Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 32, Pages 4832-4834Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b910894g
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Funding
- EPSRC
- AZ
- EPSRC [EP/D075335/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/D075335/1] Funding Source: researchfish
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Despite their intrinsic instability, 4a-alkyl-4aH-carbazoles can be generated by a catalytic dearomatisation process; their reactivity is demonstrated by facile dealkylation and highly unusual cyclodimerisation processes.
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