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Decker

C5HjMn(CO)3. Triple-decker derivatives are also known. See organomelallic compounds, metallocenes, ferrocene. [Pg.352]

M. L. White, in Clean Surfaces, Their Preparation and Characterization for Interfacial Studies, G. Goldfinger, ed., Marcel Decker, New York, 1970. [Pg.386]

Decker H and Sterner R 1990 Hierarchien in der Struktur und Funktion von sauerstoffbindenden Proteinen Naturwissensohaften 77 561 -8... [Pg.2847]

R. Paulson, A. Aquino, H. Decker, and T. Schapp, in I. J. Shapiro, ed.. Modem Utilisation of Infrared Technology VTII, SPIE Proceedings, Vol. 366, SPIE, Bellingham, Wash., 1983, pp. 88-95. [Pg.205]

J. Arhne, Rarpid Prototyping Rep. 1, 7 (1991) C. Decker, in P. K. T. Oldring, ed.. Chemistry andTechnology ofUV andEB Formulation for Coatings, Inks and Paints, Vol. 5, SITA Technologies, London, 1994, pp. 221—225 and references cited therein J. S. Amey, L. Sanders, and R. Hardesty,/ ImagingSd. Technol 38, 262 (1994). [Pg.396]

W. F. Erman, Studies in Organic Chemisty, Vol. 11, Chemistry of the Monoterpenes An Emyclopedic Handbook, Marcel Decker, New York, 1985. [Pg.434]

C. Decker, Effects of Grinding on Pigment Strength in Ceramic Glacis, presented at the 93rd aimual meeting, American Ceramic Society, Cincinnati, Ohio, May 1,1991 Ceram. Eng. Sci. Proc. to be pubhshed 1992. [Pg.431]

Trademarks, The Who What Where and How of Black oN Decker Trademarks, Black and Decker Manufacturiag Co., Towson, Md., 1987. [Pg.273]

FORSTER - DECKER Amine Synthesis Selective monoalkylation of primary amines via imines An altemativa method is the reaction ol 1 and 2 in the preserve of NaCNBH4 or tnaceloxyborohydride (Borch reduction)/... [Pg.127]

Decker, D.L., Bassett, W.A., Merrill, L., Hall, H.T., and Barnett, J.D., High-Pressure Calibration-Critical Review, J. Phys. Chem. Ref. Data 1 (3), 773-835... [Pg.366]

A composite material consists of flat, thin metal plates of uniform thickness glued one to another with a thin, epoxy-resin layer (also of uniform thickness) to form a multi-decker-sandwich structure. Young s modulus of the metal is Ej, that of the epoxy resin is E2 (where E2 < Ej) and the volume fraction of metal is Vj. Find the ratio of the maximum composite modulus to the minimum composite modulus in terms of Ej, E2 and V. Which value of gives the largest ratio ... [Pg.278]

Kokoszka, L. C., and Flood, J. W., "Environmental Management Handbook," Marcel Decker, New York, 1989. [Pg.443]

Decker, N., et al. Solution structure of the POU-specific DNA-binding domain of Oct-1. Nature 362 852-855, 1993. [Pg.173]

J. E. Brocklehurst, Fracture in Polycrystalline Graphite, In Chemistry and Physics of Carbon, Vol. 13, ed. Philip L. Walker, Jr. and Peter A Thrower, Marcel Decker, New York, 1977, pp. 145 279. [Pg.533]

The isomeric -cinnamylcocaine (methylcinnamoyl-d- -ecgonine) prepared by Einhorn and Deckers by the action of cinnamoyl chloride at 150-60° on d-i/r-ecgonine methyl ester, crystallises in prisms, m.p. 68°, [ Id + 2° (EtOH). The hydrochloride, B. HCl, forms needles, m.p. 186° the platinichloride, needles, m.p. 208°, and the aurichloride orange needles, m.p. 164°. [Pg.95]

In a similar attempt, Decker and Eichler reduced A -methylnor-papaverinium phenolbetaine (VIII) with tin and hydrochloric acid and obtained i/i-laudanine, m.p. 112°, pierate, m.p. 162-3°, which was subsequently investigated by Spath and Epstein, who showed that on methylation it furnished dMaudanosine and that the ethyl ether on energetic oxidation yielded veratric acid (3 4-dimethoxybenzoic acid) and the methyl ethyl ether of nor-m-hemipinic acid. This clearly indicated that the free hydroxyl group was in the woquinoline nucleus, and its position was determined by the fact that on mild oxidation 7-methoxy-6-ethoxy-l-keto-2-methyl-l 2 3 4-tetrahydrowoquinoline, m.p. 95-6°, was produced, and on this basis these authors assigned formula (IX R = H R = CH3) to -laudanine. [Pg.194]


See other pages where Decker is mentioned: [Pg.358]    [Pg.384]    [Pg.459]    [Pg.227]    [Pg.482]    [Pg.505]    [Pg.102]    [Pg.396]    [Pg.396]    [Pg.207]    [Pg.59]    [Pg.435]    [Pg.470]    [Pg.8]    [Pg.34]    [Pg.25]    [Pg.73]    [Pg.375]    [Pg.18]    [Pg.161]    [Pg.161]    [Pg.161]    [Pg.161]    [Pg.127]    [Pg.333]    [Pg.667]    [Pg.756]    [Pg.756]    [Pg.166]    [Pg.168]    [Pg.168]    [Pg.191]    [Pg.198]   
See also in sourсe #XX -- [ Pg.127 ]

See also in sourсe #XX -- [ Pg.35 , Pg.41 ]

See also in sourсe #XX -- [ Pg.78 ]

See also in sourсe #XX -- [ Pg.107 ]

See also in sourсe #XX -- [ Pg.107 ]




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Black and Decker

C2B3 Ring Double-decker Sandwiches

C2B3 Ring Triple-decker Sandwiches

C3B2 Ring Double-decker Sandwiches

C3B2 Ring Triple-decker Sandwiches and Dimers

C5B Ring Dinuclear Complexes (Triple-decker Sandwiches and Dimers)

C5B Ring Double-decker Sandwiches

Cerium double decker

Cobalt neutral and charged triple-decker

Cobalt-iron triple-decker complexes

Cyclopentadienyl complex triple-decker sandwich

Decker equation

Decker oxidation

Decker oxidation salts

Double-decker complexes

Double-decker lanthanide complexes

Double-decker ligands

Double-decker porphyrins

Double-decker sandwich compound

Double-decker shaped silsesquioxane

Double-decker silsesquioxane

FORSTER ’ DECKER Amine synthesis

Forster-Decker

Multi-decker ligands

Multi-decker sandwich

Multiple-decker sandwich

Nickel complex triple-decker sandwich

Phthalocyanine triple decker complexes

Phthalocyanine triple-decker structure

Preparation of Triple-Decker Cyclopentadienyl Complexes

Ruthenium-osmium triple decker complexes

Sandwich compounds multiple-decker

Sandwiches and Triple-deckers

Tetra-decker sandwich complexes

Triple decker sandwich compounds

Triple-decker

Triple-decker cobalt-metal complexes

Triple-decker cobalt-metal complexes synthesis

Triple-decker complexe

Triple-decker complexes

Triple-decker porphyrin complex

Triple-decker sandwich complexes

Triple-decker sandwich complexes bonding

Triple-decker sandwiches

Tris rare earth triple-decker

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