1 s with a novel reagent, 2,4-dibromo-(2'-iodo)acetanilide.

2  as the preferred conformational lock of the acetanilide.

3 to be higher than those of the corresponding acetanilides.

4  biphenyls, aromatic amines, and substituted acetanilides.

5                                              Acetanilides 1a-e react with 1,1'-sulfinylbis(benzotriaz

6 ive hydroarylation reactions between diverse acetanilides and aryl- or alkyl-substituted alkenes.

7 eneral for a wide range of anisole, aniline, acetanilide, and phenol derivatives and allowed the late

8 ination of a wide range of anisole, aniline, acetanilide, and phenol derivatives.

9     By this protocol, various heteroarylated acetanilide derivatives are synthesized in good yields.

10 be new 1-(omega-phenoxyalkyl)uracils bearing acetanilide fragment in 3 position of pyrimidine ring as

11 e feasible through the introduction of a new acetanilide substrate analogue of acetylcholine, 3-(acet

12 reaction provides efficient access to o-acyl acetanilides under mild conditions.

13      A series of conformationally restricted acetanilides were synthesized and evaluated as beta3-adr

14 catalyzed decarboxylative ortho-acylation of acetanilides with alpha-oxocarboxylic acids is realized