Buckminsterfullerene C60–o-Quinone Methide Cycloadduct
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/22/11/22_11_1833/_pdf
Reference6 articles.
1. Calculations of the ionization thresholds and electron affinities of the neutral, positively and negatively charged C60—‘‘follene‐60’’
2. Isolation of fullerene products from flames: Structure and synthesis of the C60-cyclopentadiene adduct
3. Synthesis of a rigid "ball-and-chain" donor-acceptor system through Diels-Alder functionalization of buckminsterfullerene (C60)
4. [3 + 2] and [4 + 2] Cycloadditions of fullerene C60
5. Reaction of Buckminsterfullerene withortho-Quinodimethane: a New Access to Stable C60Derivatives
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1. Functionalization of Fullerenes: Addition Reactions;Handbook of Fullerene Science and Technology;2022
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3. Synthesis of Fullerotetrahydroquinolines via [4 + 2] Cycloaddition Reaction of [60]Fullerene with in Situ Generated Aza-o-quinone Methides;The Journal of Organic Chemistry;2018-02-05
4. TEMPO-Mediated Synthesis of Tetrahydropyridinofullerenes: Reaction of [60]Fullerene with α-Methyl-Substituted Arylmethanamines and Aldehydes in the Presence of 4-Dimethylaminopyridine;The Journal of Organic Chemistry;2017-12-21
5. Stereoselective Intramolecular Dearomatizative [4+2] Cycloaddition of Linked Ethynylnaphthol-Benzofuran Systems;European Journal of Organic Chemistry;2017-12-08
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