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Omens

The accuracy of a molecular mechanics or seim-eni pineal quantum mechanics method depends on the database used to parameterize the method. This is true for the type of molecules and the physical and chemical data in the database. Frequently, these methods give the best results for a limited class of molecules or phen omen a. A disad van tage of these methods is that you m u si have parameters available before running a calculation. Developing param eiers is time-consuming. [Pg.21]

Agentu N omen- clature BAN CAS Registry Number Selected trade Empirical formula Refs. [Pg.219]

Agent N omen-clature CAS Registry Selected trade name(s) Empirical formula Refs. [Pg.229]

Horn omen thyl saUcylate (homosalate), employed as a sunscreen agent, is on a Hst of 21 compounds for OTC sunscreen products, recommended by the FDA advisory review panel on OTC bum and sunburn prevention as both "safe and effective" (30). Menthyl saUcylate (6) is also a sunscreen agent. [Pg.290]

Anzeichen, n. sign, indication, symptom, omen, anzeichnen, v.t. mark, indicate, note. [Pg.31]

Vor-wissen, n. foreknowledge, -wort, n. foreword, preface preposition, -wurf, m. subject, object reproach, blame, -zlthlung, /. enumeration, -zeichen, n. indication, symptom, omen Math.) sign, -zeichenwechsel, m. Math.) change d sign. [Pg.498]

It is now well-established that unsymmetrical substituted menthylphosphinates, RR P(0)0Men, as well as the corresponding phosphine-boranes RR P(BH3)OMen and phosphinothioates RR P(S)OMen, can be separated readily into the di-astereomeric forms, and subsequently reacted with Grignard reagents to afford P-chirogenic tertiary phosphines with a high degree of stereospecificity [57]. The... [Pg.12]

We discovered a complementary procedure for conversion of OMen to other functional groups. The ester P-OMen bond was shown to be cleaved in a stereoselective manner reductively [85,86]. The cleavage takes place with almost complete preservation of stereochemical integrity at phosphorus. The reducing agents are usually sodium or Hthium naphthalenide, lithium biphenyUde, and Hthium 4,4 -di-fert-butylbiphenyl (LDBB). The species produced is then quenched with an alkyl hahde or methanol to afford tertiary or secondary phosphines, respectively (Scheme 5b). Overall, the displacement reaction proceeds with retention of configuration. [Pg.13]

In conclusion, the potential of optically active menthylphosphino compounds is vast since the OMen group may be substituted for aryl-, alkyl substituents, or even the H atom. In particular, replacement by a methyl group and H enables one to obtain key intermediates which have been found to be extremely important in the synthesis of other substituted monophosphines or diphosphines, as will be shown in the sections which follow. [Pg.16]

Omen Retention/Rejection During Ether Synthesis Over Resin Catalysts... [Pg.604]

Senyuva, H. Z., Gilbert, J., Silici, S., Charlton, A., Dal, C., Gurel, N., and Omen, D. (2009). Profiling Turkish honeys to determine authenticity using physical and chemical characteristics. /. Agric. Food Chem. 57, 3911-3919. [Pg.133]

Encyclopedia of magic and superstition alchemy, charms, dreams, omens, rituals, talismans, wishes. London Octopus Books, 1974. 5-253 p. ISBN 0-7064-0396-7... [Pg.501]

Nomen est omen. There are no known compounds of the colorless, odorless gas. At 1 %, there is almost 30 times more argon than C02 in the atmosphere. [Pg.127]

A discrete-event simulation tool considers - nomen est omen - discrete events at discrete points in time. Typically, in a discrete-event simulator items such as parts are moving through the modeled system changing their state, e.g., when they enter or leave a machine. A reactor in the process industry continuously produces a certain output. This is something a discrete-event simulator is not really made... [Pg.34]

Misztal (148) prepared 5-methoxy-N-methyltryptamine (5-OMeN-MeT 36) for the purpose of pharmacologic evaluation, but no data were reported. Smythies and co-workers (210) reported that 5-OMeN-MeT was much less active than either DMT or 5-OMeDMT in disrupting the conditioned avoidance response in rats. Taborsky and Mclsaac (229) also found 5-OMeN-MeT to be less active than 5-OMeDMT. These latter authors further demonstrated that 5-OMeN-MeT was rapidly and nearly quantitatively metabolized by MAO to 5-meth-oxyindole acetic acid. Julia and Manoury (123) investigated 5-methoxy and... [Pg.67]


See other pages where Omens is mentioned: [Pg.35]    [Pg.45]    [Pg.389]    [Pg.433]    [Pg.433]    [Pg.1138]    [Pg.67]    [Pg.158]    [Pg.263]    [Pg.12]    [Pg.13]    [Pg.13]    [Pg.13]    [Pg.14]    [Pg.15]    [Pg.492]    [Pg.197]    [Pg.208]    [Pg.208]    [Pg.254]    [Pg.104]    [Pg.67]    [Pg.345]    [Pg.347]    [Pg.349]    [Pg.349]    [Pg.350]    [Pg.352]    [Pg.353]    [Pg.358]    [Pg.359]   
See also in sourсe #XX -- [ Pg.45 ]




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