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10.10- diiodo

A novel and highly efficient synthesis of 1,1-diiodo-, 1,1-dibromo-, and mixed (Z)- or ( )-1-iodo-l-bromo-l-alkenes using the 1,1-heterobimetallic reagents obtained by hydrozirconation of stannylacetylenes has also been described [155], The hydrozirconation and halo-genolysis steps were carried out at room temperature in THF under a nitrogen atmosphere. It is noteworthy that the developed route is compatible with various functionalities... [Pg.257]

A synthesis of potentially useful 1-iodo-l-bromo-l-alkenes has thus been developed that offers complete stereocontrol. These methods have also proven to be highly efficient for the preparation of 1,1-diiodo-l-alkenes and 1,1-dibromo-l-alkenes, which are very useful synthetic intermediates (Scheme 7.26) [155]. [Pg.260]

Diiodine trioxide, derivatives of, 5 76-77 1,1 -Diiodo-3,4-benzo-1 -telluracyclopentane, 35 246... [Pg.80]

The second approach to the preparation of 1-telluracyclohexane involves the reaction of 1,5-diiodopentane with elemental tellurium under heating (45JCS11). Initially formed (in 63% yield) 1,1-diiodo-l-telluracyclohexane 6 (X = I) is readily reduced to 1 by potassium metabisulfite in almost quantitative yield. [Pg.4]

Soc. Perkin Trans. 11998, 2413-2423. Barluenga, J. Rodriguez, M. A. Campos, P. J. Asensio, G. Synthesis of 2-functionalized 1,1-diiodo-l-alkenes. Generation and reactions of... [Pg.222]

Diodo-l-alkenes.1 This reagent (1) in combination with a wide variety of nucleophiles reacts with 1-iodoalkynes to afford 2-substituted 1,1-diiodo-l-alkenes (2) in 50-85% yield. The products can be converted to a variety of alkenes by reaction of both the iodine atoms.2... [Pg.38]

Tcllurolan-diid l,l-Dichloro-1,1-diiodo- El2b, 669(R2TeI2 + Cl )... [Pg.164]

C5H10I2 1,1 -diiodo-2-methylbutane 66688-50-4 499.20 43.345 2 5484 C5H10OS 2-methyltetrahydrofuran-3-thiol, mixed isome 57124-87-5 443.15 38.450 1.2... [Pg.431]


See other pages where 10.10- diiodo is mentioned: [Pg.550]    [Pg.5]    [Pg.217]    [Pg.730]    [Pg.165]    [Pg.224]    [Pg.452]    [Pg.550]    [Pg.12]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.116]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.319]    [Pg.325]    [Pg.325]    [Pg.325]    [Pg.431]    [Pg.431]    [Pg.557]    [Pg.560]    [Pg.560]    [Pg.560]    [Pg.602]    [Pg.605]    [Pg.605]    [Pg.605]   
See also in sourсe #XX -- [ Pg.526 , Pg.557 , Pg.763 , Pg.819 ]

See also in sourсe #XX -- [ Pg.526 , Pg.557 , Pg.763 , Pg.819 ]




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1.1- diiodo adduct with iodine

1.1- diiodo-2,5-dihydro

1.1- diiodo-2-methyl

1.1- diiodo-l-alkenes

1.3- Diiodo-2- propane

1.3- Diiodo-5,5-dimethylhydantoin

10.10- diiodo-2,8-dimethyl

2,5-dideoxy-2,5-diiodo

2,6-Diiodo-/>-nitroaniline

2.6- Diiodo-4-nitrophenol

2.8- dichloro-10,10-diiodo

2.8- difluoro-10,10-diiodo

3,7-Diiodo- pyridine

3.5- Diiodo-L-tyrosine

5,7-Diiodo-8-hydroxyquinoline

5,7-diiodo-3-butoxy-6-fluorone

5.5- diiodo-3,7-dimethyl-10-ethyl

8-Quinolinol, 5,7-diiodo

Acetylene diiodo

Aniline 2,4-diiodo

Benzene 1,2-diiodo-, iridium complex

Benzene, />-diiodo

Butane, 1,4-diiodo

Butane, 1,4-diiodo 1,4-dinitro

Diiodo methane

Diiodo oxide

Diiodo poly

Diiodo rhodium complexes

Diiodo tetrathiafulvalene

Diiodomethane: Methane, diiodo

Ethylene 1,1-diiodo

Hexane, 1,6-diiodo

Imidazole 4.5- diiodo

Molybdenum, diiodo

Nickel diiodo

Phenol 2,4-diiodo

Platinum diiodo

Salicylic 3,5-diiodo

Tungsten diiodo

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