An efficient synthetic entry to rotaxanes utilising reversible cleavage of aromatic disulphide bonds-Reference-Cited by-同舟云学术

An efficient synthetic entry to rotaxanes utilising reversible cleavage of aromatic disulphide bonds

Published:2010-08-31 Issue:1-2 Volume:23 Page:65-68
ISSN:1061-0278
Container-title:Supramolecular Chemistry
language:en
Short-container-title:Supramolecular Chemistry

Author:

Yoshii Takahiro¹,Kohsaka Yasuhiro¹,Moriyama Taichi¹,Suzuki Takao¹,Koyama Yasuhito¹,Takata Toshikazu¹

Affiliation:

1. a Department of Organic and Polymeric Materials , Tokyo Institute of Technology , 2-12-1 H-126, O-okayama, Meguro-ku, Tokyo, 152-8552, Japan

Publisher

Informa UK Limited

Subject

General Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10610278.2010.510192

Reference12 articles.

1. Relatively high-yield syntheses of rotaxanes. Syntheses and properties of compounds consisting of cyclodextrins threaded by .alpha.,.omega.-diaminoalkanes coordinated to cobalt(III) complexes

2. For reviews, see: (a) Takata , T. 2009. Bottom-Up Nanofabrication: Supramolecules, Self-Assemblies, and Organized Films, chapter 2 Edited by: Ariga , K. and Nalwa , H.S. 311–329. Los Angels, CA: American Scientific Publishers. (b) Fyfe, M.C.T.; Stoddart, J.F.; Williams, D.J.Struct. Chem.1999,10, 243–259

3. Synthesizing interlocked molecules dynamically

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