Iodine-mediated electrophilic cyclization of 2-alkynylbenzaldoximes leading to the formation of iodoisoquinoline N-oxides
-
Add time:08/31/2019 Source:sciencedirect.com
Reaction of 2-alkynylbenzaldoximes 1 with 5 equiv of iodine in EtOH at room temperature gives the corresponding iodoisoquinoline N-oxides 2 in good to excellent yields. The cyclization proceeds very smoothly and quickly without any additives such as bases under very mild reaction conditions.
We also recommend Trading Suppliers and Manufacturers of 1-IODOISOQUINOLINE (cas 19658-77-6). Pls Click Website Link as below: cas 19658-77-6 suppliers
Prev:Consecutive SRN1 and ERC1 reactions in 5-nitroisoquinolines
Next:Research paperMode of hydrophilic and hydrophobic interactions of DL-Tyrosine, DL-Leucine, DL-Isoleucine and DL-Threonine in aqueous binary mixture of dipolar aprotic Acetonitrile) - 【Back】【Close 】【Print】【Add to favorite 】


