Volume 29, Issue 1
Isocyclic Compounds
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ChemInform Abstract: 2-Functionalized Furans as Precursors of Versatile Cycloheptane Synthons.

A. M. MONTANA

A. M. MONTANA

Dep. Quim. Org., Fac. Quim., Univ. Barcelona, E-08028 Barcelona, Spain

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S. RIBES

S. RIBES

Dep. Quim. Org., Fac. Quim., Univ. Barcelona, E-08028 Barcelona, Spain

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P. M. GRIMA

P. M. GRIMA

Dep. Quim. Org., Fac. Quim., Univ. Barcelona, E-08028 Barcelona, Spain

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F. GARCIA

F. GARCIA

Dep. Quim. Org., Fac. Quim., Univ. Barcelona, E-08028 Barcelona, Spain

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X. SOLANS

X. SOLANS

Dep. Quim. Org., Fac. Quim., Univ. Barcelona, E-08028 Barcelona, Spain

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M. FONT-BARDIA

M. FONT-BARDIA

Dep. Quim. Org., Fac. Quim., Univ. Barcelona, E-08028 Barcelona, Spain

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First published: 24 June 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The outcome of the [4 + 3]cycloaddition, which in most cases proceeds with cis-diastereospecificity and high endo selectivity, is found to depend on steric and electronic effects. Increasing bulkiness of the 2-substituents results in increase of endo selectivity, but decrease of yield. Increasing electronic density of the furan system by electron donating groups at C-2 leads to better yields and diastereoselectivities.

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