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Self-replication vs. reactive binary complexes--manipulating recognition-mediated cycloadditions by simple structural modifications
The rate of reaction and the selectivity of a Diels-Alder cycloaddition between a furan and a maleimide can be enhanced by the introduction of complementary recognition sites on the reactant species. Subtle manipulation of other structural elements allows the generation of the observed rate enhancem...
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Published in: | Organic & biomolecular chemistry 2004-12, Vol.2 (23), p.3434-3441 |
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Language: | English |
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container_end_page | 3441 |
container_issue | 23 |
container_start_page | 3434 |
container_title | Organic & biomolecular chemistry |
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creator | Pearson, Russell J Kassianidis, Eleftherios Slawin, Alexandra M Z Philp, Douglas |
description | The rate of reaction and the selectivity of a Diels-Alder cycloaddition between a furan and a maleimide can be enhanced by the introduction of complementary recognition sites on the reactant species. Subtle manipulation of other structural elements allows the generation of the observed rate enhancements and selectivities through either self-replication or formation of a pre-reactive binary complex. |
doi_str_mv | 10.1039/b406862a |
format | article |
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source | Royal Society of Chemistry: Jisc Collections: Journals Archive 1841-2007 (2019-2023) |
title | Self-replication vs. reactive binary complexes--manipulating recognition-mediated cycloadditions by simple structural modifications |
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