Hetero-Linked

One interesting difference between the known examples of 2H- and 4H-imidazoles is that nearly all in the latter group contain at least one hetero-linked substituent. This arises because the major synthetic approach is via imidazolone derivatives (see next section) a second important route using 1,2-diketones places an OH group at C-4, and electrophilic additions to 1//-imidazoles also tend to introduce heteroatoms at this site. 

Hetero-Linked Auxiliaries Chiral Vinyl Ethers... 

P. which contain only amino acid residues are called homomeric P., whereas P. with non-amino acid constituents are known as heteromeric P. Each of these classes is further subdivided into homodetic P., which contain only peptide bonds, and heterodetic P, which contain other bonds, e.g. ester, thioether or disulfide. Heterodetic P. possessing one or more ester bonds as hetero link are called Depsipeptides (see). The classification of depsipeptides does not accord entirely with the homomeric/heteromeric system it has arisen from the fact that the synthesis of these peptides presents rather special problems. There are two types of homomeric depsipeptides O-peptides contain ester-linked hydroxyamino acids, and they may be linear or cyclic (i. e. lactones) in S-peptides or thiodepsipep-tides, the mercapto group of a cysteine residue is acy-lated with an amino acid. Heteromeric depsipeptides contain hydroxy acids as the hetero component, and they are also known as peptolides. P. with non-amino... 

Dialkyl peroxides have the stmctural formula R—OO—R/ where R and R are the same or different primary, secondary, or tertiary alkyl, cycloalkyl, and aralkyl hydrocarbon or hetero-substituted hydrocarbon radicals. Organomineral peroxides have the formulas R Q(OOR) and R QOOQR, where at least one of the peroxygens is bonded directly to the organo-substituted metal or metalloid, Q. Dialkyl peroxides include cyclic and bicycflc peroxides where the R and R groups are linked, eg, endoperoxides and derivatives of 1,2-dioxane. Also included are polymeric peroxides, which usually are called poly(alkylene peroxides) or alkylene—oxygen copolymers, and poly(organomineral peroxides) (44), where Q = As or Sb. 

Whereas the fulvalenes 1-6 are relatively unstable hydrocarbons and therefore largely of theoretical interest, their heteroatom analogs demand considerable attention in synthetic chemistry and material sciences. Tlie general principle of heterocyclic chemistry to relate heterocyclic compounds to carbocyclic ones was the driving force for the synthesis and their application to heteroful-valenes. Numerous heterocyclic derivatives iso-rr-electronic with, for example, heptafulvalene 3 were accessible in which pairs of carbon atoms linked by double bonds were replaced by heteroatoms capable of contributing two tt-electrons. By this principle, the well-known tetrathiafulvalene and its derivatives have been synthesized successfully (Scheme 2). 

The spiro dimer of a-tocopherol (9, see also Fig. 6.4) is formed as mixture of two diastereomers by dimerization of the o-QM 3 in a hetero-Diels-Alder reaction with inverse electron demand. Both isomers are linked by a fluxion process (Fig. 6.22), which was proven by NMR spectroscopy.53 The detailed mechanism of the interconversion, which is catalyzed by acids, was proposed to be either stepwise or concerted.53-55... 

The synthesis of multivalent neoglycoconjugates by 1,3-dipolar cycloaddition of nitrile oxides and alkynes has been reported (493). The nitrile oxides have been generated in situ in the presence of alkynyl derivatives, allowing the access to homo and hetero multivalent systems containig O- and C-linked glycosides and isoxazole bridges. 

These are prepared from a polyacrylamide (which may be cationic) and glyoxal (Figure 7.30). The glyoxylated polyacrylamide may then participate in homo- or hetero-cross-linking (Figures 7.31 and 7.32). 

Although no En cluster molecules with n > 4 are known in the condensed phase, it has been shown [27] that neutral P6 can be generated in the gas phase by neutralization-reionization mass spectrometry with cp 2 6 as a precursor [cp = C5(CH3)5] [28]. Since the cp 2P6 precursor molecule already has a hetero-benzvalene P6 skeleton, it was inferred that the neutral P6 molecule should have the benzvalene structure as shown in Figure 2.6-5. This is in agreement with a multitude of quantum chemical calculations [8, 11, 27, 29-32]. Note that the handle of the basket of P6 includes two dicoordinate P atoms linked by a P=P double bond (cf. R-P=P-R 203 pm [33]). 

Similar intramolecular cycloadditions are encountered where an ether linkage has been incorporated into the met a or para linking groups 123. In these cyclizations the better yields were obtained from the para-attached systems. The yields obtained are again dependent on the chain length of the separator and are indicated below the appropriate structures (124)57. Other hetero-atom-substituted cyclophanes (125) can be obtained by irradiation of the divinyl compounds (126)58,59. The use of tin and germanium derivatives... 

The l homo/ hetero was also estimated by B/E linked scanning of FAB-MS." ... 

The hetero-l,4-linked xylans (or heteroxylans) constitute a well-characterized group of polysaccharides which form the major components of the hemicellulosic fractions of terrestrial plants (1-4). Softwoods are an exception, where the heteroxylans can be present as a minor component of the total hemicelluloses. They have been isolated from grasses, legumes, ferns, softwoods and hardwoods, and collectively may constitute up to 35% of the total dry weight of higher land plants (4). As such the heteroxylans rank second to cellulose in abundance as naturally occurring organic chemicals in the biosphere. The heteroxylans are closely associated with other... 

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