A facile synthesis of telisatin A via microwave-promoted annulation and Reformatsky reaction was written by Thasana, Nopporn;Bjerke-Kroll, Ben;Ruchirawat, Somsak. And the article was included in Synlett in 2008.Safety of 6,7-Dimethoxy-3,4-dihydroisoquinoline This article mentions the following:
A facile one-pot synthesis of 2,3-dioxopyrrolo[2,1-a]isoquinolines was reported involving the ring formation of aryl pyruvate derivatives with 3,4-dihydroisoquinolines under basic conditions and utilizing the Reformatsky reaction. Using microwave irradiation, the required compounds were obtained in moderate to good yields. In the experiment, the researchers used many compounds, for example, 6,7-Dimethoxy-3,4-dihydroisoquinoline (cas: 3382-18-1Safety of 6,7-Dimethoxy-3,4-dihydroisoquinoline).
6,7-Dimethoxy-3,4-dihydroisoquinoline (cas: 3382-18-1) belongs to isoquinoline derivatives. Quinoline is a mancude organic heterobicyclic parent, an azaarene, an ortho-fused heteroarene and a member of isoquinolines. The discovery of chloroquine, the most well-known drug containing this stent, has helped bring about decades of malaria control and treatment.Safety of 6,7-Dimethoxy-3,4-dihydroisoquinoline
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem