Iodoacetyl chloride

Saima confirmed that 132 was readily obtained in ether in the cold. Sanna also prepared 3-bromoacetylindole (133) and 3-iodoacetylindole (134) by the action of bromoacetyl chloride and iodoacetyl chloride, respectively, on the indole Grignard reagent.The corresponding... 

Chloracetyl-p-arsanilic acid is prepared by the interaction of chloracetyl chloride and p-arsanilic acid, whilst the corresponding iodoacetyl derivative (M.pt. 196° C.) and the iodopropionyl derivative (M.pt. 224° C.) are formed by treating sodium hydroxide solutions of the acid with the respective acid chloride. ... 

Tri-0-benzyl-l-(9-iodoacetyl-D-ribofuranose (a/p = 1/5) gave the best results as a glycosyl donor in the synthesis of both a and P ribofuranosides the combined use of silver perchlorate and lithium perchlorate afforded ribofuranosides with high a stereoselectivity. On the other hand, P-ribosides were obtained with different catalytic systems, such as the combination of silver perchlorate and di-phenyltin sulfide. The milder tin(II) chloride also gave high yields of P-ribosides, when used in combination with 2 mol% of tetrachlorosilane [97]. 

Iodoacetylamino)pyrene, see 1-00051 lodoacetyl chloride, in 1-00036 A -(Iodoacetyl)-l-pyrenamine, see 1-00051 lodobenzene bis(trifluoroacetate), see B-00462 lodobenzene 1,1-ditrifluoroacetate, see... 

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