Restricted Rotation Involving the Tetrahedral Carbon. LVI. NMR and Molecular Mechanics Studies on the Stereodynamics of 8,13-Dichloro-9-methoxy-1,4-dimethyltriptycene-Reference-Cited by-同舟云学术

Restricted Rotation Involving the Tetrahedral Carbon. LVI. NMR and Molecular Mechanics Studies on the Stereodynamics of 8,13-Dichloro-9-methoxy-1,4-dimethyltriptycene

Published:1985-06 Issue:6 Volume:58 Page:1690-1695
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Yamamoto Gaku,Oki Michinori

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/58/6/58_6_1690/_pdf

Reference24 articles.

1. Restricted Rotation Involving the Tetrahedral Carbon. LV. Differential Effects of theperi-Substituents on the Rotational Barriers in 9-Ethyl-, 9-Allyl-, and 9-Benzyltriptycenes

2. Unusually High Barriers to Rotation Involving the Tetrahedral Carbon Atom

3. Slow rotation around the benzene-to-oxygen bond in esters of phenols

4. A 4-Phenoxyphenoxy Radical and an Example of Hindered Aryl Ether Rotation

5. A Study of the Barriers to Rotation in Some Highly Substituted Diphenyl Ethers

Cited by 15 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 1,8,13-Substituted Triptycenes;Chemistry Letters;2021-01-05

2. Anthranoxides as Highly Reactive Arynophiles for the Synthesis of Triptycenes;Chemistry – A European Journal;2020-06-11

3. Chemistry of Anthracene–Acetylene Oligomers. XXIII. Molecular Structures and Stereochemistry of Anthracene–Diacetylene Cyclic Dimers Having Two Intraannular Alkoxy Groups;Bulletin of the Chemical Society of Japan;2013-11-15

4. Chemistry of Anthracene–Acetylene Oligomers. XXI. Structures and Stereochemistry of Chiral Anthracene–Acetylene Dimers with an Intra-Annular Alkoxy Group;Bulletin of the Chemical Society of Japan;2013-01-15

5. Host-Guest Interactions of Phosphorescent Molecular Tweezers Based on an Alkynylplatinum(II) Terpyridine System with Polyaromatic Hydrocarbons;Chemistry - A European Journal;2012-11-23