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Beilstein J. Org. Chem. 2020, 16, 809–817, doi:10.3762/bjoc.16.74
Graphical Abstract
Scheme 1: Examples of photocatalytic C–C bond formation by nucleophilic trapping of a reactive THIQ intermedi...
Figure 1: Kinetic profile for the benzylation of 1 to 3.
Scheme 2: Benzylation of N-phenyl-THIQ.
Scheme 3: Benzylation of substituted N-arylTHIQs.
Scheme 4: Removal of the PMP protecting group.
Scheme 5: Alkylation of N-phenyl-THIQ derivatives. Conditions: a2 mol % [Ir(dtbbpy)(ppy)2]PF6, DMA, 60 h; b2 ...
Scheme 6: Proposed mechanism.
Beilstein J. Org. Chem. 2014, 10, 2186–2199, doi:10.3762/bjoc.10.226
Figure 1: General structures of biologically active dihydroisoquinolines, THIQs and 1,2-diarylindoles.
Scheme 1: Li’s THIQ indolation protocol.
Scheme 2: Possible strategies for the synthesis of target structure 1. Dashed arrows indicate literature-know...
Scheme 3: Nucleophilic substitution of DMEDA with 2-fluoro-3-iodopyridine (10).
Scheme 4: Decomposition of 1-(indol-3-yl)-THIQ 4d during N-arylation (monitored by GC–MS).
Scheme 5: Formation of byproduct 13 via benzylic oxidation.
Scheme 6: Routes towards 1,2-diarylindoles starting from indole; a: PhB(OH)2 (3 equiv), Pd(OAc)2 (5 mol %), A...
Scheme 7: Palladium-catalyzed C2-arylation attempt of 1-(1-phenylindol-3-yl)-N-Boc-THIQ.