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New experiments with movable calorimetric bomb.

Acta chemica Scandinavica

SMITH L, BJELLERUP L.
PMID: 18907699
Acta Chem Scand. 1947;1(6):566-70.

No abstract available.

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SMITH L, BJELLERUP L. Neue Versuche mit beweglicher calorimetrischer Bombe. New experiments with movable calorimetric bomb. Acta Chem Scand. 1947;1(6):566-70
SMITH, L., & BJELLERUP, L. (1947). Neue Versuche mit beweglicher calorimetrischer Bombe. New experiments with movable calorimetric bomb. Acta chemica Scandinavica, 1(6), 566-70.
SMITH, L, and BJELLERUP, L. "Neue Versuche mit beweglicher calorimetrischer Bombe." New experiments with movable calorimetric bomb. Acta chemica Scandinavica vol. 1,6 (1947): 566-70.
SMITH L, BJELLERUP L. Neue Versuche mit beweglicher calorimetrischer Bombe. New experiments with movable calorimetric bomb. Acta Chem Scand. 1947;1(6):566-70. German. PMID: 18907699.
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Morphine hydro-chloride anhydrate.

Acta crystallographica. Section E, Structure reports online

Gelbrich T, Braun DE, Griesser UJ.
PMID: 23476193
Acta Crystallogr Sect E Struct Rep Online. 2012 Dec 01;68:o3358-9. doi: 10.1107/S1600536812046405. Epub 2012 Nov 17.

In the title mol-ecular salt [systematic name: (5α,6α)-7,8-didehydro-4,5-ep-oxy-17-methyl-morphinan-3,6-diol hydro-chloride], C17H20NO3(+)·Cl(-), the conformation of the morphinium ion is in agreement with the characteristics of the previously reported morphine forms [for example, Gylbert (1973 ▶). Acta Cryst. B29, 1630-1635]. In the...

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Gelbrich T, Braun DE, Griesser UJ. Morphine hydro-chloride anhydrate. Acta Crystallogr Sect E Struct Rep Online. 2012;68:o3358-9doi: 10.1107/S1600536812046405.
Gelbrich, T., Braun, D. E., & Griesser, U. J. (2012). Morphine hydro-chloride anhydrate. Acta crystallographica. Section E, Structure reports online, 68o3358-9. https://doi.org/10.1107/S1600536812046405
Gelbrich, Thomas, et al. "Morphine hydro-chloride anhydrate." Acta crystallographica. Section E, Structure reports online vol. 68 (2012): o3358-9. doi: https://doi.org/10.1107/S1600536812046405
Gelbrich T, Braun DE, Griesser UJ. Morphine hydro-chloride anhydrate. Acta Crystallogr Sect E Struct Rep Online. 2012 Dec 01;68:o3358-9. doi: 10.1107/S1600536812046405. Epub 2012 Nov 17. PMID: 23476193; PMCID: PMC3588957.
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Crystal structure of Hg2SO4 - a redetermination.

Acta crystallographica. Section E, Structure reports online

Weil M.
PMID: 25309168
Acta Crystallogr Sect E Struct Rep Online. 2014 Aug 01;70:i44. doi: 10.1107/S1600536814011155. eCollection 2014 Sep 01.

The crystal structure of mercury(I) sulfate (or mercurous sulfate), Hg2SO4, was re-determined based on modern CCD data. In comparison with the previous determination from Weissenberg film data [Dorm (1969 ▶). Acta Chem. Scand. 23, 1607-1615], all atoms were refined...

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Weil M. Crystal structure of Hg2SO4 - a redetermination. Acta Crystallogr Sect E Struct Rep Online. 2014;70:i44doi: 10.1107/S1600536814011155.
Weil, M. (2014). Crystal structure of Hg2SO4 - a redetermination. Acta crystallographica. Section E, Structure reports online, 70i44. https://doi.org/10.1107/S1600536814011155
Weil, Matthias. "Crystal structure of Hg2SO4 - a redetermination." Acta crystallographica. Section E, Structure reports online vol. 70 (2014): i44. doi: https://doi.org/10.1107/S1600536814011155
Weil M. Crystal structure of Hg2SO4 - a redetermination. Acta Crystallogr Sect E Struct Rep Online. 2014 Aug 01;70:i44. doi: 10.1107/S1600536814011155. eCollection 2014 Sep 01. PMID: 25309168; PMCID: PMC4186147.
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Sequence of Reactant Combination Alters the Course of the Staudinger Reaction of Azides with Acyl Derivatives. Bimanes. 30.

The Journal of organic chemistry

Shalev DE, Chiacchiera SM, Radkowsky AE, Kosower EM.
PMID: 11667038
J Org Chem. 1996 Mar 08;61(5):1689-1701. doi: 10.1021/jo950273q.

The Staudinger reaction of azides has now been followed by NMR and other spectroscopic techniques. syn-(Azidomethyl,methyl)(methyl,methyl)bimane (1) and Ph(3)P form a triazaphosphadiene intermediate 2 and then the bimane P-triphenyliminophosphorane 3. The iminophosphorane reacts with an acyl chloride to yield...

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Shalev DE, Chiacchiera SM, Radkowsky AE, et al. Sequence of Reactant Combination Alters the Course of the Staudinger Reaction of Azides with Acyl Derivatives. Bimanes. 30. J Org Chem. 1996;61(5):1689-1701doi: 10.1021/jo950273q.
Shalev, D. E., Chiacchiera, S. M., Radkowsky, A. E., & Kosower, E. M. (1996). Sequence of Reactant Combination Alters the Course of the Staudinger Reaction of Azides with Acyl Derivatives. Bimanes. 30. The Journal of organic chemistry, 61(5), 1689-1701. https://doi.org/10.1021/jo950273q
Shalev, Deborah E., et al. "Sequence of Reactant Combination Alters the Course of the Staudinger Reaction of Azides with Acyl Derivatives. Bimanes. 30." The Journal of organic chemistry vol. 61,5 (1996): 1689-1701. doi: https://doi.org/10.1021/jo950273q
Shalev DE, Chiacchiera SM, Radkowsky AE, Kosower EM. Sequence of Reactant Combination Alters the Course of the Staudinger Reaction of Azides with Acyl Derivatives. Bimanes. 30. J Org Chem. 1996 Mar 08;61(5):1689-1701. doi: 10.1021/jo950273q. PMID: 11667038.
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RElationships between rapid equilibrium conditions and linearization of the reciprocal rate equation for the sequential random two-substrate enzyme mechanism.

Acta chemica Scandinavica

Pettersson G.
PMID: 5381399
Acta Chem Scand. 1969;23(9):3243-7. doi: 10.3891/acta.chem.scand.23-3243.

No abstract available.

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Pettersson G. RElationships between rapid equilibrium conditions and linearization of the reciprocal rate equation for the sequential random two-substrate enzyme mechanism. Acta Chem Scand. 1969;23(9):3243-7doi: 10.3891/acta.chem.scand.23-3243.
Pettersson, G. (1969). RElationships between rapid equilibrium conditions and linearization of the reciprocal rate equation for the sequential random two-substrate enzyme mechanism. Acta chemica Scandinavica, 23(9), 3243-7. https://doi.org/10.3891/acta.chem.scand.23-3243
Pettersson, G. "RElationships between rapid equilibrium conditions and linearization of the reciprocal rate equation for the sequential random two-substrate enzyme mechanism." Acta chemica Scandinavica vol. 23,9 (1969): 3243-7. doi: https://doi.org/10.3891/acta.chem.scand.23-3243
Pettersson G. RElationships between rapid equilibrium conditions and linearization of the reciprocal rate equation for the sequential random two-substrate enzyme mechanism. Acta Chem Scand. 1969;23(9):3243-7. doi: 10.3891/acta.chem.scand.23-3243. PMID: 5381399.
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A new method for the synthesis of arylstibonic compounds.

Acta chemica Scandinavica

VOIGT AF.
PMID: 20269027
Acta Chem Scand. 1947;1(1):118. doi: 10.3891/acta.chem.scand.01-0118.

No abstract available.

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VOIGT AF. A new method for the synthesis of arylstibonic compounds. Acta Chem Scand. 1947;1(1):118doi: 10.3891/acta.chem.scand.01-0118.
VOIGT, A. F. (1947). A new method for the synthesis of arylstibonic compounds. Acta chemica Scandinavica, 1(1), 118. https://doi.org/10.3891/acta.chem.scand.01-0118
VOIGT, A F. "A new method for the synthesis of arylstibonic compounds." Acta chemica Scandinavica vol. 1,1 (1947): 118. doi: https://doi.org/10.3891/acta.chem.scand.01-0118
VOIGT AF. A new method for the synthesis of arylstibonic compounds. Acta Chem Scand. 1947;1(1):118. doi: 10.3891/acta.chem.scand.01-0118. PMID: 20269027.
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Use of electron multiplier cells in Raman spectrography.

Acta chemica Scandinavica

KINELL O, TRAYNARD P.
PMID: 18098528
Acta Chem Scand. 1948;2(3):193-203.

No abstract available.

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KINELL O, TRAYNARD P. Utilisation des cellules multiplicateurs d'electrons en spectrographie raman. Use of electron multiplier cells in Raman spectrography. Acta Chem Scand. 1948;2(3):193-203
KINELL, O., & TRAYNARD, P. (1948). Utilisation des cellules multiplicateurs d'electrons en spectrographie raman. Use of electron multiplier cells in Raman spectrography. Acta chemica Scandinavica, 2(3), 193-203.
KINELL, O, and TRAYNARD, P. "Utilisation des cellules multiplicateurs d'electrons en spectrographie raman." Use of electron multiplier cells in Raman spectrography. Acta chemica Scandinavica vol. 2,3 (1948): 193-203.
KINELL O, TRAYNARD P. Utilisation des cellules multiplicateurs d'electrons en spectrographie raman. Use of electron multiplier cells in Raman spectrography. Acta Chem Scand. 1948;2(3):193-203. French. PMID: 18098528.
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Corticotropin, a pigment from the mycelium of a mycorrhizal fungus.

Acta chemica Scandinavica

ERDTMAN H.
PMID: 18098530
Acta Chem Scand. 1948;2(3):209-19.

No abstract available.

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ERDTMAN H. Corticrocin, a pigment from the mycelium of a mycorrhiza fungas. Corticotropin, a pigment from the mycelium of a mycorrhizal fungus. Acta Chem Scand. 1948;2(3):209-19
ERDTMAN, H. (1948). Corticrocin, a pigment from the mycelium of a mycorrhiza fungas. Corticotropin, a pigment from the mycelium of a mycorrhizal fungus. Acta chemica Scandinavica, 2(3), 209-19.
ERDTMAN, H. "Corticrocin, a pigment from the mycelium of a mycorrhiza fungas." Corticotropin, a pigment from the mycelium of a mycorrhizal fungus. Acta chemica Scandinavica vol. 2,3 (1948): 209-19.
ERDTMAN H. Corticrocin, a pigment from the mycelium of a mycorrhiza fungas. Corticotropin, a pigment from the mycelium of a mycorrhizal fungus. Acta Chem Scand. 1948;2(3):209-19. PMID: 18098530.
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The synthesis of 1,2-Diiodoethene.

Acta chemica Scandinavica

PAPPAS AC.
PMID: 18100065
Acta Chem Scand. 1948;2(3):292-4. doi: 10.3891/acta.chem.scand.02-0292.

No abstract available.

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PAPPAS AC. The synthesis of 1,2-Diiodoethene. Acta Chem Scand. 1948;2(3):292-4doi: 10.3891/acta.chem.scand.02-0292.
PAPPAS, A. C. (1948). The synthesis of 1,2-Diiodoethene. Acta chemica Scandinavica, 2(3), 292-4. https://doi.org/10.3891/acta.chem.scand.02-0292
PAPPAS, A C. "The synthesis of 1,2-Diiodoethene." Acta chemica Scandinavica vol. 2,3 (1948): 292-4. doi: https://doi.org/10.3891/acta.chem.scand.02-0292
PAPPAS AC. The synthesis of 1,2-Diiodoethene. Acta Chem Scand. 1948;2(3):292-4. doi: 10.3891/acta.chem.scand.02-0292. PMID: 18100065.
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A modification of the microhydrogenation apparatus of Breitschneider and Burger.

Acta chemica Scandinavica

CLAUSON-KAAS N, LIMBORG F.
PMID: 18876906
Acta Chem Scand. 1947;1(10):884-8. doi: 10.3891/acta.chem.scand.01-0884.

No abstract available.

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CLAUSON-KAAS N, LIMBORG F. A modification of the microhydrogenation apparatus of Breitschneider and Burger. Acta Chem Scand. 1947;1(10):884-8doi: 10.3891/acta.chem.scand.01-0884.
CLAUSON-KAAS, N., & LIMBORG, F. (1947). A modification of the microhydrogenation apparatus of Breitschneider and Burger. Acta chemica Scandinavica, 1(10), 884-8. https://doi.org/10.3891/acta.chem.scand.01-0884
CLAUSON-KAAS, N, and LIMBORG, F. "A modification of the microhydrogenation apparatus of Breitschneider and Burger." Acta chemica Scandinavica vol. 1,10 (1947): 884-8. doi: https://doi.org/10.3891/acta.chem.scand.01-0884
CLAUSON-KAAS N, LIMBORG F. A modification of the microhydrogenation apparatus of Breitschneider and Burger. Acta Chem Scand. 1947;1(10):884-8. doi: 10.3891/acta.chem.scand.01-0884. PMID: 18876906.
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Simulation of an oscillatory reaction of alcohol dehydrogenase in an oil/water system.

Biophysical chemistry

Hideshima T.
PMID: 17014766
Biophys Chem. 1991 Feb;39(2):171-5. doi: 10.1016/0301-4622(91)85019-m.

With numerical analysis of the enzyme-catalyzed reaction in the so called 'ordered bi-bi' mechanism and the model presented by Theorell and Chance (Acta Chem. Scand. 5 (1951) 1127) for alcohol dehydrogenase, oscillations of the concentrations of coenzyme and intermediate...

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Hideshima T. Simulation of an oscillatory reaction of alcohol dehydrogenase in an oil/water system. Biophys Chem. 1991;39(2):171-5doi: 10.1016/0301-4622(91)85019-m.
Hideshima, T. (1991). Simulation of an oscillatory reaction of alcohol dehydrogenase in an oil/water system. Biophysical chemistry, 39(2), 171-5. https://doi.org/10.1016/0301-4622(91)85019-m
Hideshima, T. "Simulation of an oscillatory reaction of alcohol dehydrogenase in an oil/water system." Biophysical chemistry vol. 39,2 (1991): 171-5. doi: https://doi.org/10.1016/0301-4622(91)85019-m
Hideshima T. Simulation of an oscillatory reaction of alcohol dehydrogenase in an oil/water system. Biophys Chem. 1991 Feb;39(2):171-5. doi: 10.1016/0301-4622(91)85019-m. PMID: 17014766.
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Symmetry, pseudosymmetry and packing disorder in the alcohol solvates of L-leucyl-L-valine.

Acta crystallographica. Section B, Structural science

Görbitz CH, Torgersen E.
PMID: 10927344
Acta Crystallogr B. 1999 Feb 01;55:104-113. doi: 10.1107/s0108768198010192.

The dipeptide L-Leu-L-Val can crystallize as a hydrate in the hexagonal space group P6(5) [Görbitz & Gundersen (1996). Acta Chem. Scand. 50, 537-543], but forms 1:1 solvates when methanol, ethanol and 2-propanol are used as precipitating agents. The structures...

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Görbitz CH, Torgersen E. Symmetry, pseudosymmetry and packing disorder in the alcohol solvates of L-leucyl-L-valine. Acta Crystallogr B. 1999;55:104-113doi: 10.1107/s0108768198010192.
Görbitz, C. H., & Torgersen, E. (1999). Symmetry, pseudosymmetry and packing disorder in the alcohol solvates of L-leucyl-L-valine. Acta crystallographica. Section B, Structural science, 55104-113. https://doi.org/10.1107/s0108768198010192
Görbitz, and Torgersen. "Symmetry, pseudosymmetry and packing disorder in the alcohol solvates of L-leucyl-L-valine." Acta crystallographica. Section B, Structural science vol. 55 (1999): 104-113. doi: https://doi.org/10.1107/s0108768198010192
Görbitz CH, Torgersen E. Symmetry, pseudosymmetry and packing disorder in the alcohol solvates of L-leucyl-L-valine. Acta Crystallogr B. 1999 Feb 01;55:104-113. doi: 10.1107/s0108768198010192. PMID: 10927344.
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Showing 1 to 12 of 21 entries