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 ange of arenes, including anisoles, phenols, acetanilides, and N-heterocycles.

10  were rapidly metabolized, the more stable p-acetanilide cleared 99.7% of parasites at 4 x 50 mg kg(-

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

12 , dimethyl sulfone, 1,3,5-trimethoxybenzene, acetanilide, dimethyl terephthalate, and 1,2,4,5-tetrame

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

14 secondary N-H amides, including benzanilide, acetanilide, oxindole, isatin, quinolinone, and maleimid

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

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

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

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

19 f aniline with CO, resulting in a remarkable acetanilide yield rate of 1021.2 mmol h(-1) g(cat.) (-1)