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    Supplementary Figure S1-S3. from Alterations in DNA Damage Repair Genes in Primary Liver Cancer
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    Abstract:
    <p>Supplementary Figure S1-S3.</p>
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    Primary (astronomy)
    [reaction: see text] Treatment of primary aliphatic amines with KOH in diethylene glycol at 210 degrees C gives primary alcohols directly in good yields. A synthetic application to a model study of (+/-)-scopadulin is also described.
    Primary (astronomy)
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    Primary alcohol
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    Highly selective splitting of secondary amines to primary amines with ammonia was achieved with pentaphenyl–Cp complexes of Ru, previously reported as racemization catalysts for alcohols and amines.
    Primary (astronomy)
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    Various primary alcohols, and primary, secondary, and tertiary amines were oxidatively and efficiently converted into the corresponding nitriles in good yields, by 1,3-diiodo-5,5-dimethylhydantoin (DIH) in aqueous ammonia (NH3) at 60 °C.
    Primary (astronomy)
    Tertiary alcohols
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    A general and mild method for the N-arylation of primary and secondary aliphatic amines is reported. Copper acetate, triethylamine mediated C/N cross-coupling reaction of arylboronic acids at room temperature to solid-supported primary and secondary amines gave good to excellent yields of the desired N-arylated products.
    Primary (astronomy)
    Triethylamine
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    Abstract Aus den Tetrahydro‐dibenzoxanthylium‐Salzen (I) erhält man mit den Aminen (II) die entsprechenden Benzacridinium‐Salze (III), die thermisch zu den Olefinen (IV) gespalten werden.
    Primary (astronomy)
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    Abstract Primary aliphatic amines are good nucleophilic reagents which easily react with dichloroacetylene (DCA). The reactions of DCA with primary aliphatic amines have been studied and a mechanism of these reactions has been proposed and discussed.
    Primary (astronomy)
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    Abstract A new method has been developed for the selective conversion of primary aliphatic amines into unsymmetrical secondary amines by Grignard reaction of 1‐[(alkylamino)methyl]‐benzotriazoles 1 . This method employs simple procedure and mild conditions, and is specific in that only monoalkylation of the primary amines results.
    Primary (astronomy)
    Substitution (logic)
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