Big Chemical Encyclopedia

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

Articles Figures Tables About

Ring forming

As carbazoles, where a ring containing nitrogen is condensed with one or more aromatic rings, forming neutral compounds. [Pg.12]

Ring forming reaction is designated as Favored or Disfavored... [Pg.136]

Ph.CH2.OMe, Ph.(CH2)2.0Me, Ph.(CH2)3.0Me (2-3, 3-4, 1-3), does not decrease steadily, but goes through a maximum. These two circumstances point to a specific -interaction in nitrations of the ethers with acetyl nitrate which is important with benzyl methyl ether, more important with methyl phenethyl ether, and not important with methyl phenpropyl ether. This interaction is the reaction with dinitrogen pentoxide already mentioned, and the variation in its importance is thought to be due to the different sizes of the rings formed in the transition states from the different ethers. [Pg.102]

Hemiacetal formation between the carbonyl group and the C 4 hydroxyl yields the five membered furanose ring form The anomenc carbon is a new chirality center its hydroxyl group can be either cis or trans to the other hydroxyl groups of the molecule... [Pg.1033]

Cyclodienes. These are polychlorinated cycHc hydrocarbons with endomethylene-bridged stmctures, prepared by the Diels-Alder diene reaction. The development of these insecticides resulted from the discovery in 1945 of chlordane, the chlorinated adduct of hexachlorocyclopentadiene and cyclopentadiene (qv). The addition of two Cl atoms across the double bond of the ftve-membered ring forms the two isomers of chlordane [12789-03-6] or l,2,4,5,6,7,8,8-octachloro-2,3,3t ,4,7,7t -hexahydro-4,7-methano-lJT-indene, QL-trans (mp 106.5°C) and pt-tis (32) (mp 104.5°C). The p-isomerhas signiftcantiy greater insecticidal activity. Technical chlordane is an amber Hquid (bp 175°C/267 Pa, vp 1.3 mPa at 25°C) which is soluble in water to about 9 fig/L. It has rat LD qS of 335, 430 (oral) and 840, 690 (dermal) mg/kg. Technical chlordane contains about 60% of the isomers and 10—20% of heptachlor. It has been used extensively as a soil insecticide for termite control and as a household insecticide. [Pg.277]

Fig. 2. Conversion from open-chain to ring forms of aldosugars. When ring closure occurs, a new chiral center is formed and two C-1 configurational... Fig. 2. Conversion from open-chain to ring forms of aldosugars. When ring closure occurs, a new chiral center is formed and two C-1 configurational...
Fig. 3. Equilibiium mistuie of D-glucose forms in solution. Pyranose ring forms predominate. Fig. 3. Equilibiium mistuie of D-glucose forms in solution. Pyranose ring forms predominate.
The stmcture of monosaccharides is often written in the acycHc form although only very minor amounts of it ever occur in that form. Because the interconversions are rapid, the carbonyl groups of sugars can and do react both as if they are free and as if they are in a hemiacetal ring form. [Pg.475]

The 1,2,4-trioxolane ring prefers a half-chair conformation (131) the C—O—C portion of the ring forms the reference plane, and alkyl substituents prefer the equatorial positions. [Pg.35]

New materials - As soon as a new elastomer eompound is developed, it beeomes available and produced in the o-ring form. Examples are Kalraz , and Zalak produced by Dupont, Aflas produced by 3M, and Parafluor by Parker Hannifin. [Pg.188]

These layouts are configured as shown in Figure 6-25. The cantilevered support ribs, along with die sector diey are supporting at bodi ends, form a centering spring element. The small gap between die sector and die outer ring forms die squeeze film damper clearance... [Pg.364]

There have been several representations of the bonding in benzyne. The one most generally used pictures benzyne as being similar to benzene but with an additional weak bond in the plane of the ring, formed by overlap of the two sp orbitals. Comparison of the NMR characteristies with MO ealeulations indieate that the eonjugation is maintained and that benzyne is a strained but aromatie moleeule. ... [Pg.594]

One of the prime tenets of the template effect is that a cation of appropriate size coordinates with the heteroatom binding sites in the incipient ring system. Evidence to be discussed below indicates that there is a clear relationship between the size of the coordinating cation and the size of the ring formed. Before presenting this evidence, it is useful to note the approximate ring sizes of common crowns and the known ionic diameters of sundry metal cations. This is done in Table 2.1. [Pg.13]

An unusual seven-membered ring-forming rearrangement was observed m the addition of diazomethane to a perfluorinated cyclobutene [5] (equation 3)... [Pg.798]

There are several other far less common types of helices found in proteins. The most common of these is the Sjq helix, which contains 3.0 residues per turn (with 10 atoms in the ring formed by making the hydrogen bond three residues up the chain). It normally extends over shorter stretches of sequence than the a-helix. Other helical structures include the 27 ribbon and the 77-helix, which has 4.4 residues and 16 atoms per turn and is thus called the 4.4ig helix. [Pg.168]

The special properties of lipoic acid arise from the ring strain experienced by oxidized lipoic acid. The closed ring form is approximately 20 kj higher in energy than the open-chain form, and this results in a strong negative reduction potential of about —0.30 V. The oxidized form readily oxidizes cyanides to isothiocyanates and sulfhydryl groups to mixed disulfides. [Pg.601]

In addition to ring-forming reactions, the transformation of preformed heterocycles serves as an efficient alternative route for the synthesis of... [Pg.125]

The 0x0 formulations 143 and 144 (X, Y, Z N or CH) are supported for this type of compound by infrared and ultraviolet spectral data. With certain substituents in the five-membered ring, forms of type 145 apparently become important/ and structure 146 is postulated to predominate on the basis of ultraviolet evidence. Com-... [Pg.59]


See other pages where Ring forming is mentioned: [Pg.333]    [Pg.135]    [Pg.325]    [Pg.74]    [Pg.891]    [Pg.398]    [Pg.121]    [Pg.406]    [Pg.469]    [Pg.256]    [Pg.190]    [Pg.474]    [Pg.475]    [Pg.475]    [Pg.475]    [Pg.479]    [Pg.382]    [Pg.386]    [Pg.244]    [Pg.539]    [Pg.90]    [Pg.470]    [Pg.81]    [Pg.171]    [Pg.891]    [Pg.94]    [Pg.330]    [Pg.616]    [Pg.350]    [Pg.1278]    [Pg.189]    [Pg.419]   
See also in sourсe #XX -- [ Pg.324 ]




SEARCH



A Cycloaddition Forming Three-Membered Rings

Amadori, products ring form

Bidentate Ligands Forming Four-Membered Rings with Silicon

Bronsted ring-forming reactions

Carbenes ring-forming reactions

Diels ring-forming

Enamine ring-forming reactions

Five-and Six-Membered Ring Forms

Glucose ring form

Hetero ring-forming

Hydrogen ring-forming reactions

Iminium ring-forming reactions

Indoles ring-forming

Intramolecular ring-forming reaction

Kekule forms aromatic rings

Miscellaneous Nucleophilic Cyclizations that Form the Indole Ring

N Ring-Forming Reactions by Transition Metal-Catalyzed

N ring-forming reactions

Other Ring-Forming Reactions

Pyrazines ring transformations forming

Radical cyclization forming furan rings

Reactions to form six-membered rings

Resolution Ring-forming reactions

Ribose ring form

Ring conversions, forming thiophenes

Ring forming process

Ring forming step

Ring transformations forming pyridazines

Ring-forming functionalities

Ring-forming reactions

Ring-forming reactions Tributyltin hydride

Ring-forming reactions chelate

Ring-forming reactions rings

Ring-forming reactions, general

Ring-forming strategies

Ring-forming transforms

Rings Formed by Hydrogen Bonding

Rings, intramolecularly formed

Robinson ring-forming reaction

Strengths of the Bonds Formed between Free Radicals and Aromatic Rings

Syntheses from the Pre-formed Thiazole Ring

To form Five-Membered Rings

Transform ring-forming

© 2024 chempedia.info