Remarkable Effects of Chirality on Deslipping Reactions of Diastereomeric Rotaxanes and Relevant Mechanism Involving Pre-Equilibrium
Author:
Affiliation:
1. Division of Frontier Materials Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka 563-8531, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol802571d
Reference17 articles.
1. The Mechanism of the Slippage Approach to Rotaxanes. Origin of the “All-or-Nothing” Substituent Effect
2. Rotaxane or Pseudorotaxane? That Is the Question!
3. A Rotaxane-Like Complex with Controlled-Release Characteristics
4. The Spatial Demand of Dendrimers: Deslipping of Rotaxanes
5. Rotaxane or Pseudorotaxane? Effects of Small Structural Variations on the Deslipping Kinetics of Rotaxanes with Stopper Groups of Intermediate Size
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2. Ring‐to‐Thread Chirality Transfer in [2]Rotaxanes for the Synthesis of Enantioenriched Lactams;Angewandte Chemie International Edition;2022-08-19
3. Ring‐to‐Thread Chirality Transfer in [2]Rotaxanes for the Synthesis of Enantioenriched Lactams;Angewandte Chemie;2022-08-19
4. Homo and heteroassembly of amide-based [2]rotaxanes using α,α′-dimethyl-p-xylylenediamines;Chemical Communications;2019
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