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Additive synthesis

Additive synthesis is deeply rooted in the theory of Fourier analysis. The technique assumes that any periodic waveform can be modelled as a sum of sinusoids at various amplitude envelopes and time-varying frequencies. An additive synthesiser hence functions by [Pg.50]

Although additive synthesis specifically refers to the addition of sinusoids, the idea of adding simple sounds to form complex timbres dates back to the time when people started to build pipe organs. Each pipe produced relatively simple sounds that combined to form rich spectra. In a way, it is true to say that the organ is the precursor of the synthesiser. [Pg.51]


Earlier reported syntheses have been shown to give isoxazolin-5-ones. Other isoxazolin-3-ones have been prepared by the reaction of methylacetoacetic esters and hydroxylamine. An additional synthesis was reported by the action at 0°C of hydroxylamine on ethyl -benzoylpropionate to produce an insoluble hydroxamic acid which cyclized on acid treatment. The hydroxamic acid acetal was similarly transformed into the isoxazolin-3-one (Scheme 149) (71BSF3664, 70BSF1978). [Pg.106]

In addition, synthesis of reference compounds and a comparison of HPLC retention characteristics and mass spectral data is often reqnired. [Pg.268]

Subsequent to the initial report by Badley et al. two communications appeared, which reported structural investigations on several products obtained from PtCl4 , methyl isocyanide, and hydrazine 33, 117) these compounds had previously been identified (incorrectly) as six-coordinate platinum(II) species 90). In addition, synthesis work in this area was extended somewhat further by these groups. The details of this work presented in these communications and in later full papers 34, 117) are summarized hy Eqs. (17). [Pg.43]

When compared with other monoamines, HA levels are low, with the highest levels seen in the hypothalamus and the lowest in the cerebellum. In addition, synthesis and release of HA is under circadian control. In rats, the average HA... [Pg.146]

Ring olosure of hydroxyalkylsulfonyl ohiorldes Reaotlon of cumulative and conjugated double bonds and SO3 By MIohael addition Synthesis by RCM MIsoellaneous syntheses... [Pg.677]

In the utilization of petroleum oils in the field of chemical weed control, oils function as toxicants, as solvents, as filming agents, and as carriers. In view of the very effective synthetic compounds now used as toxicants (substituted phenols), the toxicity of the oils themselves is somewhat less important than it once was. Oils may serve as adjuvants in formulations involving 2,4-D, 2,4,5-T, dinitro compounds, trichloroacetates, and others. They have the unique property of aiding in the contact, spreading, and penetration of herbicides. In addition, synthesis of wetting agents, emulsifiers, and special herbicides may be dependent on petroleum products. [Pg.75]

When the additive synthesis is made by successive viewing, the same three-color images must be flashed onto the screen in such rapid succession that the individual red, green, and blue images are not apparent. Simple... [Pg.31]

Linear Synthesis. The most popular method of synthesis is so-called Additive Synthesis , where the output is a sum of oscillators. While it is commonly assumed that the oscillators produce sinusoids (Fourier synthesis), in fact, they can be any waveform. Furthermore, with static additive synthesis, a pre-mixed combination of harmonics was stored in the lookup table. Unfortunately, this doesn t permit inharmonic partials. Dynamic Fourier synthesis allows the amplitudes and frequencies of the partials to be varied relative to each other. Computationally, it is important to recognize the that updating oscillator coefficients for large numbers of oscillators can be expensive. [Pg.120]

This solution has the advantage of being very simple, but the drawback of being expensive in terms of calculations, even when tabulated sinusoids are used in Eq. (7.17). In fact, additive synthesis (of which Eq. (7.17) is an example) can be implemented at a much lower cost by use of the Fourier transform [Rodet and Depalle, 1992]. This last remark is a strong motivation for using the following alternative ... [Pg.161]

An early approach to music processing, referred to as additive synthesis [Moorer, 1977], used the sinusoidal model of a quasi-periodic music note... [Pg.189]

Depalle et al., 1993] Depalle, P., Garcia, G., and Rodet, X. (1993). Analysis of sound for additive synthesis Tracking of partials using hidden markov models. In Proc. 1993 Workshop on Applications of signal Processing to Audio and Acoustics, Mohonk Mountain House, New Paltz, NY. [Pg.256]

Finally, an additional synthesis of recent times (1971) comes from Lappert and his group (48). They treated an electron-rich olefinic system, such as 1, l, 3,3 -tetraphenyl-2,2 -biimidazolidinylidene, with a suitable complex compound. In this manner, they attained cleavage of the C=C double bond and attachment of the carbene fragment to the metal ... [Pg.8]

Hydroxyalkylation of Enolates with Carbonyl Compounds ( Aldol Addition ) Synthesis of /3-Hydroxyketones and /3-Hydroxyesters... [Pg.558]

N. Krause, A. Hoffmann-Roder, Recent Advances in Catalytic Enantioselective Michael Additions, Synthesis 2001, 171-196. [Pg.593]

Cholestyramine or colestipol (resins). These are compounds that bind bile acids the drop in hepatic reabsorption of bile acids releases a feedback inhibition, resulting in a greater amount of cholesterol being converted to bile acids to maintain a steady level in the circulation. Additionally, synthesis of LDL receptors increases to allow for the increased cholesterol uptake for bile acid synthesis the overall effect is a reduction in plasma cholesterol. [Pg.105]

An additional thermodynamic tool that acts in the direction opposite to mimicry has been named molecular symbiosis (Tolstoguzov 1999, 2002, 2003). High excluded volume of long rigid macromolecules underlies this phenomenon. Their presence in a mixed solution concentrates other cosolutes including globular proteins. For instance, molecular symbiosis, for example, due to addition of polysaccharides, can increase concentration of an enzyme without need for additional synthesis. [Pg.37]


See other pages where Additive synthesis is mentioned: [Pg.164]    [Pg.715]    [Pg.919]    [Pg.1223]    [Pg.1449]    [Pg.1595]    [Pg.184]    [Pg.107]    [Pg.182]    [Pg.407]    [Pg.134]    [Pg.123]    [Pg.264]    [Pg.31]    [Pg.32]    [Pg.195]    [Pg.189]    [Pg.289]    [Pg.458]    [Pg.171]    [Pg.223]    [Pg.715]    [Pg.919]    [Pg.1223]    [Pg.1449]    [Pg.1595]    [Pg.293]    [Pg.19]   
See also in sourсe #XX -- [ Pg.346 ]

See also in sourсe #XX -- [ Pg.140 , Pg.439 , Pg.442 , Pg.443 , Pg.444 , Pg.445 , Pg.446 ]

See also in sourсe #XX -- [ Pg.19 , Pg.41 ]




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1,1,3-Trihalides synthesis with addition

1-Thiadecalin synthesis via transannular addition

A synthesis with addition

A-aminonitriles, synthesis with addition of 1 C-atom

Acetylenic esters, synthesis of heterocycles through nucleophilic additions

Addition Diene syntheses, Michael

Addition of Carbenes to Alkenes Cyclopropane Synthesis

Addition reactions (continued synthesis

Addition reactions hydroxylamine synthesis

Addition synthesis

Addition synthesis

Addition to Primary Amines Synthesis of Isonitriles

Additives diamond synthesis

Additives, enolate synthesis, lithium diisopropylamide

Alanes synthesis with addition

Aldehydes (s. a. Aldehyde synthesis with addition

Aldehydes (s. a. Formyl synthesis with addition

Aldehydes synthesis with addition

Amides synthesis via haloborane addition to alkynes

Amines synthesis with addition

Anti-Markovnikov addition alcohol synthesis

Applications in Addition to Solid-state Syntheses

Atom transfer radical addition organic synthesis

Biodegradable addition polymers synthesis

Carboxylic acid amid synthesis with addition

Carboxylic synthesis with addition

Chemical synthesis additives

Combination, Synthesis, or Addition Reactions

Conjugate addition asymmetric synthesis

Conjugate addition reactions lithium enolate synthesis

Conjugated diene, 1,2-addition synthesis

Cyclopropanes synthesis via conjugate addition to oxazepines

Electrophilic addition reactions alkene synthesis

Electrophilic addition reactions alkyne synthesis

Electrophilic addition reactions synthesis

Enantioselective synthesis Michael addition

Enantioselective synthesis additives

Enone, conjugate carbonyl addition synthesis

Enone. conjugate addition reaction with synthesis

Enones, P-alkoxycyclic synthesis via Michael addition

Epoxide synthesis addition reactions

Equilenin, 11-oxomethyl ether synthesis via conjugate addition

Ethylene derivatives synthesis with addition

Glutamic acid synthesis via conjugate addition

Glutarates synthesis via Michael addition

Glutarates synthesis via ester enolate addition

Halides synthesis with addition

Halobutynols, addition reactions synthesis

Heterocycles synthesis of, through nucleophilic additions

Heterocyclic synthesis through nucleophilic additions

Heterocyclic synthesis through nucleophilic additions to acetylenic

Hydrocarbons, hydrocarbon synthesis with addition

Hydroxymethyl compounds synthesis with addition

Indole alkaloids synthesis via Michael addition

Intramolecular Michael addition synthesis

Iron, alkoxycyclohexadienylnucleophilic addition synthesis

Iron, cyclohexadienylnucleophilic addition synthesis

Isocyanate, addition reactions synthesis

Ketones synthesis with addition

Lactam synthesis oxidative addition

Lactone synthesis oxidative addition

Lactone synthesis oxidative addition processes

Macromonomer Synthesis by Addition Processes

Macromonomer synthesis, addition

Macromonomer synthesis, addition anionic polymerization

Macromonomer synthesis, addition processes

Michael addition in the synthesis

Michael addition stereoselective synthesis

Multicomponent Synthesis of Annelated Thiopyranones by Coupling-Addition-Nucleophilic Aromatic Substitution Sequence

Nitriles synthesis with addition

Nucleophilic addition Gabriel synthesis

Nucleophilic addition reactions phosphonium ylide synthesis

Nucleophilic additions to 1,3-dienes the synthesis of geranylacetone

Nucleophilic additions to acetylenic esters synthesis of heterocycles through

Nucleophilic additions to acetylenic esters, synthesis

Nucleophilic additions to acetylenic esters, synthesis of heterocycles

Organic Additives (Templates) in Synthesis of Zeolites and Molecular Sieves

Oxazole syntheses, additional

Oxidative addition organic synthesis

Oxidative addition reactions synthesis

Oxidative addition synthesis

Oxidative addition total synthesis

Oximes synthesis with addition

Reversible addition-fragmentation chain synthesis

Reversible addition-fragmentation chain transfer RAFT agent synthesis

Reversible addition-fragmentation chain transfer block copolymer synthesis

Reversible addition-fragmentation chain transfer star synthesis

Reversible addition-fragmentation polymer synthesis

Reversible addition-fragmentation synthesis

Reversible addition-fragmentation transfer synthesis

Ruthenium-catalyzed Addition of Organic Halides and Sulfonylchlorides in Polymer Synthesis ATRP

Ruthenium-catalyzed Addition of Sulfonyl Chlorides to Alkenes in Organic Synthesis

Sinusoidal Additive Synthesis

Spectral Modeling and Additive Synthesis

Stereoselective Syntheses of Chiral Piperidines via Addition Reactions to 4-Pyridones

Stereoselective addition synthesis

Stereoselective synthesis Stereospecific addition

Stereoselective synthesis conjugate addition

Stereoselective synthesis multiple bond additions

Stereoselective synthesis single bond additions

Study 6.8 Asymmetric synthesis diastereoselective photosensitized polar addition

Succinaldehyde synthesis via conjugate addition to imidazoline

Succinaldehyde, 3-alkylmethyl esters synthesis via copper catalyzed Grignard additions

Sulfonamides synthesis additions

Sulfonic acid esters synthesis with addition

Sulfur trioxide, addition compounds for synthesis

Synthesis 1,4-addition reactions with

Synthesis 1,4-addition reactions with cyanohydrin ethers

Synthesis 1,4-addition reactions with cyanohydrins

Synthesis Michael additions

Synthesis addition reactions

Synthesis conjugate addition

Synthesis diastereoselective additions

Synthesis of Glycosides by Addition Reactions

Synthesis of Heterocycles via X—H Bond Addition to Diynes

Synthesis of Siloles and Germoles via Double trans Addition to 1,3-Diynes

Synthesis of heterocycles through nucleophilic additions to acetylenic

Synthesis radical additions

Synthesis through nucleophilic additions

Synthesis with addition of 1 C-atom

Thiirane, 2,3-bis synthesis via thiocyanogen addition to alkene

Zinc, divinylenantioselective addition reactions synthesis

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