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  2. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    A protecting group or protective group is introduced into a molecule by ... Allyl esters — As with allyl ethers, also ... New Jersey, ISBN 0-471-69754 ...

  3. 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 ...

  4. Nucleoside phosphoramidite - Wikipedia

    en.wikipedia.org/wiki/Nucleoside_phosphoramidite

    In the second, mild protection scheme, A and dA are protected with isobutyryl [28] or phenoxyacetyl groups (PAC). [29] C and dC bear acetyl protection, [27] and G and dG are protected with 4-isopropylphenoxyacetyl (i-Pr-PAC) [30] or dimethylformamidino (dmf) [31] groups. Mild protecting groups are removed more readily than the standard ...

  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. 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

  7. 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). ...

  8. Goose protecting its brood causing problems at NJ diner - AOL

    www.aol.com/news/goose-protecting-brood-causing...

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  9. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    The allyloxycarbonyl (alloc) protecting group is sometimes used to protect an amino group (or carboxylic acid or alcohol group) when an orthogonal deprotection scheme is required. It is also sometimes used when conducting on-resin cyclic peptide formation, where the peptide is linked to the resin by a side-chain functional group.