Sumanene derivatives functionalized at the internal carbon-Reference-Cited by-同舟云学术

Sumanene derivatives functionalized at the internal carbon

Published:2017 Issue:4 Volume:53 Page:697-700
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Ngamsomprasert Niti¹²³⁴,Dang Jing-Shuang¹²³⁴,Higashibayashi Shuhei⁵⁶⁷⁴,Yakiyama Yumi¹²³⁴,Sakurai Hidehiro¹²³⁴

Affiliation:

1. Division of Applied Chemistry Graduate School of Engineering

2. Osaka University

3. Osaka 565-0871

4. Japan

5. Research Center of Integrative Molecular Systems

6. Institute for Molecular Science

7. Okazaki 444-8787

Abstract

The first internal functionalization of sumanene.

Funder

Japan Science and Technology Agency

Ministry of Education, Culture, Sports, Science, and Technology

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/2017/CC/C6CC08970D

Reference33 articles.

1. Structural Reassignment of the Mono- and Bis-Addition Products from the Addition Reactions of N-(Diphenylmethylene)glycinate Esters to [60]Fullerene under Bingel Conditions

2. Synthesis of [60]Fullerene Adducts Bearing Carbazole Moieties by Bingel Reaction and Their Properties

3. Retrocyclopropanation Reactions of Fullerenes: Complete Product Analyses

4. Efficient cyclopropanation of C60 starting from malonates

5. Cyclopropanierung von Fullerenen

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