Chlorodecarboxylation of 3-Methyl-3-(1,4-dimethyl-9-triptycyl)butanoic Acid Rotamers with Lead(IV) Acetate in the Presence of Lithium Chloride. Facile Hydrogen Transfer from the 1-Methyl Group in the sc-Isomer-Reference-Cited by-同舟云学术

Chlorodecarboxylation of 3-Methyl-3-(1,4-dimethyl-9-triptycyl)butanoic Acid Rotamers with Lead(IV) Acetate in the Presence of Lithium Chloride. Facile Hydrogen Transfer from the 1-Methyl Group in the sc-Isomer

Published:1990-02 Issue:2 Volume:19 Page:199-202
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Oki Michinori,Okamoto Toshiyuki,Toyota Shinji,Yonemoto Katsumi,Yamamoto Gaku

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/19/2/19_2_199/_pdf

Reference13 articles.

1. Reactivity of conformational isomers

2. Reactivities of Stable Rotamers. XXII. Lewis Acid-Catalyzed Reactions of 3-(1,4-Disubstituted 9-Triptycyl)-3-methylbutanoyl Chloride: Isolation of Rotameric Ketones and Competition between Cyclizations to Substituted and to Unsubstituted Benzene Rings

3. Formation of Alkyl Halides from Acids by Decarboxylation with Lead(IV) Acetate and Halide Salts

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1. Reactivities of Stable Rotamers. XXXV. Diazotization of 2-(1,4-Dimethyl-9-triptycyl)-2-methylpropylamine Rotamers;Bulletin of the Chemical Society of Japan;1995-05

2. Substantial differences in the product distributions between thermolyses and photolyses of 2-thiono-1-pyridyl 3-(1,4-dimethyl-9-triptycyl)-3-butanoate ester and the effects of rotational isomerism;Tetrahedron Letters;1995-02

3. Reactivities of Stable Rotamers. XXXII. Chlorodecarboxylation of 3-(1,4-Dimethyl-9-triptycyl)-3-methylbutanoic Acid Rotamers;Bulletin of the Chemical Society of Japan;1993-12

4. Syntheses and Structures of 1,1-Dimethyl-1,2,6,10b-tetrahydro-6,10b-o-benzenoaceanthrylenes: Sterically Congested Triptycenes Carrying Five-Membered Ring;Bulletin of the Chemical Society of Japan;1993-07

5. How Do Ethane-Type Molecules Avoid Eclipsing When Forced as Such? The Case of 7,8,9,10-Tetrachloro-1,1-dimethyl-1,2,6,10b-tetrahydro-6,10b-o-benzenoaceanthrylene;Chemistry Letters;1992-02