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Conditions | Yield |
---|---|
With sodium periodate; ruthenium trichloride In water; acetonitrile at 20℃; for 2h; | 47% |
With sodium periodate; ruthenium dioxide dihydrate In tetrachloromethane; water; acetonitrile at 20℃; for 2.83333h; Inert atmosphere; | Ca. 3.00 g |
Conditions | Yield |
---|---|
With hypochloric acid Behandeln des Reaktionsprodukts mit alkoh. Kali; | |
With perchloric acid; acetic acid; quinolinium chlorochromate(VI) at 39.85℃; Kinetics; Further Variations:; Temperatures; | |
With perchloric acid; dihydrogen peroxide In water; acetonitrile; tert-butyl alcohol at 59.84℃; under 760.051 Torr; for 1h; Inert atmosphere; | 56 %Chromat. |
With perchloric acid; tetraethylammonium chlorochromate(VI); sodium perchlorate; acetic acid In water at 29.84℃; for 24h; Kinetics; Concentration; Temperature; | |
With 7H2O*3H3N*3H(1+)*[FeMo6O18(OH)6](3-); dihydrogen peroxide; sodium hydrogencarbonate In acetonitrile at 50℃; for 10h; chemoselective reaction; | 95 %Chromat. |
Conditions | Yield |
---|---|
With -base Kinetik; dl-glycidic acid; | |
With potassium hydroxide dl-glycidic acid; |
acide 2-bromo-3-hydroxy propanoique
glycidic acid
Conditions | Yield |
---|---|
With potassium hydroxide; nitric acid 1.) methanol, -40 deg C --> 0 deg C; 2.) water, -5 deg C, 1 h; Yield given; |
Conditions | Yield |
---|---|
With Oxone In water-d2 for 0.25h; Product distribution; Ambient temperature; pH 6.8 (phosphate buffer); |
Conditions | Yield |
---|---|
With Acetobacter pasteurianus LMG 1635 In water at 30℃; Kinetics; |
glycidic acid
Conditions | Yield |
---|---|
With sodium ethanolate |
2-chloro-3-hydroxypropionic acid
glycidic acid
Conditions | Yield |
---|---|
at 20℃; |
D-(+)-camphoric acid
water
A
formic acid
B
oxalic acid
C
acetic acid
D
glycidic acid
D-(+)-camphoric acid
water
A
2,3,3-trimethylsuccinic acid
B
oxalic acid
C
glycidic acid
D
butyric acid
D-(+)-camphoric acid
water
A
(+-)-camphoronic acid
B
oxalic acid
C
glycidic acid
2-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)ethan-1-amine
glycidic acid
N-[O,O'-di-(tert-butyl-dimethylsilyl)dopaminyl]-glycidamide
Conditions | Yield |
---|---|
Stage #1: glycidic acid With 4-methyl-morpholine; isobutyl chloroformate In dichloromethane at 0℃; for 1h; Cooling with ice; Inert atmosphere; Stage #2: 2-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)ethan-1-amine With 4-methyl-morpholine In dichloromethane at 0℃; Inert atmosphere; | 56% |
Conditions | Yield |
---|---|
With ammonium peroxydisulfate; anthocyanin In dichloromethane; water at 20℃; Minisci Aromatic Substitution; Irradiation; Green chemistry; | 55% |
Conditions | Yield |
---|---|
Stage #1: glycidic acid With 4-methyl-morpholine; isobutyl chloroformate In dichloromethane at 0℃; for 1h; Cooling with ice; Inert atmosphere; Stage #2: 1-Adamantanamine With 4-methyl-morpholine In dichloromethane at 0℃; Inert atmosphere; | 52% |
oxalyl dichloride
N-{5-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide hydrochloride
glycidic acid
1,3-dimethyl-N-[2-methyl-5-({2-[(oxirane-2-ylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)phenyl]-1H-pyrazole-5-carboxamide
Conditions | Yield |
---|---|
In tetrahydrofuran; N,N-dimethyl acetamide; N,N-dimethyl-formamide | 52% |
glycidic acid
Conditions | Yield |
---|---|
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 1h; | 40% |
glycidic acid
Conditions | Yield |
---|---|
Stage #1: glycidic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 0.5h; Inert atmosphere; Stage #2: N-((3R,6S)-6-methylpiperidin-3-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 1h; | 23% |
glycidic acid
Conditions | Yield |
---|---|
Stage #1: trans-N-(4-aminocyclohexyl)-2-(4-chloro-3-fluorophenoxy)acetamide With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: glycidic acid In N,N-dimethyl-formamide at 20℃; | 20% |
7-chloro-1H-indole
glycidic acid
3-(7-chloro-1H-indol-3-yl)-2-hydroxy-propionic acid
Conditions | Yield |
---|---|
With tin(IV) chloride In tetrachloromethane at 0℃; for 1.5h; | 7% |
glycidic acid
Conditions | Yield |
---|---|
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 25℃; for 24h; | 3.1% |
glycidic acid
2-hydroxy-3-iodo-propionic acid
Conditions | Yield |
---|---|
With hydrogen iodide |
Conditions | Yield |
---|---|
With ammonia; water at 120℃; inactive α-oxy-β-amino-propionic acid; | |
With ethanol; ammonia inactive α-oxy-β-amino-propionic acid; |
Conditions | Yield |
---|---|
With water |
glycidic acid
(R,S)-3-bromo-2-hydroxypropanoic acid
Conditions | Yield |
---|---|
With hydrogen bromide |
Conditions | Yield |
---|---|
With hydrogen bromide at 140℃; | |
With phosphorus halides nachfolgende Behandlung mit Wasser; | |
at 170 - 220℃; das Anhydrid entsteht; |
glycidic acid
erythro-9,10-dihydroxystearic acid
Conditions | Yield |
---|---|
With sulfuric acid | |
With potassium hydroxide |
Conditions | Yield |
---|---|
With hydrogenchloride |
dimethyl amine
glycidic acid
A
3-dimethylamino-2-hydroxy-propionic acid
B
N,N-dimethylserine
Conditions | Yield |
---|---|
In diethyl ether; water for 2h; Product distribution; Ambient temperature; |
Conditions | Yield |
---|---|
In diethyl ether; water for 3h; Product distribution; Ambient temperature; |
Conditions | Yield |
---|---|
With ammonia In diethyl ether; water for 6h; Product distribution; Ambient temperature; |
Conditions | Yield |
---|---|
at 120℃; im Einschlussrohr; |
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