E-mail: eguchi@apchem.nagoya-u.ac.jp

Further Information

Publication History

Publication Date:
31 December 2000 (online)

PDF Download Permissions and Reprints All articles of this category

2,5-Dimethylthiophene S-monoxide and S,S-dioxide prepared from the corresponding thiophene by BF₃-Et₂O catalyzed oxidation with m-CPBA reacted with fullerene C₆₀ at room temperature to produce specifically mono- and tetra-adduct respectively.

thiophene S-oxides - Diels-Alder reaction - [60]fullerene