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• W4303856998 endingPage "M1457" @default.
• W4303856998 startingPage "M1457" @default.
• W4303856998 abstract "Enantiomers (2S, 4S)- and (2R, 4R)-3-(naphthalene-1-ylmethyl) pentane-2,4-diols were synthesized by the reduction of (Z)-4-hydroxy-3-(naphthalene-1-ylmethyl) pent-3-en-2-one with NaBH4 in methanol (MeOH). Crystallization in dichloromethane of this racemic mixture led to simple crystals with a crystalline habit with similar morphologies; however, in a group of them, it was possible to find a barely observable difference that allowed determining a crystal structure for each of the enantiomers, the 2S,4S, and the 2R,4R." @default.
• W4303856998 created "2022-10-09" @default.
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• W4303856998 date "2022-09-30" @default.
• W4303856998 modified "2023-10-17" @default.
• W4303856998 title "Spontaneous Enantiomeric Resolution of 1,3-Diols from the Naphtylidene Derivative of 2,4-Pentanedione" @default.
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• W4303856998 doi "https://doi.org/10.3390/m1457" @default.
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