(2R)-2-PHENYL-3,4-DIHYDRO-2H-PYRIMIDO[2

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

This chiral isothiourea homobenzotetramisole ((R)-HBTM) developed by the Birman lab is an organocatalyst that has been used for kinetic resolution, determination of absolute configuration, and nucleophile-catalysed, Michael–aldol-b-lactonization (NCMAL). This same product was previously listed as L511730, and the complementary (S)-HBTM organocatalyst (900542) is also available.

Other Notes

Technology Spotlight: Homobenzotetramisole (HBTM): A General Organocatalyst for Asymmetric Acylations[1] Determination of the Absolute Configuration β-Chiral Primary Alcohols Using the Competing Enantioselective Conversion Method[2] Asymmetric Catalytic Synthesis of Thiochromenes via an Acyl Transfer-Initiated Cascade[3] Rapid assembly of complex cyclopentanes employing chiral, α, β-unsaturated acylammonium intermediates[4] Determination of Absolute Configuration Using Kinetic Resolution Catalysts[5] Kinetic Resolution of Secondary Alcohols Using Amidine-Based Catalysts