Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cross conjugation

Conjugated, cross-conjugated, and homoconjugated fluoroalkenes react with halogens to yield predominantly 1,4-adducts Results from the reactions of a series of conjugated fluoroalkenes with elemental halogens are summarized in Table 4 In nearly all cases, the fraMs-l,4-addition products are formed exclusively [Il ... [Pg.367]

The literature of diene and polyene photochemistry provides many cases of synthetically useful reactions. As a result, certain arbitrary decisions have been made regarding what is covered in this chapter. For example, intramolecular [2 + 2]-photocycloaddition reactions of a, >-dienes can be formally included under the general rubric of diene photochemistry. However, we have chosen to restrict our discussion to dienes and polyenes which constitute a self-contained chromophore, viz. conjugated, cross-conjugated and 1,4-diene systems. Likewise, arene-olefin photocycloadditions will not be considered. These two broad classes of photoreactions have been applied extensively in synthesis, and have been the subject of recent reviews3,4. [Pg.264]

Figure 7.12 Chemical structure of a linear poly(p-phenylene ethynylene) (PPE) and the ligand exchange process utilized hy Kokil et al. (2003) to yield a conjugated cross-linked MSP network and gel. Figure 7.12 Chemical structure of a linear poly(p-phenylene ethynylene) (PPE) and the ligand exchange process utilized hy Kokil et al. (2003) to yield a conjugated cross-linked MSP network and gel.
A competitive enzyme immunoassay for the quantification of ivermectin residues in bovine liver has also been reported recently (85). This method uses a polyclonal antiserum raised in rabbits against 5-O-succinoylivermectin-trans-ferrin conjugate. Cross-reactivity was demonstrated with doramectin, a member... [Pg.849]

Friden, P.M., et al. 1991. Anti-transferrin receptor antibody and antibody-drug conjugates cross the blood-brain barrier. Proc Natl Acad Sci USA 88 4771. [Pg.609]

P. M. Friden, L. P. Wahis, G, F. Musset M. A. Bylor, B. Malfroy, and R. M. Statzyk. Anti-transferrin ieoeptra antibody and antibody-drug conjugates cross the blood brain harrier. Proc NatL Acad. ScL UU 68 4771-4775 (1991). [Pg.36]

When perflluoro(2-methylpropene) reacts with tributylphosphane in acetonitrile at — 30"C, the reaction does not stop with the formation of fluoro-2 -phosphanes, and, as a result of a series of transformations, perfluorodiene 3 and conjugated cross-triene 4 are formed. When the reaction is carried out with triphenylphosphane in acetonitrile without cooling triene 4 is obtained in 67 % yield.On the other hand, the reaction of perfluoro(2-methylpropcnc) with tributylphosphane in diethyl ether at — 70 C leads to the corresponding fluoro-A -phos-phane treating this compound with potassium fluoride dihydrate in tetraglyme gives 1,1,1,3-tetrafluoro-2-(trifluoromethyl)hept-3-ene in 75% yield,... [Pg.431]

Hinds, K.D., Protein conjugation, cross-linking, and PEGylation, in Biomaterials for Delivery and Targeting of Proteins and Nucleic Acids, Mahato, R.I., Ed. CRC Press LLC, Boca Raton, Fla, 2005, 119-185. [Pg.400]

Conjugated, cross-conjugated, and pseudo cross-conjugated mesomeric betaines have been defined <85T2239>. It is evident from the definition, that mesomeric heteropentalene (7) and its... [Pg.765]

Zotti, G., R. Salmaso, M.C. Gallazzi, and R.A. Marin. 1997. In situ conductivity of a polythiophene from a branched alkoxy-substituted tetrathiophene. Enhancement of conductivity by conjugated cross-linking of polymers chains. Chem Mater 9 791-795. [Pg.538]

Reaction of a malondialdehyde (MDA) carbonyl group with amino groups leads to the formation of imines, but formation of these structures is of no nutritional concern, because they are hydrolysed at the acidic pH of the stomach. AT-Prop-2-enals, which are absorbed from the gut, are also formed in neutral or acidic aqueous media, but most of the absorbed material is not metaboHsed. A third type of reaction products are unavailable 4-substituted l,4-dihydropyridine-3,5-dicarbaldehydes, which arise in reactions of malondialdehyde with amino compounds, such as lysine, in the presence of alkanals. Examples of malondialdehyde reaction products with lysine are lV -(prop-2-enal)lysine, so-called MDA-lysine, JV -(prop-2-enal)lysine, ArAf -di(prop-2-enal)lysine (3-150) and conjugated cross-hnk in proteins termed lysine-MDA-lysine. An example of the reaction product of lysine with malondialdehyde and acetaldehyde is Ar,Ar-di(4-methyl-l,4-dihydropyridine-3,5-dicarbaldehyde)lysine, which, for example, arises in the reaction of bovine serum albumin with malondialdehyde and acetaldehyde (3-151). [Pg.195]

Cross-conjugated s. Dienones, cross-conjugated Cross-coupling with Grignard compds. 26,875... [Pg.248]

The second thematic section of the volume will cover some questions from the more theoretical side. In particular, we willbeconcernedwiththe (eventual) use of cross-conjugated systems in material science. Compared to linear conjugation, cross-conjugation leads to very different chemical and physical properties, and these should have a strong influence on, for example, the photophysical properties of the respective compounds. [Pg.478]

Steroid conjugates cross the placental barrier more slowly than free steroids. [Pg.216]


See other pages where Cross conjugation is mentioned: [Pg.312]    [Pg.192]    [Pg.225]    [Pg.229]    [Pg.49]    [Pg.176]    [Pg.355]    [Pg.55]    [Pg.575]    [Pg.310]    [Pg.223]    [Pg.498]    [Pg.849]    [Pg.40]    [Pg.268]    [Pg.244]    [Pg.264]    [Pg.271]    [Pg.225]    [Pg.229]   
See also in sourсe #XX -- [ Pg.39 ]

See also in sourсe #XX -- [ Pg.179 , Pg.181 ]




SEARCH



Acetylene-extended cross-conjugated systems

Allenyne cross-conjugated trienes

Antibody-enzyme conjugation cross-linkers

Antibody-toxin conjugates cross-linkers

Antibody—toxin conjugates disulfide cross-linkers

Aprotic solvents, cross-conjugated

Betaines cross-conjugated

Conjugate addition cross-coupling reactions

Conjugation linear and cross

Conjugation using cross-linkers

Cross Conjugation: Dendralene, Radialene and Fulvene Chemistry, First Edition

Cross-Conjugated Systems in Acetylene-Extended Radiaannulene Frameworks

Cross-Conjugated Triene Formation

Cross-Conjugation and Electronic Structure in TTF Analogs

Cross-Conjugation and Quantum Interference

Cross-Conjugation in Expanded Systems

Cross-Conjugation in Synthesis

Cross-bridge conjugates

Cross-conjugated

Cross-conjugated

Cross-conjugated compounds, palladium

Cross-conjugated copolymers

Cross-conjugated cyclic dienones

Cross-conjugated cyclohexadienones

Cross-conjugated cyclohexadienones photochemical

Cross-conjugated cyclohexadienones rearrangements

Cross-conjugated dianions

Cross-conjugated diene

Cross-conjugated dienone

Cross-conjugated dienones

Cross-conjugated dienyltricarbonyliron cations

Cross-conjugated enediynes

Cross-conjugated enolate

Cross-conjugated mesomeric betaines

Cross-conjugated polyene

Cross-conjugated s. Dienones

Cross-conjugated trienes

Cross-conjugated trienes, formation

Cross-coupling reactions 1-alkenylboron. conjugated diene synthesis

Cross-coupling reactions conjugated diene synthesis

Cross-coupling reactions polymer conjugation

Cyclic cross-conjugated

Cyclic cross-conjugated systems

Dienes cross-conjugated—

Enynes, conjugated cross-benzannulation with diynes

Expanded cross-conjugated systems

Hapten-carrier conjugation cross-linkers

Polyenes cross-conjugated—

Preparation of Immunotoxin Conjugates via Amine- and Sulfhydryl-Reactive Heterobifunctional Cross-linkers

Pseudo-cross-conjugated heterocyclic

Pseudo-cross-conjugated heterocyclic mesomeric betaines

Rearrangements of cross-conjugated cyclohexadienones and their photoisomers

Silyl dienol ethers cross-conjugated

TTFs in Cross-Conjugated Systems

Tamio Hayashi 17 Synthesis of Conjugated Oligomers and Polymers via Palladium-Catalyzed Cross-Coupling

The Nazarov Cyclization of Cross-Conjugated Ketones

The Transport Properties of Cross-Conjugated Molecules

Wavelengths cross-conjugated

© 2024 chempedia.info