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- W1571303419 endingPage "220" @default.
- W1571303419 startingPage "183" @default.
- W1571303419 abstract "This chapter presents a progress report and retrospective on the efforts of researchers toward the synthesis of stereoregular oligocycloalkanes and ter-cyclopentane. The interest in oligocycloalkane structures has been ignited by the publication of two natural products with a stereoregular series of cyclopropane rings. The researchers have been intrigued by the challenge these molecules represent; even more so by the unique conformational properties that such molecules are likely to have. This has applied for a host of other cycloalkane oligomers also. Contention that well-substituted oligocyclopentanes might be receptors for a variety of target molecules is based on extensive molecular mechanics simulations, which suggests that such structures would be conformationally rigid and able to present functionality in a spatially defined manner. In a simple, qualitative analysis, it is expected that in the lowest energy conformer for a dicyclopentane, the torsional angle connecting the two rings should be approximately 180°(or “anti”) because this minimizes the number of gauche butane interactions. A similar qualitative analysis of ter-cyclopentane would predict that its ground-state conformation would be that in which both inter-ring torsional angles are at 180°." @default.
- W1571303419 created "2016-06-24" @default.
- W1571303419 creator A5051981217 @default.
- W1571303419 creator A5063136685 @default.
- W1571303419 date "2004-01-01" @default.
- W1571303419 modified "2023-09-25" @default.
- W1571303419 title "Chapter 7 Development of general synthetic strategies towards oligocycloalkanes" @default.
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