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Synthesis of Asymmetric Septi(p-Phenylene)s |
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Published in | Tetrahedron letters. 1998, vol. 39, no. 30, p. 5335-5338 | |
Abstract | In this Letter, we describe the synthesis of two amphiphilic septi(p-phenylene)s. One terminus of each rigid-rod scaffold is linked through a spacer to a hydrophilic IDA-subunit, the two benzenes at the other terminus carry hydrophobic substituents of different size. These synthetic receptor models are expected to mimic biological processes that occur at cell membranes. | |
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Citation (ISO format) | GHEBREMARIAM, Bereket, MATILE, Stefan. Synthesis of Asymmetric Septi(p-Phenylene)s. In: Tetrahedron letters, 1998, vol. 39, n° 30, p. 5335-5338. doi: 10.1016/S0040-4039(98)01041-7 https://archive-ouverte.unige.ch/unige:7002 |