Intramolecular Nitrofuran Diels–Alder Reactions: Extremely Substituent-Tolerant Cycloadditions via Asynchronous Transition States
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Halogenation effects in intramolecular furan Diels-Alder reactions: broad scope synthetic and computational studiesElectronic supplementary information (ESI) available: Experimental procedures, characterisation data, 1H and 13C NMR spectra for all new compounds; further computational experiments on model systems and full discussion of the CBS methodologies used, results for reactions of 1a-z at 298 K, dipolar interaction, selected FMO and transition state structural data. See DOI: 10.1039/c3ob41
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