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Olation

Bivalent radicals of the form O—Y—O are named by adding -dioxy to the name of the bivalent radicals except when forming part of a ring system. Examples are —O—CHj—O— (methylene-dioxy), —O—CO—O— (carbonyldioxy), and —O—SOj—O— (sulfonyldioxy). Anions derived from alcohols or phenols are named by changing the final -ol to -olate. [Pg.26]

Chromium(III) Chemistry. The most characteristic reactions of Cr(III) in aqueous solution at >4 pH, eg, in the intestine and blood, and hydrolysis and olation (147). As a consequence, inorganic polymeric molecules form that probably are not able to diffuse through membranes. This may be prevented by ligands capable of competing for coordination sites on Cr(III) (see Coordination compounds) (147). Thus any large fraction of ingested Cr(III) should be absorbed. Chromium (ITT) in the form of GTF may be more efficiendy absorbed. [Pg.387]

Thiatriazolin-5-imines undergo a variety of cycloaddition reactions with the elimination of Nt. 1,3-Dithiolylium-4-olates undergo cycloaddition reactions, e.g. as in Scheme 36 80AHC(27)i5l). Scheme 37 gives an example of cycloaddition in the oxathiazole series. [Pg.76]

Dithiolylium-4-olate, 5-methyl-2-phenyl-IR, 6, 818 <76CB740, 78CB2021)... [Pg.20]

Dithiolylium-4-olate, 2,5-diphenyl-reactions with singlet oxygen, 6, 831... [Pg.619]

Diels-Alder reactions, 4, 842 flash vapour phase pyrolysis, 4, 846 reactions with 6-dimethylaminofuKenov, 4, 844 reactions with JV,n-diphenylnitrone, 4, 841 reactions with mesitonitrile oxide, 4, 841 structure, 4, 715, 725 synthesis, 4, 725, 767-769, 930 theoretical methods, 4, 3 tricarbonyl iron complexes, 4, 847 dipole moments, 4, 716 n-directing effect, 4, 44 2,5-disubstituted synthesis, 4, 116-117 from l,3-dithiolylium-4-olates, 6, 826 electrocyclization, 4, 748-750 electron bombardment, 4, 739 electronic deformation, 4, 722-723 electronic structure, 4, 715 electrophilic substitution, 4, 43, 44, 717-719, 751 directing effects, 4, 752-753 fluorescence spectra, 4, 735-736 fluorinated derivatives, 4, 679 H NMR, 4, 731 Friedel-Crafts acylation, 4, 777 with fused six-membered heterocyclic rings, 4, 973-1036 fused small rings structure, 4, 720-721 gas phase UV spectrum, 4, 734 H NMR, 4, 7, 728-731, 939 solvent effects, 4, 730 substituent constants, 4, 731 halo... [Pg.894]


See other pages where Olation is mentioned: [Pg.1214]    [Pg.135]    [Pg.10]    [Pg.10]    [Pg.20]    [Pg.20]    [Pg.20]    [Pg.20]    [Pg.20]    [Pg.36]    [Pg.36]    [Pg.38]    [Pg.38]    [Pg.65]    [Pg.617]    [Pg.619]    [Pg.619]    [Pg.619]    [Pg.619]    [Pg.619]    [Pg.619]    [Pg.718]    [Pg.722]    [Pg.722]    [Pg.723]    [Pg.723]    [Pg.723]    [Pg.825]    [Pg.870]    [Pg.911]    [Pg.34]    [Pg.34]    [Pg.1214]    [Pg.191]    [Pg.908]    [Pg.351]    [Pg.104]    [Pg.160]    [Pg.67]    [Pg.67]    [Pg.67]    [Pg.67]   
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See also in sourсe #XX -- [ Pg.110 ]

See also in sourсe #XX -- [ Pg.168 ]

See also in sourсe #XX -- [ Pg.221 ]

See also in sourсe #XX -- [ Pg.412 ]

See also in sourсe #XX -- [ Pg.8 ]

See also in sourсe #XX -- [ Pg.110 ]

See also in sourсe #XX -- [ Pg.183 , Pg.185 , Pg.193 , Pg.238 , Pg.243 , Pg.247 ]

See also in sourсe #XX -- [ Pg.852 ]




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1.2.3- Benzotriazinium-4-olates

1.2.3- Oxadiazolium-5-olates

1.2.4- Triazolium-3-olates

1.3- Dioxolium-4-olates

1.3- Dithiol-4-olates

1.3- Dithiolium-4-olates

1.3- Dithiolylium-4-olates, cycloaddition reactions

1.3- Oxazinium 4-olates

1.3- Oxazolium-5-olates

1.3- Thiazolium-4-olate

1.3- Thiazolium-4-olates

2- Benzopyrylium-4-olates

2-Benzopyrylium-4-olates cycloaddition

2-Benzothiopyrylium-4-olates

2-Methyl-5-phenyl-dithiolylium-4-olate

2-Methylphthalazin-2-ium-4-olate

2-Phenylphthalazin-2-ium-4-olate

2-Substituted isoquinolinium-olates

2-Substituted isoquinolinium-olates structure

2-benzopyrylium-4-olate

Acridinium-4-olates

Cinnolinium-3-olates

Condensation by olation

From Meso-ionic l,3,2-Oxathiazolium-5-olates

Imidazo thiazolium-3-olate

Imidazolium-4-olat

Indolo isoquinolinium14-olate

Isoquino isoquinolinium-13-olate

Isoquinolinium-4-olate, preparation

Isoquinolinium-4-olates

L,3,2-Oxathiazolium-5-olat

L,3,4-Oxadiazolium-2-olat

L,3-Diazolium-4-olates

L,7-Naphthyridinium-4-olates

L-Methylpyridinium-3-olate

Mesoionic dithiolylium-4-olates

Mesoionic l,3-oxazolium-5-olate

Mesoionic l,3-oxazolium-5-olates

Mesoionic ring systems 1.3- dithiolium-4-olates

Naphthyridinium-4-olates

Olates

Olates

Olation mechanism

Olation reaction

Oxathiazolium olate

Oxatriazolium-5-olates

Phenanthridinium-2-olates

Phthalazinium-1-olates

Pyrazolium-4-olates

Pyridazinium-3-olates

Pyridinium-3-olate

Pyridinium-3-olates

Pyrylium-3-olate

Pyrylium-3-olates

Pyrylium-3-olates generation

Quinolinium-3-olates

Quinolizinium-1-olates

Quinolizinium-l-olates

The Olation Reaction

Thiatriazolium-5-olates

Thiazolium-4-olates cycloaddition

Thiopyrylium-3-olates

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