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  2. Di-tert-butyl dicarbonate - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_dicarbonate

    Di-tert-butyl dicarbonate is a reagent widely used in organic synthesis. [1] Since this compound can be regarded formally as the acid anhydride derived from a tert-butoxycarbonyl (Boc) group, it is commonly referred to as Boc anhydride. This pyrocarbonate reacts with amines to give N-tert-butoxycarbonyl or so-called Boc

  3. tert-Butyloxycarbonyl protecting group - Wikipedia

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

    tert-Butyloxycarbonyl protecting group. The tert-butyloxycarbonyl protecting group or tert-butoxycarbonyl protecting group [1] (BOC group) is an acid-labile protecting group used in organic synthesis. The BOC group can be added to amines under aqueous conditions using di-tert-butyl dicarbonate in the presence of a base such as sodium hydroxide:

  4. Tris(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate - Wikipedia

    en.wikipedia.org/wiki/Tris(3,5-di-tert-butyl-4...

    Tris(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate is a chemical compound used as a polymer stabilizer in plastics. Like other hindered phenols it acts as a primary antioxidant. More than 1000 tonnes per year are used in the EU.

  5. Category:Tert-butyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Tert-butyl_compounds

    4-tert-Butylcatechol; Tert-Butyldiphenylsilyl; Tert-Butylhydroquinone; Tert-Butyllithium; Tert-Butyloxycarbonyl protecting group; Tert-Butylphosphaacetylene; Tert-Butylthiol; N-t-Butyltryptamine; Butyrolactol A

  6. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    The tert-butyloxycarbonyl group is marked blue. Amines have a special importance in peptide synthesis, but are a quite potent nucleophile and also relatively strong bases. These characteristics imply that new protecting groups for amines are always under development. [47] Amine groups are primarily protected through acylation, typically as a ...

  7. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

  8. Strecker amino acid synthesis - Wikipedia

    en.wikipedia.org/wiki/Strecker_amino_acid_synthesis

    "Boc" is tert-Butyloxycarbonyl protecting group. Catalytic asymmetric Strecker reaction can be effected using thiourea-derived catalysts. [7] In 2012, a BINOL-derived catalyst was employed to generate chiral cyanide anion (see figure). [8]

  9. Dicarbonate - Wikipedia

    en.wikipedia.org/wiki/Dicarbonate

    di-tert-butyl dicarbonate (H 3 C−) 3 C−C 2 O 5 −C(−CH 3) 3, also known as Boc anhydride. It is one of the oxocarbon anions, consisting solely of oxygen and carbon. The anion has the formula − O−C(=O)−O−C(=O)−O − or C 2 O 2− 5. Dicarbonate salts are apparently unstable at ambient conditions, but can be made under pressure ...

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