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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

    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.

  4. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    For example, (C 6 H 5)(CH 3) 2 C + is referred to as a "benzylic" carbocation. The benzyl free radical has the formula C 6 H 5 CH 2 • . The benzyl cation or phenylcarbenium ion is the carbocation with formula C 6 H 5 CH + 2 ; the benzyl anion or phenylmethanide ion is the carbanion with the formula C 6 H 5 CH − 2 .

  5. Solid-phase synthesis - Wikipedia

    en.wikipedia.org/wiki/Solid-phase_synthesis

    Solid-phase synthesis is a common technique for peptide synthesis.Usually, peptides are synthesised from the carbonyl group side (C-terminus) to amino group side (N-terminus) of the amino acid chain in the SPPS method, although peptides are biologically synthesised in the opposite direction in cells.

  6. File:PMB deprotection mechanismn.svg - Wikipedia

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

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  7. Voltage-gated proton channel - Wikipedia

    en.wikipedia.org/wiki/Voltage-gated_proton_channel

    Voltage-gated proton channels are ion channels that have the unique property of opening with depolarization, but in a strongly pH-sensitive manner. [1] The result is that these channels open only when the electrochemical gradient is outward, such that their opening will only allow protons to leave cells .

  8. Chloroformate - Wikipedia

    en.wikipedia.org/wiki/Chloroformate

    A simple example is methyl chloroformate, which is commercially available. Chloroformates are used as reagents in organic chemistry. For example, benzyl chloroformate is used to introduce the Cbz (carboxybenzyl) protecting group and fluorenylmethyloxycarbonyl chloride is used to introduce the FMOC protecting group. Chloroformates are popular in ...

  9. Quinone - Wikipedia

    en.wikipedia.org/wiki/Quinone

    An example of 1,4-addition reaction is the addition of hydrogen chloride to form chlorohydroquinone: 1,4-addition reaction of quinone with hydrogen chloride to produce chlorohydroquinone Quinones can undergo Diels–Alder reactions . [ 10 ]