2005
DOI: 10.1070/mc2005v015n04abeh002136
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Chirality-directed organogel formation

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Cited by 32 publications
(6 citation statements)
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“…Pure R-enantiomer of the seventh member of the homologous series of trifluoroacetylated α-amino alcohols (TFAAA-7R, Figure 1) was synthesized according to the procedure described earlier. 22 Glycerol (Khimmed, Russia) was heated to a temperature of 60-70 ∘ C and mixed with TFAAA-7R powder under stirring (final concentration 10 mg/mL). After the dissolution of TFAAA, 15μL of the hot solution was dropped onto the surface of the glass slide and covered with a coverslip (the gap was $ 0:5 mm).…”
Section: Methodsmentioning
confidence: 99%
“…Pure R-enantiomer of the seventh member of the homologous series of trifluoroacetylated α-amino alcohols (TFAAA-7R, Figure 1) was synthesized according to the procedure described earlier. 22 Glycerol (Khimmed, Russia) was heated to a temperature of 60-70 ∘ C and mixed with TFAAA-7R powder under stirring (final concentration 10 mg/mL). After the dissolution of TFAAA, 15μL of the hot solution was dropped onto the surface of the glass slide and covered with a coverslip (the gap was $ 0:5 mm).…”
Section: Methodsmentioning
confidence: 99%
“…Pure R-enantiomer of seventh member of the homologous series of trifluoroacetylated α-aminoalcohols (TFAAA-7R, Fig. 2) was synthesized according to the procedure described earlier 28 . Glycerol (Khimmed, Russia) was heated to a temperature 4/7 of 60-70 • C and mixed with TFAAA-7R powder under stirring (final concentration 10 mg/ml).…”
Section: Methodsmentioning
confidence: 99%
“…TFAAA molecules were synthesized as described earlier. 14,29 Solutes were purchased from Chimmed (Moscow, Russia).…”
Section: Methodsmentioning
confidence: 99%