Volume 21, Issue 37
Preparative Organic Chemistry
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ChemInform Abstract: Intramolecular (2 + 2)Photocycloaddition. Part 7. Efficient Intramolecular (2 + 2)Photocycloaddition of Styrene Derivatives Toward New Crown Ethers.

S. INOKUMA

S. INOKUMA

Dep. Chem., Fac. Eng., Gunma Univ., Kiryu, Gunma 376, Japan

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T. YAMAMOTO

T. YAMAMOTO

Dep. Chem., Fac. Eng., Gunma Univ., Kiryu, Gunma 376, Japan

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J. NISHIMURA

J. NISHIMURA

Dep. Chem., Fac. Eng., Gunma Univ., Kiryu, Gunma 376, Japan

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First published: September 11, 1990

Abstract

4-Hydroxyacetophenone (I) is coupled with oligoethylene glycol bistosylates (II) to form the bridged bisacetophenones (III).

ChemInform Abstract

4-Hydroxyacetophenone (I) is coupled with oligoethylene glycol bistosylates (II) to form the bridged bisacetophenones (III). These are converted to the bisvinyl compounds (IV) which cyclize under irradiation to give the macrocycles (V) and (VI). Further examples with different reaction conditions are given in the original paper. The compounds show high selectivity for lithium cations in solid-liquid extraction.

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