ライフサイエンスコーパス: iodobenzene

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1 s an oxidant can be efficiently catalyzed by iodobenzene.

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

3 lsulfonic acids in the presence of diacetoxy iodobenzene.

4 te for the initiation of phenyl radical from iodobenzene.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

22 1 and 7 underwent oxidative cyclization with iodobenzene diacetate or iodosobenzene in the presence o

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

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

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

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

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

28 Iodobenzene is found to have no effect and thus probably

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

30 4 via Sonogashira couplings with appropriate iodobenzenes or phenylacetylene followed by reduction an

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

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

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

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

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

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

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

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

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

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

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