Indanyl

Chemical Name N-(2-carboxy-3,3-dimethvl-7-oxo-4-thia-1-azabicyclo[3.2.0I hept-6-yl)-2-phenylmalonamic acid, 1-(5-indanyl ester), monosodium salt... 

B) Acylation of 6-Aminopenicillanic Acid To a solution of the aryl halocarbonyl ketene (0.1 mol) in methylene chloride (sufficient to provide a clear solution and generally from about 5 to 10 ml per gram of ketene) there is added the proper alcohol RjOH (0.1 mol), in this case 5-indanyl alcohol. The reaction mixture is maintained under an atmosphere of nitrogen and stirred for a period of from 20 minutes to 3 hours, care being taken to exclude moisture. The temperature may range from about -70° to about -20°C. The infrared spectrum of the mixture is then taken to determine and confirm the presence of the ketene ester. A solution of 6-aminopenicillanic acid-triethylamine salt (0.1 mol) in methylene chloride (50 ml) is added and the mixture stirred at -70° to -20°C for 10 minutes. The cooling bath is then removed and the reaction mixture stirred continuously and allowed to warm to room temperature. 

Ghosh and co-workers have recently used the indanyl-derived auxiliary 69 (Table 1.9) in titanium enolate condensations with a range of aldehydes [34], Of the four possible diastereomers, only the anti 71 and syn TL were produced (the alternative anti and syn diastereomers were not detected by 1H or 13C NMR). The use of monodentate aliphatic aldehydes resulted in the formation of anti diastereomers... 

GjHuO 40731-98-4) see Indeloxacine A -[2(R)-bydroxy-l(5)-indanyl]-3-phenylpropanamide (CijHiijNOj 142479-00-3) see Indinavir sulfate 4-bydroxyindene... 

Of a series of indanylthiocarbamates, to1 indate (2) had significant antifungal properties. It is prepared simply from 5-indanyl thionochloroformate (1) by reaction with N-methyl-m-toluidine. It presumably joins the fairly large family of organic compounds having sulfur divalently bound to carbon which are useful topical agents for dermatophytes. 

In the polystyrenes produced by cationic initiators most of the chain-ends are terminal indanyl groups, and olefinic groups are rare. As this terminal indanyl group cannot be aluminated like a double bond, the amount of tritium incorporated comes only from the initial AlBr2CH2CHPh-groups and the few residual terminal double bonds and it, therefore, represents (approximately) the total number of initiated chains. 

There is general agreement that stages I and III are truly ionic reactions which are not due to the very abundant, colour-conferring indanyl ions, but to a very small concentration... 

Oligostyrene with +HA Allylic indanyl end-groups lons... 

This absorption is in fact due to the ions derived from l-methyl-3-phenylindane (the cyclic dimer of styrene) and its higher homologues (oligostyrenes with indanyl end groups). There can be no doubt that the ions formed at the end of the polymerisation of styrene belong to the same families of compounds (indanyl and various phenyl alkyl carbonium ions [7]). Our evidence showed that the 1-phenylethyl cation is absent from the ions formed from styrene by excess of acid its dimeric homologue, the l,3-diphenyl- -butyl cation, is a minor component of the ion mixture. We refer to this mixture of ions formed rapidly from styrene by excess acid, or at the end of a styrene polymerisation, as SD (styrene-derived) ions. 

If the reaction mixture was left under vacuum for several hours after the end of the ionogenic reaction described in Section 3, the polymer no longer contained double-bonds (UV spectrum), indicating that the formation of indanyl end-groups went to completion. At the same time D424 fell to zero and the conductivity decreased to the background level due to impurities. 

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