1267460-80-9

Upstream product

• 615-43-0 2-iodophenylamine 
• 13141-38-3 2-phenylethynylaniline 
• 104682-98-6 N-(2-(2-phenylethynyl)phenyl)benzamide 
• 536-74-3 phenylacetylene 
• 15310-02-8 o-iodobenzanilide 
• 98-88-4 benzoyl chloride 

Relevant academic research and scientific papers

Iodine-catalyzed, stereo- and regioselective synthesis of 4-arylidine-4H-benzo[d][1,3]oxazines and their applications for the synthesis of quinazoline 3-oxides

4-Benzylidene-2-aryl-4H-benzo[d][1,3] oxazines have been synthesized with high stereoselectivity and regioselectivities from 2-alkynylbenzamides in the presence of a catalytic amount of I2. In the reaction mechanism, iodine plays a key role in

Palladium-catalyzed highly regio-and stereoselective synthesis of 4-alkylidene-4 H -3,1-benzoxazines from N -Acyl-o -alkynylanilines

The highly regio-and stereoselective 6-exo-dig mode cyclization of N-acyl-o-alkynylanilines producing 4-alkylidene-3,1-benzoxazines occurred unpredictably by use of a proper catalyst [Pd(OAc)2] and an effective additive (acetic acid) under suit