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2. 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.

3. tert-Butyl alcohol - Wikipedia

   en.wikipedia.org/wiki/Tert-Butyl_alcohol

   tert-Butyl alcohol is used as a solvent, ethanol denaturant, paint remover ingredient, and gasoline octane booster and oxygenate.It is a chemical intermediate used to produce methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) by reaction with methanol and ethanol, respectively, and tert-butyl hydroperoxide (TBHP) by reaction with hydrogen peroxide.

4. Category:Tert-butyl compounds - Wikipedia

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

   Tert-Butyl bromide; Tert-Butyl chloride; Tert-Butyl hydroperoxide; Tert-Butyl isocyanide; Butyl PBD; Tert-Butylamine; Butylated hydroxyanisole; Butylated hydroxytoluene; 4-tert-Butylbenzaldehyde; N-tert-Butylbenzenesulfinimidoyl chloride; Para-tert-Butylbenzoic acid; 4-tert-Butylcatechol; Tert-Butyldiphenylsilyl; Tert-Butylhydroquinone; Tert ...

5. tert-Butyldiphenylsilyl - Wikipedia

   en.wikipedia.org/wiki/Tert-Butyldiphenylsilyl

   The tert-butyldiphenylsilyl group was first suggested as a protecting group by Hanessian and Lavallée in 1975. It was designed to supersede the use of Corey's tert-butyldimethylsilyl as a protecting group for alcohols:

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