Derivatives substituted groups

In a similar reaction the bis-tosylate shown below was to be converted into a bis-malonate derivative. In this cyclic derivative both groups are hold closely together and intramolecular reactions proved to be so much faster than intermolecular substitution under all ex-... 

Substituted derivatives of groups (1) and (2) above, e.g. 3-methylcyclo-butene and 1-methylcyclo-octa-l,5-diene. 

The term primary radical used in this context should be distinguished from that used when describing the substitution pattern of alkyl radicals, t For example, in PS the initiator-derived end groups will account for ca 0.2% of units in a sample of molecular weight 100,000 (termination is mainly by combination). 

Nitriles are organic derivatives of hydrocyanic acid in which the substituting group is attached to carbon. Their formula is R.C N. Because most nitriles can be derived from corresponding acid amides, R.CO.NH2, by removal of w, they are called nitriles. For instance, the compd CH3.CN is called acetonitrile because it is derived from acetamide. It can also be called methyl cyanide. The compd C2HS.CN is called either propionitrile or ethyl cyanide, etc The first nitrile to be prepared was propionitrile which J. Pelouze obtained in 1834 by distg Ba ethyl sulfate with K cyanide... 

The second extrathermodynamic method that we discuss here differs from Hansch analysis by the fact that it does not involve experimentally derived substitution constants (such as o, log P, MR, etc.). The method was originally developed by Free and Wilson [29] and has been simplified by Fujita and Ban [30]. The subject has been extensively reviewed by Martin [7] and by Kubinyi [8]. The method is also called the de novo approach, as it is derived from first principles rather than from empirical observations. The underlying idea of Free-Wilson analysis is that a particular substituent group at a specific substitution site on the molecule contributes a fixed amount to the biological activity (log 1/C). This can be formulated in the form of the linear relationship ... 

Reduced indicator table and bacteriostatic activities 1/Z of 10 triply substituted tetracyclines, as derived from Table 37.3. The compound with substitution groups H, NO2 and NO2 at the positions U, V and W is taken as the reference compound. 

Several zinc(II) and aluminum(III) phthalocyanine derivatives substituted with carboxylic acid and sulfonic acid groups were anchored to nanocrystalline Ti02 films and tested for their photovoltaic behavior.72,73 Interestingly, zinc(II)-2,9,16,23-tetracarboxyphthalocyanine (55) exhibited 45% monochromatic current conversion efficiency at 700 nm. It is shown that electron injection to Ti02 occurs from the excited singlet state of the phthalocyanine derivatives. The... 

Other -substituted and reduced 2-azepinone derivatives 22 can also be accessed in high yields (Table 3) by ring closing metathesis on the precursors 21 using Grubbs II catalyst 18. A variety of IV-heteroaryl substitutent groups were tolerated in this reaction <06TL3295>. 

Preparation of benzotriazolyl derivatives substituted at N-l (or N-2) with variety of functional groups is described in detail in Sections 5.01.5 and 5.01.8. The basic strategy starts from a reaction of benzotriazole with an electrophile. In most cases, the reaction produces a mixture of benzotriazol-l-yl and benzotriazol-2-yl derivatives that is not difficult to separate. Further modification of the substituent in subsequent steps leads to the desired product. 

Keto Derivatives of Group IV Organometalloids, 7, 95 Lewis Base-Metal Carbonyl Complexes, 3, 181 Ligand Substitution in Transition Metal ir-Complexes, 10, 347 Literature of Organo-Transition Metal Chemistry 1950-1970, 10, 273 Literature of Organo-Transition Metal Chemistry 1971,11, 447 Literature of Organo-Transition Metal Chemistry 1972, 12, 379 Mass Spectra of Metallocenes and Related Compounds, 8, 211 Mass Spectra of Organometallic Compounds, 6, 273... 

A chiral bis(oxazolinyl)phenylrhodium complex was found to catalyze the asymmetric hydrosilylation of styrenes with hydro(alkoxy)silanes such as HSiMe(OEt)2 (Scheme 7).47 Although the regioselectivity in forming branched product 27 is modest, the enantiomeric purity of the branched product 27 is excellent for styrene and its derivatives substituted on the phenyl group. The hydrosilylation products were readily converted into the corresponding benzylic alcohols 29 (up to 95% ee) by the Tamao oxidation. 

For the addition of ethylene, EtOAc as solvent was particularly advantageous and gave 418 in 60% yield (Scheme 6.86). The monosubstituted ethylenes 1-hexene, vinylcyclohexane, allyltrimethylsilane, allyl alcohol, ethyl vinyl ether, vinyl acetate and N-vinyl-2-pyrrolidone furnished [2 + 2]-cycloadducts of the type 419 in yields of 54—100%. Mixtures of [2 + 2]-cycloadducts of the types 419 and 420 were formed with vinylcyclopropane, styrene and derivatives substituted at the phenyl group, acrylonitrile, methyl acrylate and phenyl vinyl thioether (yields of 56-76%), in which the diastereomers 419 predominated up to a ratio of 2.5 1 except in the case of the styrenes, where this ratio was 1 1. The Hammett p value for the addition of the styrenes to 417 turned out to be -0.54, suggesting that there is little charge separation in the transition state [155]. In the case of 6, the p value was determined as +0.79 (see Section 6.3.1) and indicates a slight polarization in the opposite direction. This astounding variety of substrates for 417 is contrasted by only a few monosubstituted ethylenes whose addition products with 417 could not be observed or were formed in only small amounts phenyl vinyl ether, vinyl bromide, (perfluorobutyl)-ethylene, phenyl vinyl sulfoxide and sulfone, methyl vinyl ketone and the vinylpyri-dines. 

The assignment of the monomer solution spectrum was performed by using an NMR spectral database system (SDBS-NMR)54. The signals of the six acetylene carbons from 60.34 to 81.91 ppm in the solution spectrum indicated the monomer structure of a dodec-ahexyne derivative substituted symmetrically by alkyl groups. Since the spectral patterns in Figure 36A are almost the same as those of the monomer, only a small extent of polymerization had occurred during the 30 min after recrystallization. The signal at about... 

Substitution at the 9-position was well tolerated, but some long-chain lipophilic substituents or acyl groups reduced activity. Alkylation or acylation of the unsubstituted compound in the presence of sodium hydride afforded derivatives substituted on the indole nitrogen atom (Table 7.4). 

Psilocybin (Figure 3.5a) and psilocin (Figure 3.5b) are indole derivatives substituted in position 4 by a hydroxyl group, where psilocybin is phosphory-lated. Due to its ionic properties, psilocybin is soluble in water. In addition, phosphorylation protects psilocybin from oxidative degradation. Both compounds are found to affect laboratory animals, but there is evidence that only the dephosphorylated form, psilocin, is the active species. In their structure the toxins resemble serotonine, a biogenic amine known to be a neurotransmitter. 

Preparation of cyclodextrin derivatives substitution at a secondary hydroxyl group of the cyclodextrin annulus. Murakami and cowor-kers described a new and convenient method for the regioselective tosylation of the 2-hydroxyl groups of alpha, beta, and gamma cyclodextrin by means of a cyclic tin intermediate. The method is based on the reaction of dibutyltin oxide with 1,2-diols to form five-membered dibutyl-stannylidene derivatives. Useful yields of the 2-6>-tosyl derivatives of the cyclodextrins were obtained. 

---