Yu, Lu published the artcileRegio- and Enantioselective Formal Hydroamination of Enamines for the Synthesis of 1,2-Diamines, Product Details of C9H10O3, the main research area is regioselective enantioselective hydroamination enamine diamine synthesis; amines; copper; enamines; enantioselectivity; hydroamination.
The asym. formal hydroamination of enamines using a CuH catalyst is reported [e.g., enamine I + O-acylhydroxylamine II → diamine III (69%, 97:3 e.r.) in presence of (MeO)2MeSiH as hydride source, Cu(OAc)2 and (R)-DTBM-SEGPHOS]. The method provides a straightforward and efficient approach to the synthesis of chiral 1,2-dialkyl amines in good yields with high levels of enantioselectivities for a broad range of substrates, and should have significant value for the preparation of mols. bearing a 1,2-diamine motif.
Angewandte Chemie, International Edition published new progress about Diamines Role: SPN (Synthetic Preparation), PREP (Preparation) (chiral). 104-01-8 belongs to class isoquinoline, name is 4-Methoxyphenylacetic acid, and the molecular formula is C9H10O3, Product Details of C9H10O3.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem