A NOVEL REACTION OF 8,16-BIS(BROMOMETHYL) [2.2]METACYCLOPHANES WITH PHENYL LITHIUM AND PREPARATION OF 8,16-UNSYMMETRICALLY DISUBSTITUTED [2.2]METACYCLOPHANES-Reference-Cited by-同舟云学术

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A NOVEL REACTION OF 8,16-BIS(BROMOMETHYL) [2.2]METACYCLOPHANES WITH PHENYL LITHIUM AND PREPARATION OF 8,16-UNSYMMETRICALLY DISUBSTITUTED [2.2]METACYCLOPHANES

Published:1982-01-05 Issue:1 Volume:11 Page:61-64
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Tashiro Masashi,Yamato Takehiko

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference2 articles.

1. Selective preparation. 30. A convenient preparation of 5,13-di-tert-butyl-8,16-disubstituted-[2.2]metacyclophanes and their trans-tert-butylation and halogenation reactions

2. The Chemistry of Xylylenes. VIII. The Formation of Spiro-di-o-xylylene and Related Compounds1

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1. Regioselective activation of benzocyclobutenones and dienamides lead to anti-Bredt bridged-ring systems by a [4+4] cycloaddition;Nature Communications;2021-05-21

2. Medium-sized cyclophanes — Part 85: Benzylation by 8-(bromomethyl)[2.2]metacyclophanes. Through-space electronic interactions of [2.2]metacyclophane benzyl cations;Canadian Journal of Chemistry;2010-05

3. Phenyllithium;Encyclopedia of Reagents for Organic Synthesis;2008-03-14

4. An Acid Catalysed Intramolecular C–C Coupling Reaction of 8-halomethyl-16-methoxy[2.2]Metacyclophanes;Journal of Chemical Research;2005-08

5. Phenyllithium;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

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