𝘕,𝘕'-Diisopropyl-𝙊-𝙩𝙚𝙧𝙩-butyl isourea: an efficient reagent for 𝙩𝙚𝙧𝙩-butyl esters synthesis

tert-Butyl esters are commonly used as protecting group of carboxylic acids in multi-step synthesis, especially with amino acids, peptides and natural products. [1] The importance of this relatively hindered protecting group is well established.

tert-Butyl Nitrite-Mediated Synthesis of N-Nitrosoamides, Carboxylic Acids, Benzocoumarins, and Isocoumarins from Amides

An efficient synthesis of α-deuterated carboxylic acids

Organic Syntheses Procedure

Tert-Butylation - an overview

Efficient and Controllably Selective Preparation of Esters Using Uronium-Based Coupling Agents

An efficient synthesis of α-deuterated carboxylic acids

An efficient synthesis of N-tert-butyl amides by the reaction of tert-butyl benzoate with nitriles catalyzed by Zn(ClO4)2·6H2O

Approaches for the Synthesis of Functionalized Cryptophycins

Enantioselective Total Syntheses of Cyathane Diterpenoids - Nakada - 2014 - The Chemical Record - Wiley Online Library

Uses for Akanocure Stereotetrad Lactones 5a: Full Lactone Reductions

Full article: Preparation and Applications of 4-Methoxybenzyl Esters in Organic Synthesis

Full article: Preparation and Applications of 4-Methoxybenzyl Esters in Organic Synthesis

ZnEt2 as a Precatalyst for the Addition of Alcohols to Carbodiimides

Enantioselective Total Syntheses of Cyathane Diterpenoids - Nakada - 2014 - The Chemical Record - Wiley Online Library