A new synthetic route of 1260795-42-3

From this literature《Highly Enantioselective Synthesis of 2,3-Dihydro-1H-imidazo[2,1-a]isoindol-5(9bH)-ones via Catalytic Asymmetric Intramolecular Cascade Imidization-Nucleophilic Addition-Lactamization》,we know some information about this compound(1260795-42-3)Application In Synthesis of Methyl 4-bromo-2-formylbenzoate, but this is not all information, there are many literatures related to this compound(1260795-42-3).

Application In Synthesis of Methyl 4-bromo-2-formylbenzoate. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: Methyl 4-bromo-2-formylbenzoate, is researched, Molecular C9H7BrO3, CAS is 1260795-42-3, about Highly Enantioselective Synthesis of 2,3-Dihydro-1H-imidazo[2,1-a]isoindol-5(9bH)-ones via Catalytic Asymmetric Intramolecular Cascade Imidization-Nucleophilic Addition-Lactamization.

Highly enantioselective catalytic asym. intramol. cascade imidization-nucleophilic addition-lactamization of N1-alkylethane-1,2-diamine with Me 2-formylbenzoate catalyzed by a chiral phosphoric acid represents the first efficient method for the preparation of medicinally interesting chiral 2,3-dihydro-1H-imidazo[2,1-a]isoindol-5(9bH)-ones, e.g., I, with high yields and excellent enantioselectivities. This strategy has been shown to be quite general toward various Me 2-formylbenzoates.

From this literature《Highly Enantioselective Synthesis of 2,3-Dihydro-1H-imidazo[2,1-a]isoindol-5(9bH)-ones via Catalytic Asymmetric Intramolecular Cascade Imidization-Nucleophilic Addition-Lactamization》,we know some information about this compound(1260795-42-3)Application In Synthesis of Methyl 4-bromo-2-formylbenzoate, but this is not all information, there are many literatures related to this compound(1260795-42-3).

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem