MOF confinement enables selective synthesis of novel oxazoles from indole and formaldehyde
Herein, we report the successful guidance of indole and formaldehyde reactivity by precisely tuning the pore size and active sites of MOF, altering their intrinsic reaction pathways. This led to the first example of novel compounds synthesized through the synergistic catalysis enabled by MOF confine...
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Published in | Chemical communications (Cambridge, England) Vol. 61; no. 12; pp. 252 - 2523 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
CAMBRIDGE
Royal Soc Chemistry
04.02.2025
Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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Summary: | Herein, we report the successful guidance of indole and formaldehyde reactivity by precisely tuning the pore size and active sites of MOF, altering their intrinsic reaction pathways. This led to the first example of novel compounds synthesized through the synergistic catalysis enabled by MOF confinement. Detailed mechanistic studies revealed that the confined environment within the MOF pores promoted the occurrence of multi-stage cascade reactions and stabilized specific reaction pathways.
The high reactivity of indole and formaldehyde has been successfully controlled through the confinement effect of MOF, enabling the highly selective synthesis of novel oxazole compounds
via
a specific reaction pathway. |
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Bibliography: | https://doi.org/10.1039/d4cc06486k Electronic supplementary information (ESI) available. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1359-7345 1364-548X 1364-548X |
DOI: | 10.1039/d4cc06486k |