Under optimal conditions the reactions exhibit high para selectivity with little or no adamantane sideproduct being formed: Revision history

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25 March 2024

  • curprev 04:2404:24, 25 March 2024‎ Copyplane5 talk contribs‎ 5,464 bytes +5,464‎ Created page with "The synthetic scope of this transformation was tested for representative alkylbenzenes and haloalkylbenzenes. [https://sensible-carnation-h1pfjj.mystrikingly.com/blog/monitoring-snps-is-of-significant-benefit-to-drug-design-and-disease-diagnosis 6-butyl-n-hydroxynaphthimide trifluoromethanesulfonic acid in Medicinal Chemistry] carried out in 1,2-dichloroethane (DCE) produce increased amounts of the meta isomer and substantial amounts of adamantane. Substrate selectivitie..."
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