ライフサイエンスコーパス: iodobenzene

1 ides under ambient air using PIDA (diacetoxy iodobenzene).

2 s an oxidant can be efficiently catalyzed by iodobenzene.

3 turber, whereas the steady-state method used iodobenzene.

4 lsulfonic acids in the presence of diacetoxy iodobenzene.

5 of amido-urea precursors, using bis(acetoxy)iodobenzene.

6 te for the initiation of phenyl radical from iodobenzene.

7 ethyl 3-(benzoyloxy)-8-2-(4-azido-3-[ (125)I]iodobenzene)-1-ethyl-8-azabicyclo[3.2.1]octane-2-carboxy

8 Z = NH2 (10)), 4-iodoacetophenone (11), and iodobenzene (12) were measured in CDCl(3), DMSO, THF, py

9 -bis(ethynyl)porphyrinate) with N, N'-bis( p-iodobenzene)-2,3,5,6-tetrafluorobenzoquinone-1,4-diimine

10 roxy-2(5H)-furanone (7) with 2-((2Z)-hexenyl)iodobenzene (8d) followed by Lindlar catalyzed hydrogena

11 terionic species, and subsequent ejection of iodobenzene, affords the lactone and aurone cycloadducts

12 An efficient synthesis of 1-(S-acetylthio)-4-iodobenzene also has been developed.

13 not limited to reactions of carbazoles with iodobenzene and alkyl halides.

14 nds are maintained for electronically biased iodobenzene and bromobenzene electrophiles.

15 s to give iodonium ions, which rapidly expel iodobenzene and undergo different subsequent reactions.

16 The Cu(I)-catalyzed reaction of 1-bromo-2-iodobenzenes and other 1,2-dihalobenzenes with 1,3-cyclo

17 ccessible by employing substituted 1-bromo-2-iodobenzenes and substituted 1,3-cyclohexanediones as su

18 odobenzene diacetate, [bis(trifluoroacetoxy)]iodobenzene, and ammonium cerium(IV) nitrate in acetonit

19 reaction requires as little as 0.5 mol % of iodobenzene, and its scope is broad: electron-withdrawin

20 n of polychlorinated benzenes, bromobenzene, iodobenzene, and selected mixed dihalobenzenes.

21 F(6) ] is shown to react quantitatively with iodobenzenes (ArI(n) , n=1,2) to yield [CpRu(eta(6) -ArI

22 -piperidin-1-yl)oxyl (TEMPO) and bis(acetoxy)iodobenzene (BAIB).

23 g reactions of methanol and methylamine with iodobenzene by beta-diketone- and 1,10-phenanthroline-li

24 rgylic alcohol 8 was prepared from 1-bromo-2-iodobenzene by two consecutive Sonogashira cross-couplin

25 zuki reaction between phenylboronic acid and iodobenzene catalyzed by PVP-Pd nanoparticles to investi

26 n of 2-amino-4H-pyrans was accomplished with iodobenzene diacetate (IBD) and N-chlorosuccinimide (NCS

27 iodosylbenzene (PhIO) or the combination of iodobenzene diacetate (PIDA)/molecular iodine (I2), unde

28 r)(2) formed through ligand exchange between iodobenzene diacetate and arylglyoxylic acid to initiate

29 1 and 7 underwent oxidative cyclization with iodobenzene diacetate or iodosobenzene in the presence o

30 nditions involving the stable and recyclable iodobenzene diacetate reagent are compatible with a rang

31 on of corresponding N-hydroxy compounds with iodobenzene diacetate, [bis(trifluoroacetoxy)]iodobenzen

32 This protocol utilizes a combination of an iodobenzene dicarboxylate and iodine to functionalize a

33 reating diazoacetate derivatives with either iodobenzene dichloride or iodotoluene difluoride results

34 acetonitrile] with the pyridinium complex of iodobenzene ditriflate or with [hydroxy(tosyloxy)iodo]be

35 C(sp(3))-H of aryl-2H-azirine and (diacetoxy)iodobenzene has been reported.

36 The rate of amination of iodobenzene in liquid ammonia is first order in copper(I

37 ho = 0.49 for the amination of 4-substituted iodobenzenes in liquid ammonia at 25 degrees C indicates

38 s then used to demonstrate the conversion of iodobenzene into its biphenyl product (confirmed through

39 Iodobenzene is found to have no effect and thus probably

40 C7,C7'-stereochemistry, bis(trifluoroacetoxy)iodobenzene mediated oxygenation, a palladium-catalyzed

41 Addition of iodobenzene or bromobenzene to (3,5-Me(2)(Mes)CNC)Fe(N(2

42 4 via Sonogashira couplings with appropriate iodobenzenes or phenylacetylene followed by reduction an

43 ion between potassium thioacetate (KSAc) and iodobenzene (PhI) catalyzed by CuI associated with 1,10-

44 (Diacetoxy)iodobenzene (PIDA)-mediated direct oxidative C-H aminati

45 ion of the isomers with bis(trifluoroacetoxy)iodobenzene (PIFA) leads to rapid formation of new highl

46 The effect of iodobenzene substituents was also studied with surprisin

47 In addition to the model ethanolamine/iodobenzene system, various heteroaromatic substrates an

48 ator, and a set of five fluorine-substituted iodobenzenes that take the role of the stator.

49 barriers for both the oxidative addition of iodobenzene to [(DMF)CuCF(2)CN] and the reductive elimin

50 f phthalic anhydride to benzyne, cleavage of iodobenzene to phenyl radical, aryl-aryl bond cleavage,

51 gand coupling, with reductive elimination of iodobenzene to yield the product.

52 nts of the model oxidants (cumyl alcohol and iodobenzene) to the reductase-supported system did not a

53 ptides (L9G and L9A) bind the small molecule iodobenzene when present during crystallization, leaving

54 The reaction of o-(allyloxy)iodobenzene with [(phen) 2Cu][Cu(pyrr) 2] results in for

55 The reaction order was determined for iodobenzene (zero order), indole (first order), and the