“Living” Nature in Anionic Cyclopolymerization of 1,2:5,6-Dianhydro-3,4-di-O-methyl-d-mannitol Using the Potassium tert-Butoxide/18-Crown-6 Initiating System-Reference-Cited by-同舟云学术

“Living” Nature in Anionic Cyclopolymerization of 1,2:5,6-Dianhydro-3,4-di-O-methyl-d-mannitol Using the Potassium tert-Butoxide/18-Crown-6 Initiating System

Published:1998-04-17 Issue:9 Volume:31 Page:2889-2893
ISSN:0024-9297
Container-title:Macromolecules
language:en
Short-container-title:Macromolecules

Author:

Hatakeyama Takeshi¹,Kamada Masatoshi¹,Satoh Toshifumi¹,Yokota Kazuaki¹,Kakuchi Toyoji²

Affiliation:

1. Division of Molecular Chemistry, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628, Japan

2. Division of Bioscience, Graduate School of Environmental Earth Science, Hokkaido University, Sapporo 060-0810, Japan

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Inorganic Chemistry,Polymers and Plastics,Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ma9709765

Reference26 articles.

1. Activation of 6-endo over 5-exo epoxide openings. Ring-selective formation of tetrahydropyran systems and stereocontrolled synthesis of the ABC ring framework of brevetoxin B

2. Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systems

3. Activation of 7-endo over 6-exo epoxide openings. Synthesis of oxepane and tetrahydropyran systems

4. Ring size in epoxynitrile cyclization. General synthesis of functionally substituted cyclobutanes. Application to (+-)-grandisol

5. 3,4-di-O-alkyl-1,6-dibromo-1,6-dideoxyhexitols

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