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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...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  4. File:PMB deprotection.svg - Wikipedia

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

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  5. 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 ]

  6. Category : Citation and verifiability maintenance templates

    en.wikipedia.org/wiki/Category:Citation_and...

    These templates relate to the verifiability of Wikipedia articles, or their lack thererof. This includes the use of citations and reliable sources. See Wikipedia:Template messages/Sources of articles for guides to usage of some of these templates.

  7. 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.

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