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Saturated ring compounds

Indicator variable for which the value is 1 for saturated ring compounds otherwise the value is zero Indicator variable for which the value is 1 for compounds with substituents at the 5- or 6- position of 2-nitronaphtofur-ans and pyrenofurans otherwise the value is zero Molecular refractivity, which is a measure of the substituent bulk for any substituents that are next to the nitro group, negative coefficient indicates its detrimental effect toward log SOSIP... [Pg.235]

This phenomenon also occurs in saturated ring compounds having three or more members in the ring, as well as in certain coordination compounds. [Pg.602]

Significant amounts of partially or fully saturated ring compounds were found in the jet and diesel products. Mono- and dicyclic alkanes were a major portion of the saturate fraction... [Pg.244]

The coordinately saturated rings have weaker B—N bonding, as evidenced by the oligomerization equilibria ( 15.2.5.1.2) and by interconversion reactions ( 15.2.5.4). Inasmuch as the substituent groups dominate the nature of stability, however, saturated ring compounds may have greater thermal and/or hydrolytic stability than the borazines (HNBH)j decomposes slowly at RT, whereas (HjNBHjjs is stable up to 150°C. [Pg.154]

The coordinately saturated ring compounds owe their stabilities to both additional steric effects and the unavailability of sites for electrophilic or nucleophilic attack. A clear discrimination between the relative influence of these factors is often difficult, but the fact that (H2NBH2)3 is unaffected by boiling water while (HNBHjj is rapidly hydrolyzed must be largely a consequence of the latter. [Pg.156]

Pyrrolidine is the saturated ring compound corresponding to pyrrole. [Pg.46]

Coke-oven tar is an extremely complex mixture, the main components of which are aromatic hydrocarbons ranging from the monocyclics benzene and alkylbenzenes to polycycHc compounds containing as many as twenty or more rings. HeterocycHc compounds containing oxygen, nitrogen, and sulfur, but usually only one heteroatom per ring system are present. Small amounts of paraffinic, olefinic, and partly saturated aromatic compounds also occur. [Pg.343]

A saturated ring with an aliphatic side chain favors cleavage at the bond connecting the ring to the rest of the molecule. Compounds containing cyclohexyl rings fragment at m/z 83, 82, and 81, corre-... [Pg.85]

The disilanickela complex 21 is an effective catalyst for the double silylation of some alkenes. Thus, reaction of 11 with 2 equiv. of4-vinylanisole in the presence of a catalytic amount of 21 afforded a moderate yield of the five-membered disilylene compound 30. However, treatment of 11 with 1.2 equiv. of 1,1-diphenylethylene in the presence of a catalytic amount of 21 gave five-membered disilylene ring compound 31, which contained a saturated side chain. [Pg.68]

Shown below are the aromatic ring systems and names of compounds in this book used for Method 1. There are two types of these. The ori/zo-fused and the ortho- and peri-fused rings. For each of the ori/zo-fused ring systems the corresponding saturated ring system and the name obtained by Method 2 is shown. [Pg.22]

Ring Syntheses of Saturated Rings from Acyclic Compounds 430... [Pg.409]


See other pages where Saturated ring compounds is mentioned: [Pg.111]    [Pg.554]    [Pg.186]    [Pg.2536]    [Pg.39]    [Pg.77]    [Pg.9]    [Pg.996]    [Pg.418]    [Pg.333]    [Pg.491]    [Pg.111]    [Pg.554]    [Pg.186]    [Pg.2536]    [Pg.39]    [Pg.77]    [Pg.9]    [Pg.996]    [Pg.418]    [Pg.333]    [Pg.491]    [Pg.158]    [Pg.158]    [Pg.172]    [Pg.81]    [Pg.126]    [Pg.49]    [Pg.3]    [Pg.290]    [Pg.111]    [Pg.123]    [Pg.689]    [Pg.92]    [Pg.207]    [Pg.82]    [Pg.405]    [Pg.54]    [Pg.120]    [Pg.175]   


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Ring saturation

Saturated compounds

Saturated rings

Saturation compound

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