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“…Selected tri‐, tetra‐, and pentacycle‐based melatonin receptor ligands. 29 : Epperson et al 108 ; 30: Landagaray et al 105 ; 31 : Lucini et al 55 ; 32 : Tsotinis et al 58 ; 33 : Bedini et al 46 ; 34 : Jellimann et al 47 ; 35 : Uchikawa et al 72 ; 36 : Tsotinis et al 65 ; 37 : Koike et al 90 ; 38, 39 & 40 : Davies et al 122 ; 41 : Spadoni et al 87 ; 42 : Landagaray et al 85 ; 43 : Kobayashi et al 33 ; 44 : Attia et al 29 ; 45 : Faust et al 113 …”
Section: The Pharmacophores (The Others Figure 5: Tri‐ and Tetra‐cycles)unclassified
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“…Selected tri‐, tetra‐, and pentacycle‐based melatonin receptor ligands. 29 : Epperson et al 108 ; 30: Landagaray et al 105 ; 31 : Lucini et al 55 ; 32 : Tsotinis et al 58 ; 33 : Bedini et al 46 ; 34 : Jellimann et al 47 ; 35 : Uchikawa et al 72 ; 36 : Tsotinis et al 65 ; 37 : Koike et al 90 ; 38, 39 & 40 : Davies et al 122 ; 41 : Spadoni et al 87 ; 42 : Landagaray et al 85 ; 43 : Kobayashi et al 33 ; 44 : Attia et al 29 ; 45 : Faust et al 113 …”
Section: The Pharmacophores (The Others Figure 5: Tri‐ and Tetra‐cycles)unclassified
“…In 2005, Spadoni and co-workers 18 employed the same strategy for the synthesis of Uhle's ketone derivative 35. In this case, the intramolecular Friedel-Crafts cyclization was followed by esterification with diazomethane.…”
Section: Disconnection B: Intramolecular Friedel-crafts Cyclizationmentioning
“…Scheme 5 1964 Szmuszkovicz17 and 2005 Spadoni and co-workers18 synthesis of Uhle's ketones 33-35 from indolylsuccinic anhydride derivatives…”
mentioning
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