Optically Active 9,10-Dihydro-9,10-etheno and -ethanoanthracenes. I. Syntheses of Optically Active 1,5-Disubstituted-9,10-dihydro-9,10-etheno and -ethanoanthracenes.-Reference-Cited by-同舟云学术

Optically Active 9,10-Dihydro-9,10-etheno and -ethanoanthracenes. I. Syntheses of Optically Active 1,5-Disubstituted-9,10-dihydro-9,10-etheno and -ethanoanthracenes.

Published:1973-03 Issue:3 Volume:46 Page:915-920
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Tatemitsu Hitoshi,Ogura Fumio,Nakagawa Masazumi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference14 articles.

1. Synthesis of Trisubstituted Triptycenes and the Optical Resolution of 7-Carboxy-2,5-diacetoxytriptycene

2. Optically Active Triptycenes. II. Synthesis of Optically Active 7-Substituted 2,5-Dimethoxytriptycenes

3. Optically Active Triptycenes, III. Synthesis of Optically Active 2-Methoxy-5-acyloxy- and 2-Acyloxy-5-methoxy-7-methoxycarbonyltriptycenes

4. Optically Active Triptycenes, V. Synthesis, Optical Resolution and Absolute Configuration of 2,7-Disubstituted Triptycenes.

5. The crystal structure and absolute configuration of (+)-2,5-dimethoxy-7-dimethylaminotriptycene hydrobromide

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1. Chiral Triptycenes in Supramolecular and Materials Chemistry;ChemistryOpen;2020-06

2. Static and dynamic stereochemistry of 1,1?-bi(9,10-dihydro-9,10-ethano-anthryl);Monatshefte f�r Chemie Chemical Monthly;1991-12

3. Synthesis and Absolute Stereochemistry of (+)-6,15-Dihydro-6,15-ethanonaphtho[2,3-c]pentaphene as Determined by Exciton Chirality and X-Ray Bijvoet Methods;Bulletin of the Chemical Society of Japan;1977-08

4. Optical Activity and Absolute Configuration of 2,3 :6,7-Dibenzobicyclo [3.3.1]nona-2,6-diene Derivatives;Bulletin of the Chemical Society of Japan;1975-09

5. ChemInform Abstract: OPTISCH AKTIVE 9,10-DIHYDRO-9,10-AETHENO- UND -AETHANO-ANTHRACENE 1. MITT. SYNTH. OPTISCH AKTIVER 1,5-DISUBSTITUIERTER 9,10-DIHYDRO-9,10-AETHENO- UND -AETHANO-ANTHRACENE;Chemischer Informationsdienst;1973-06-05