Absolute Conformation and Chiroptical Properties. VI. 2,2′,3,3′-Tetramethoxy-9,9′-bitriptycyl: A Stereochemical Analog of 1,2-Disubstituted Ethane with Identical Substituents-Reference-Cited by-同舟云学术

Absolute Conformation and Chiroptical Properties. VI. 2,2′,3,3′-Tetramethoxy-9,9′-bitriptycyl: A Stereochemical Analog of 1,2-Disubstituted Ethane with Identical Substituents

Published:1998-11 Issue:11 Volume:71 Page:2715-2720
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Toyota Shinji,Yasutomi Akihiro,Kojima Hiroharu,Igarashi Yuko,Asakura Mitsuhiro,Oki Michinori

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/71/11/71_11_2715/_pdf

Reference23 articles.

1. Syntheses of ap- and ±sc-2,2′,3,3′-tetramethoxy-9,9′-bitriptycyl rotamers and optical resolution of the ±sc-form

2. Absolute Stereochemistry of Dimethyl 9-(1,1-Dimethyl-2-phenylethyl)-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboxylate Rotamers.

3. Absolute Conformation and Chiroptical Properties. III. Optically Active Methylsc-3-Methyl-3-(substituted 9-triptycyl)butanoate Rotamers

4. Absolute Conformation and Substituent Effects on Chiroptical Properties of 9-(2-Halo-1,1-dimethylethyl)-11,12- bis(methoxycarbonyl)-9,10-dihydro-9,10-ethenoanthracenes1,2

5. The first synthesis and resolution of some chiral carbon compounds having four different labile ligands

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