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  2. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    Protecting groups are more common in small-scale laboratory work and initial development than in industrial production because they add additional steps and material costs. However, compounds with repetitive functional groups – generally, biomolecules like peptides , oligosaccharides or nucleotides – may require protecting groups to order ...

  3. Tsuji–Trost reaction - Wikipedia

    en.wikipedia.org/wiki/Tsuji–Trost_reaction

    The Tsuji–Trost reaction (also called the Trost allylic alkylation or allylic alkylation) is a palladium-catalysed substitution reaction involving a substrate that contains a leaving group in an allylic position. The palladium catalyst first coordinates with the allyl group and then undergoes oxidative addition, forming the π-allyl

  4. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    In organic chemistry, an allyl group is a substituent with the structural formula −CH 2 −HC=CH 2. It consists of a methylene bridge (−CH 2 −) attached to a vinyl group (−CH=CH 2). [1] [2] The name is derived from the scientific name for garlic, Allium sativum. In 1844, Theodor Wertheim isolated an allyl derivative from garlic oil and ...

  5. Krische allylation - Wikipedia

    en.wikipedia.org/wiki/Krische_allylation

    The excellent functional group compatibility of the Krische allylation combined with the tractability of the allyl acetate pronucleophiles enables the use of allyl donors bearing highly complex nitrogen-rich substituents. [20] insert a caption here. The figure below shows some of the different allyl donors that have been used in the Krische ...

  6. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    The solid support consists of small, polymeric resin beads functionalized with reactive groups (such as amine or hydroxyl groups) that link to the nascent peptide chain. [2] Since the peptide remains covalently attached to the support throughout the synthesis, excess reagents and side products can be removed by washing and filtration.

  7. Trimethylsilyl group - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_group

    When attached to certain functional groups in a reactant molecule, trimethylsilyl groups may also be used as temporary protecting groups during chemical synthesis or some other chemical reactions. In chromatography, derivitization of accessible silanol groups in a bonded stationary phase with trimethylsilyl groups is referred to as endcapping.

  8. Category:Allyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Allyl_compounds

    Pages in category "Allyl compounds" The following 114 pages are in this category, out of 114 total. ... Allyl group; Allyl hexanoate; Allyl iodide; Allyl isothiocyanate;

  9. Category:Protecting groups - Wikipedia

    en.wikipedia.org/wiki/Category:Protecting_groups

    Thermolabile protecting groups; 2,2,2-Trichloroethoxycarbonyl chloride This page was last edited on 15 September 2015, at 12:37 (UTC). ...