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  2. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichloro-5,6-dicyano-1...

    2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (or DDQ) is the chemical reagent with formula C 6 Cl 2 (CN) 2 O 2. This oxidant is useful for the dehydrogenation of alcohols, [3] phenols, [4] and steroid ketones. [5] DDQ decomposes in water, but is stable in aqueous mineral acid. [6]

  3. File:PMB deprotection mechanismn.svg - Wikipedia

    en.wikipedia.org/wiki/File:PMB_deprotection...

    Original file (SVG file, nominally 1,119 × 311 pixels, file size: 51 KB) This is a file from the Wikimedia Commons . Information from its description page there is shown below.

  4. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    p-Methoxybenzyl (PMB) is used as a protecting group for alcohols in organic synthesis (4-Methoxybenzylthiol is used to protect thiols). The p -methoxybenzyl group Strong base such as powdered potassium hydroxide or sodium hydride and p -methoxybenzyl halide (chloride or bromide) [ 14 ] [ 15 ]

  5. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    The use of protective groups is pervasive but not without criticism. [103] In practical terms their use adds two steps (protection-deprotection sequence) to a synthesis, either or both of which can dramatically lower chemical yield. Crucially, added complexity impedes the use of synthetic total synthesis in drug discovery.

  6. File:PMB deprotection.svg - Wikipedia

    en.wikipedia.org/wiki/File:PMB_deprotection.svg

    Original file (SVG file, nominally 1,020 × 454 pixels, file size: 92 KB) This is a file from the Wikimedia Commons . Information from its description page there is shown below.

  7. File:D-Codes.pdf - Wikipedia

    en.wikipedia.org/wiki/File:D-Codes.pdf

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  8. Trichloroethyl chloroformate is used in organic synthesis for the introduction of the trichloroethyl chloroformate (Troc) protecting group for amines, thiols and alcohols.It readily cleaves vs other carbamates and can be used in an overall protecting group strategy.

  9. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    Desulfonylation reactions are chemical reactions leading to the removal of a sulfonyl group from organic compounds.As the sulfonyl functional group is electron-withdrawing, [1] methods for cleaving the sulfur–carbon bonds of sulfones are typically reductive in nature.