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  2. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.

  3. Benzil - Wikipedia

    en.wikipedia.org/wiki/Benzil

    The compound's most noteworthy structural feature is the long carbon-carbon bond of 1.54 Å, which indicates the absence of pi-bonding between the two carbonyl centers.The PhCO centers are planar, but the pair of benzoyl groups are twisted with respect to the other with a dihedral angle of 117°. [5]

  4. Benzylisoquinoline - Wikipedia

    en.wikipedia.org/wiki/Benzylisoquinoline

    S)-Norcoclaurine has been identified as the central 1-benzyl-tetrahydro-isoquinoline precursor [1] [2] from which numerous complex biosynthetic pathways eventually emerge. These pathways collectively lead to the structurally disparate compounds comprising the broad classification of plant natural products referred to as benzylisoquinoline ...

  5. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine is used as a masked source of ammonia, since after N-alkylation, the benzyl group can be removed by hydrogenolysis: [10] C 6 H 5 CH 2 NH 2 + 2 RBr → C 6 H 5 CH 2 NR 2 + 2 HBr C 6 H 5 CH 2 NR 2 + H 2 → C 6 H 5 CH 3 + R 2 NH. Typically a base is employed in the first step to absorb the HBr (or related acid for other kinds of ...

  6. Benzylisoquinoline alkaloids - Wikipedia

    en.wikipedia.org/wiki/Benzylisoquinoline_alkaloids

    Over 2500 biologically active derivatives are known from the benzylisoquinoline alkaloids. [4] Based on their structure, the compounds can be divided into numerous subgroups: the aporphines, the phthalideisoquinoline alkaloids, the morphinans, the protoberberine alkaloids, and the pavins.

  7. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    For example, the amino acid tyrosine could be protected as a benzyl ester on the carboxyl group, a fluorenylmethylenoxy carbamate on the amine group, and a tert-butyl ether on the phenol group. The benzyl ester can be removed by hydrogenolysis, the fluorenylmethylenoxy group (Fmoc) by bases (such as piperidine), and the phenolic tert-butyl ...

  8. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol is used effectively for treating lice infestations as the active ingredient in lotion shampoo with 5% benzyl alcohol. [13] Benzyl alcohol is an ingredient used in the manufacture of soaps, topical creams, skin lotions, shampoos, and facial cleansers and is popular due to its anti-bacterial and anti-fungal properties.

  9. Benzylidene compounds - Wikipedia

    en.wikipedia.org/wiki/Benzylidene_compounds

    Benzylidene acetal is a protecting group in synthetic organic chemistry of the form PhCH(OR) 2. For example, 4,6-O-benzylidene-glucopyranose is a glucose derivative. Benzylidene is an archaic term for compounds of the type PhCHX 2 and PhCH= substituents (Ph = C 6 H 5). For example, dibenzylideneacetone is (PhCH=CH) 2 CO.