18 reactions;26 products. Formula and source issues:
7b1 C26H29ClN2O2 9 []
7b2 C26H29ClN2O2 4 []
7b3 C30H35ClN2O2 4 ['Reported mass/yield arithmetic differs: 3.8mg and0.15mmol imply about5.16% for drawn MW, versus reported4%; preserve both without recalculating reported yield.']
7t1 C30H31ClN2O3 10 []
7t2 C30H31ClN2O3 9 []
7e1 C28H33ClN2O2 11 []
7e2 C28H33ClN2O2 5 ['Reported mass/yield arithmetic differs: 5.4mg and0.15mmol imply about7.74% for drawn MW, versus reported5%; preserve both without recalculating reported yield.']
7j1 C28H31ClF2N2O2 8 ['Reported mass/yield arithmetic differs: 7.8mg and0.15mmol imply about10.38% for drawn MW, versus reported8%; preserve both without recalculating reported yield.']
7j2 C28H31ClF2N2O2 6 ['Reported mass/yield arithmetic differs: 6.0mg and0.15mmol imply about7.98% for drawn MW, versus reported6%; preserve both without recalculating reported yield.']
7s C27H31ClN2O3 10 []
8s C20H22N4O2 20 []
7q1 C31H38ClN3O4 4 []
7q2 C31H38ClN3O4 4 []
28h C22H24N2O 28 []
38e C26H27BrN4OS 36 ['Source FigureS20 draws an S-cyclohexyl reduced triazoline with N-H and saturated C-H; heading names an aromatic triazole. Drawn graph has C26H27BrN4OS and calculated[M+H]+523.11617; named aromatic alternative C26H25BrN4OS has521.10052. Reported calc523.1089/found523.09 are closer to drawn saturation but not accurate exact masses. Source formula C22H24N2O is a copy-paste error. Use explicit drawing graph, mark structural inconsistency; do not silently aromatize.']
40h C17H15Cl2N3O2 52 []
33h C23H24Cl2N2O2S 44 []
37b1 C23H18ClF3N2OS 10 []
37b2 C23H18ClF3N2OS 7 []
29b C23H18ClF3N2O2 22 []
34b1 C24H24N2O3S 15 []
34b2 C24H24N2O3S 4 []
39u C23H23N3OS 3 []
35m C25H17Cl2F3N2O3 3 []
41e C22H21NO2 3 []
26e C22H21Cl2NO 22 []
