《Natural carbolines inspired the discovery of chiral CarOx ligands for asymmetric synthesis and antifungal leads》 was published in Organic Chemistry Frontiers in 2020. These research results belong to Lai, Jixing; Li, Wei; Wei, Sanyue; Li, Shengkun. Synthetic Route of C7H9BO3 The article mentions the following:
The unprecedented β-CarOx ligands were conceived by the hybridization of alangiobussinine and the privileged pyridine-oxazoline scaffold. It is well performed in the highly enantioselective Pd-catalyzed Michael addition of arylboronic acids to nitrostyrenes and β-substituted cyclic enone (up to 99% ee). The β-CarOx ligands also showed an enhanced antifungal effect compared to alangiobussinine, demonstrating promising antifungal leads against Sclerotinia sclerotiorum. The experimental process involved the reaction of 3-Methoxyphenylboronic acid(cas: 10365-98-7Synthetic Route of C7H9BO3)
3-Methoxyphenylboronic acid(cas: 10365-98-7) belongs to boronic acids. Boronic acids are mild Lewis acids which are generally stable and easy to handle, making them important to organic synthesis.Synthetic Route of C7H9BO3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem