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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. Windows 11, version 24H2 - Wikipedia

    en.wikipedia.org/wiki/Windows_11,_version_24H2

    Windows 11 Search adds the ability to search for documents and photos using descriptive phrases instead of just file names. [14] Super Resolution: photographs may now be enhanced up to 8x without sacrificing quality using AI upscaling, which works faster on Copilot+ PCs. [15] Windows Recall (preview) which lets users find content they have ...

  4. File:PMB deprotection mechanismn.svg - Wikipedia

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

    File:PMB deprotection mechanismn.svg. ... Download QR code; In other projects ... The following 2 pages use this file: Protecting group;

  5. File:PMB deprotection.svg - Wikipedia

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

    File:PMB deprotection.svg. Add languages. Page contents not supported in other languages. ... Download QR code; In other projects Appearance. move to sidebar hide

  6. Chloranil - Wikipedia

    en.wikipedia.org/wiki/Chloranil

    It is also a good test for the successful deprotection of a secondary amine. Secondary amines react with chloranil to give a brown/red/orange derivative, the colour depending on the amine. In these reactions, the amine displaces chloride from the ring of the quinone.

  7. 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 ]

  8. 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.

  9. Photolabile protecting group - Wikipedia

    en.wikipedia.org/wiki/Photolabile_protecting_group

    The first reported use of a PPG in the scientific literature was by Barltrop and Schofield, who in 1962 used 253.7 nm light to release glycine from N-benzylglycine. [4] Following this initial report, the field rapidly expanded throughout the 1970s as Kaplan [ 6 ] and Epstein [ 7 ] studied PPGs in a variety of biochemical systems.