Research speed reading in 2021. An article , which mentions Product Details of 118864-75-8, molecular formula is C15H15N. The compound – (S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline played an important role in people’s production and life., Product Details of 118864-75-8
A catalysed two-way enantioselective synthesis of chiral tetrahydroisoquinoline method, the catalyzing system is iridium chiral double phosphine complexes. The use of sole chiral source, to the reaction system through the achiral additive consumption of N – bromosuccinimide adjusting, realizes the simple and easily obtained 3, 4 – ISO-quinoline substrate of the asymmetric hydrogenation. The method utilizes a sole chiral source respectively to obtain the corresponding chiral tetrahydroisoquinoline of two enantiomers, its enantiomeric excess highest respectively reaches 89% (S) and 98% (R). The operation of the invention is simple and practical and easy, simple and easy to obtain raw materials, catalyst commercial available, mild reaction conditions, high yield, high enantioselectivity. In addition, only through non-chiral additive conditions, can obtain the tetrahydroisoquinoline of two enantiomers, successfully avoids the two different configuration ligand. (by machine translation)
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 118864-75-8, and how the biochemistry of the body works.Product Details of 118864-75-8
Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem