Inclusion Properties of Acyclic Phenol–Formaldehyde Oligomer Analogs Containing 2,2′-Dihydroxybiphenyl or 2,2′-Dihydroxy-1,1′-binaphthyl Unit
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/67/12/67_12_3366/_pdf
Reference14 articles.
1. Inclusion Properties of Acyclicp-Substituted Phenol–Formaldehyde Oligomers
2. Synthesis and Inclusion Properties of Sulfur-Bridged Analogs of Acyclic Phenol-Formaldehyde Oligomers
3. Synthesis and Inclusion Properties of Carbonyl-Bridged Analogs of Acyclicp-t-Butylphenol–Formaldehyde Oligomers
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1. Binol Quinone Methides as Bisalkylating and DNA Cross-Linking Agents;Journal of the American Chemical Society;2004-10-09
2. FACILE PREPARATION OF O-SUBSTITUTED ACYCLIC PHENOL–FORMALDEHYDE OLIGOMERS;Synthetic Communications;2002-01-01
3. Synthesis and Properties of Calixarene Analogs Modified in the Macrocyclic Ring.;NIPPON KAGAKU KAISHI;1999
4. Synthesis and properties of sulfur-bridged analogs of p-tert-Butylcalix[4]arene;Tetrahedron;1997-08
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