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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. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    Orthogonal protection is a strategy allowing the specific deprotection of one protective group in a multiply-protected structure. For example, the amino acid tyrosine could be protected as a benzyl ester on the carboxyl group, a fluorenylmethylenoxy carbamate on the amine group, and a tert-butyl ether on the phenol

  4. tert-Butyloxycarbonyl protecting group - Wikipedia

    en.wikipedia.org/wiki/Tert-butyloxycarbonyl...

    [5] [6] Selective cleavage of the N-Boc group in the presence of other protecting groups is possible when using AlCl 3. Sequential treatment with trimethylsilyl iodide then methanol can also be used for Boc deprotection, [7] [8] especially where other deprotection methods are too harsh for the substrate. [9]

  5. File:PMB deprotection mechanismn.svg - Wikipedia

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

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  6. Photolabile protecting group - Wikipedia

    en.wikipedia.org/wiki/Photolabile_protecting_group

    As a second example, researchers synthesized a cycloprene-modified glutamate photocaged with a 2-nitroveratrol-based PPG. As it is an excitatory amino acid neurotransmitter, the aim was to develop a bioorthagonal probe for glutamate in vivo. [47] In a final example, Venkatesh et al. demonstrated the use of a PPG-based photocaged therapeutic. [48]

  7. Trimethylsilyl trifluoromethanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_trifluorome...

    Deprotection of Boc-protected amines can be achieved using trimethylsilyl trifluoromethanesulfonate and triethylamine or 2,6-lutidine. [7] [8] TMSOTf is also a useful reagent to replace metal-halogen bonds with a covalent M-O(SO2CF3) bond, the by-product being the highly volatile TMSCl which is easily removed.

  8. 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.

  9. 1,4-Benzoquinone - Wikipedia

    en.wikipedia.org/wiki/1,4-Benzoquinone

    1,4-Benzoquinone, commonly known as para-quinone, is a chemical compound with the formula C 6 H 4 O 2.In a pure state, it forms bright-yellow crystals with a characteristic irritating odor, resembling that of chlorine, bleach, and hot plastic or formaldehyde.

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