Effects of the Linkage Length and Substituents on the Photocycloaddition of Bis(vinylnaphthyl)alkanes toward Naphthalenophanes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/66/2/66_2_598/_pdf
Reference30 articles.
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3. Intramolecular [2+2] Photocycloaddition. 5. Synthetic Methods toward [2.n]-, [3.n]-, and [4.n]Naphthalenophane Skeletons by Using α,ω-Bis(vinylnaphthyl)alkanes
4. Transannular interactions in [2.2] phanes as studied by luminescence and optical detection of magnetic resonance
5. Layered Compounds. XLIII. Syntheses and Properties of [2.2]Naphthaleno-and [2.2]Anthraceno-heterophanes
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Synthesis of silicon-containing macrocyclic compounds by using intramolecular [2+2] photocycloaddition reactions of bis-dimethylsilyl-linked styrenes and stilbenes;Journal of Photochemistry and Photobiology A: Chemistry;2018-09
2. ChemInform Abstract: Intramolecular (2 + 2) Photocycloaddition. Part 17. Effects of the Linkage Length and Substituents on the Photocycloaddition of Bis( vinylnaphthyl)alkanes Toward Naphthalenophanes.;ChemInform;2010-08-20
3. Observation of intramolecular singlet and triplet excimers of tethered naphthalene moieties under the geometric constraints imposed by the host framework of zeolites;Physical Chemistry Chemical Physics;2008
4. Photochemical Synthesis of Cyclophanes;CRC Handbookof Organic Photochemistry and Photobiology, Volumes 1 & 2, Second Edition;2003-09-29
5. Synthesis and Fluorescence Emission Behavior ofanti-[2.3](3,10)Phenanthrenophane: Overlap between Phenanthrene Rings Required for Excimer Formation;Chemistry Letters;2001-10
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