1983
DOI: 10.1039/p19830000413
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Scensidin, a new depsidone from the lichen Buellia canescens(Dicks.) De Not

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Cited by 8 publications
(2 citation statements)
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“…yellow powder (CH 2 Cl 2 ); UV (MeOH) λ max (log ε) 231 (4.60), 263 (4.10), 285 (3.94) nm; 1 H NMR (CDCl 3 , 500 MHz) data comparable to published data; 13 C NMR (CDCl 3 , 125 MHz) δ 162.3 (COO, C-7), 161.3 (C, C-2), 158.7 (C, C-4), 152.7 (C, C-2′), 142.9 (C, C-4′, C-5′), 142.1 (C, C-6), 130.3 (C, C-6′), 121.5 (C, C-5), 119.3 (C, C-1′), 114.9 (C, C-1), 101.9 (C, C-3′), 101.3 (CH, C-3), 56.6 (OCH 3 , C-8), 56.5 (OCH 3 , C-8′), 18.5 (CH 3 , C-9), 13.8 (CH 3 , C-7′); EIMS m / z 368 [M] + , 333 [M − Cl] + , 318 [M − CH 3 − Cl] + , 305 [M − CO − Cl] + ; HREIMS m / z 368.0217 [M] + (calcd for C 17 H 14 O 5 Cl 2 368.0218); R f 0.69 (toluene−EtOAc−formic acid, 7:2:0.5).…”
Section: Methodssupporting
confidence: 57%
“…yellow powder (CH 2 Cl 2 ); UV (MeOH) λ max (log ε) 231 (4.60), 263 (4.10), 285 (3.94) nm; 1 H NMR (CDCl 3 , 500 MHz) data comparable to published data; 13 C NMR (CDCl 3 , 125 MHz) δ 162.3 (COO, C-7), 161.3 (C, C-2), 158.7 (C, C-4), 152.7 (C, C-2′), 142.9 (C, C-4′, C-5′), 142.1 (C, C-6), 130.3 (C, C-6′), 121.5 (C, C-5), 119.3 (C, C-1′), 114.9 (C, C-1), 101.9 (C, C-3′), 101.3 (CH, C-3), 56.6 (OCH 3 , C-8), 56.5 (OCH 3 , C-8′), 18.5 (CH 3 , C-9), 13.8 (CH 3 , C-7′); EIMS m / z 368 [M] + , 333 [M − Cl] + , 318 [M − CH 3 − Cl] + , 305 [M − CO − Cl] + ; HREIMS m / z 368.0217 [M] + (calcd for C 17 H 14 O 5 Cl 2 368.0218); R f 0.69 (toluene−EtOAc−formic acid, 7:2:0.5).…”
Section: Methodssupporting
confidence: 57%
“…The organic layer was washed with water, dried, and evaporated to dryness. The residual solid was crystallised from methanol to give the depsidone (2)…”
Section: -Bromo-3-hydroxy-8-rnethoxy-l69-triinethyl-l1 H-dibenzu-[be]...mentioning
confidence: 99%