Author Topic: 2012 Reference Requests  (Read 1680 times)

RoidRage

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Re: Wanted References and Translations January 2012
« Reply #20 on: February 04, 2012, 07:31:40 PM »
Requested by fatfreddy

Protective effect of green tea polyphenol EGCG against neuronal damage and brain edema after unilateral cerebral ischemia in gerbils

Hyung Lee, Jae Hoon Bae, Seong-Ryong Lee
Journal of Neuroscience Research
Volume 77, Issue 6, pages 892–900, 15 September 2004
DOI: 10.1002/jnr.20193

java

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Re: Wanted References and Translations January 2012
« Reply #21 on: February 05, 2012, 08:43:27 AM »
Requested by Assyl Fartrate



MORPHINE DERIVATIVES WITH ANTIANALGESIC ACTION
A. F. Green, G. K. Ruffell, E. Walton
Journal of Pharmacy and Pharmacology
1954, Volume 6, Issue 1, pages 390–397
DOI: 10.1111/j.2042-7158.1954.tb10960.x
« Last Edit: February 05, 2012, 08:46:06 AM by java »
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java

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Re: Wanted References and Translations February 2012
« Reply #22 on: February 06, 2012, 03:31:38 AM »
Requested b Assyl Fartrate


Synthesis and Biological Evaluation of 14-Alkoxymorphinans. Part 19
Effect of 14-O-Benzylation on the Opioid Receptor Affinity and Antagonist Potency of Naltrexone

Falko Schüllner, Ruth Meditz,
Helvetica Chimica Acta
2003, Volume 86, Issue 7, pages 2335–2341
DOI: 10.1002/hlca.200390187




Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 22.1 Influence of the 14-Alkoxy Group and the Substitution in Position 5 in 14-Alkoxymorphinan-6-ones on in Vitro and in Vivo Activities
Roberta Lattanzi, Mariana Spetea,
J. Med. Chem.
2005, 48 (9), pp 3372–3378
DOI: 10.1021/jm040894o



« Last Edit: February 06, 2012, 03:37:26 AM by java »
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java

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Re: Wanted References and Translations February 2012
« Reply #23 on: February 06, 2012, 04:06:35 AM »
Requested by no1uno


Dehydration of 1,2-propanediol to propionaldehyde over zeolite catalysts
Dazhi Zhang, Sami A.I. Barri & David Chadwick
App.Cat.A:General
Vol.400(1) 2011 pp.148-155
DOI: http://dx.doi.org/10.1016/j.apcata.2011.04.028

Abstract

Dehydration of 1,2-propanediol has been investigated over a range of zeolite catalysts with different pore structures and acidity. The reaction forms part of a two-step process for the conversion of glycerol to propionaldehyde. The effects of reaction temperature, concentration, space velocity, and SiO2/Al2O3 ratio have been studied. The medium pore size, unidirectional channel zeolites ZSM-23 and Theta-1 showed high activity and selectivity to propionaldehyde (exceeding 90 wt% at 300–350 °C). Selectivity to the intermolecular dehydration product 2-ethyl-4-methyl-1,3-dioxolane was high at lower temperatures for all the zeolites, but decreased to a low value at higher temperatures and lower GHSV. The results are discussed in relation to the reaction mechanism and zeolite structures. Significant deactivation was observed for higher 1,2-propanediol partial pressures, which was partially mitigated by the addition of steam.





Catalytic dehydration of 1,2-propanediol into propanal
Keitaro Mori, Yasuhiro Yamada & Satoshi Sato
App.Cat.A:General
Vol.366(2) 2009 pp.304-308
DOI: http://dx.doi.org/10.1016/j.apcata.2009.07.018

Abstract

Vapor-phase catalytic dehydration of 1,2-propanediol was investigated over several catalysts, such as acidic oxides and supported heteropoly acids. These acids catalyze the dehydration of 1,2-propanediol to produce propanal. In particular, silica-supported silicotungstic acid showed the highest catalytic activity in the formation of propanal. At low conversions, however, propanal reacted with another 1,2-propanediol to produce a cyclic acetal (2-ethyl-4-methyl-1,3-dioxolane). Such acetal formation reduced the selectivity to propanal. Under optimum reaction conditions, 100% conversion was attained with propanal selectivity higher than 93 mol% at 200 °C.

Commemt by Requeste

May be useful - propionic acid is available, n-propanol not so much and n-propanal not really at all... Three carbon building blocks might be useful one day
« Last Edit: February 06, 2012, 04:11:31 AM by java »
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java

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Re: Wanted References and Translations February 2012
« Reply #24 on: February 06, 2012, 04:11:53 PM »
Requested by Assyl Fartrate


Efficient N-Demethylation of Opiate Alkaloids Using a Modified Nonclassical Polonovski Reaction
Kristy McCamley, Justin A. Ripper
J. Org. Chem.
2003, 68 (25), pp 9847–9850
DOI: 10.1021/jo035243z




Two-Step Iron(0)-Mediated N-Demethylation of N-Methyl Alkaloids
Gaik B. Kok, Cory C. Pye
J. Org. Chem.
2010, 75 (14), pp 4806–4811
DOI: 10.1021/jo1008492





New Methodology for the N-Demethylation of Opiate Alkaloids
Zemin Dong and Peter J. Scammells
J. Org. Chem.
2007, 72 (26), pp 9881–9885
DOI: 10.1021/jo071171q


« Last Edit: February 06, 2012, 04:17:54 PM by java »
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Re: Wanted References and Translations February 2012
« Reply #25 on: February 06, 2012, 10:18:14 PM »
Requested by Assyl Fartrate



The pharmacology of 14-hydroxyazidomorphine
J. KNOLL,SUSANNA FÜRST, S. MAKLEIT
Journal of Pharmacy and Pharmacology
1975, Volume 27, Issue 2, pages 99–105
DOI: 10.1111/j.2042-7158.1975.tb09416.x[/color]

Comment by Requestee

This paper was cited in this passage of another title...

Quote
Acylation of the alcohol at position 14 by cinnamoyl leads to a major
increase in potency. This product (44) shows 70-100 times the potency
of morphine even though the oxygen atom at 3 is present as the methyl
ether.
« Last Edit: February 06, 2012, 10:22:07 PM by java »
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Re: Wanted References and Translations February 2012
« Reply #26 on: February 07, 2012, 03:00:58 AM »
Requested by Assyl Fartrate


Some pharmacological studies with 14-cinnamoyloxycodeinone
W. R. Buckett
Journal of Pharmacy and Pharmacology
1965, Volume 17, Issue 11, pages 759–760
DOI: 10.1111/j.2042-7158.1965.tb07602.x


Note ....please first use the search engine to find the desired article, before you make a request.....this article already exists in our database......
« Last Edit: February 07, 2012, 06:31:32 AM by java »
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Re: Wanted References and Translations February 2012
« Reply #27 on: February 08, 2012, 10:12:05 PM »
Requested by Organikum



Heterogeneous permanganate oxidation of styrene and cinnamic acid derivatives: a simple and effective method for the preparation of benzaldehydes
S. Lai and D. G. Lee
Synthesis
2001, 11, 1645-1648.
DOI:10.1055/s-2001-16760
« Last Edit: February 08, 2012, 10:14:23 PM by java »
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RoidRage

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Re: Wanted References and Translations February 2012
« Reply #28 on: February 09, 2012, 05:51:55 PM »
Requested by Assyl Fartrate

14-Hydroxylation of Opiates: Catalytic Direct Autoxidation of Codeinone to 14-Hydroxycodeinone
Qibo Zhang, Joseph O. Rich, Ian C. Cotterill, David P. Pantaleone, and Peter C. Michels
J. Am. Chem. Soc., 2005, 127 (20), pp 7286–7287
DOI: 10.1021/ja051682z

RoidRage

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Re: Wanted References and Translations February 2012
« Reply #29 on: February 13, 2012, 06:47:27 PM »
Requested by no1uno

Influence of pH of an aqueous-organic solvent on the kinetics of N-acylation of a-amino acids with benzoic acid esters
L. V. Kuritsyn, A. I. Sadovnikov, L. N. Khripkova, N. V. Kalinina and Yu. S. Shcherbakova
Russ.J.Gen.Chem
Vol.76(1) 2006 pp.45-47
DOI: 10.1134/S1070363206010105


Studies of the rates of Thermal Decomposition of Glycine, Alanine and Serine

V.Ya. Yablokov, I.L. Smel'tsova, I.A. Zelyaev and S.V. Mitrofanova
Russ.J.Gen.Chem
Vol.79(8) 2009 pp.1704-1706
DOI: 10.1134/S1070363209080209



« Last Edit: February 17, 2012, 01:32:44 AM by RoidRage »

RoidRage

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Re: Wanted References and Translations February 2012
« Reply #30 on: February 13, 2012, 06:51:49 PM »
Requested by Assyl Fartrate

REDUCTION STUDIES IN THE MORPHINE SERIES. IX. HYDROXYCODEINONE
ROBERT E. LUTZ, LYNDON SMALL
J. Org. Chem., 1939, 04 (3), pp 220–233
DOI: 10.1021/jo01215a002


Hydroxylated Codeine Derivatives
LEWIS J. SARGENT, LOUIS H. SCHWARTZMAN, LYNDON F. SMALL
J. Org. Chem., 1958, 23 (9), pp 1247–1251
DOI: 10.1021/jo01103a003
« Last Edit: February 13, 2012, 07:18:12 PM by RoidRage »

RoidRage

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Re: Wanted References and Translations February 2012
« Reply #31 on: February 17, 2012, 01:30:43 AM »
Requested by no1uno

Thermal Decomposition of Some Amino Acids: Alanine and B-Alanine
Y.C. Lien and W.W. Nawar
Gen. & Intro. Food Sci. & Tech.
Vol.39(5) 1974 pp.914-916
DOI: 10.1111/j.1365-2621.1974.tb07275.x

« Last Edit: February 17, 2012, 01:34:05 AM by RoidRage »

RoidRage

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Re: Wanted References and Translations February 2012
« Reply #32 on: February 20, 2012, 07:37:00 PM »
Requested by fishinabottle


Readily Made Solvated Electrons
Ibanez, Jorge G.; Guerra-Millan, Francisco J.; Hugerat, Muhamad; Vazquez-Olavarrieta, Jorge L.; Basheer, Ahmad; Abu-Much, Riam
Journal of Chemical Education, vol. 88, issue 5, pp. 670-672
DOI: 10.1021/ed100179d

Solvated Electrons in Organic Chemistry Laboratory
redrag-Peter Ilich*, Kathleen R. McCormick, Adam D. Atkins, Geoffrey J. Mell, Timothy J. Flaherty, Martin J. Bruck, Heather A. Goodrich and Aaron L. Hefel
Division of Molecular and Life Sciences, Loras College, Dubuque, Iowa 52001
Nenad Juranic? Department of Biochemistry and Molecular Biology, Mayo Foundation, Rochester, Minnesota 55905 Suzanne Seleem Department of Natural Sciences, Mathematics and Computers, Central State University, Wilberforce, Ohio 45384
J. Chem. Educ., 2010, 87 (4), pp 419–422
DOI: 10.1021/ed800093n

RoidRage

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Re: Wanted References and Translations February 2012
« Reply #33 on: February 22, 2012, 01:33:17 AM »
Requested by dream0n

The Degradation Of Carboxylic Acid Salts By Means Of Halogen - The Hunsdiecker Reaction
Chem. Rev., 1956, 56 (2), pp 219–269
DOI: 10.1021/cr50008a002
Publication Date: April 1956

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Re: Wanted References and Translations February 2012
« Reply #34 on: February 22, 2012, 01:55:42 AM »
Requested by fishinabottle l

Review on the electrochemistry of solvated electrons. Its use in hydrogenation of monobenzenoids
P. J. M. van Andel-Scheffer, E. Barendrecht
Recueil des Travaux Chimiques des Pays-Bas
Volume 114, Issue 6, pages 259–265, 1995
DOI: 10.1002/recl.19951140602[/color]


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RoidRage

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Re: Wanted References and Translations February 2012
« Reply #35 on: February 23, 2012, 06:53:08 PM »
Requested by EverlastingReign


Styrene: Its polymers, copolymers and derivatives

J. Chem. Educ., 1953, 30 (4), p 216
DOI: 10.1021/ed030p216.2
Publication Date: April 1953
 

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Re: Wanted References and Translations February 2012
« Reply #36 on: February 26, 2012, 12:13:57 PM »
Requested by no1uno



The Acidities of Ketones and the Mechanism of Prototropic Change
H. B. Watson, W. S. Nathan, and L. L. Laurie
J.Chem.Phys.
1935, Vol.3, pp.170-174
DOI: http://dx.doi.org/10.1063/1.1749627


Abstract
The observation of acidity in the brominated acetones is attributed to coordination of carbonyl carbon and hydroxyl ion, the process being preceded by electromeric change to the semipolar form. Acid? and base?catalyzed prototropy is regarded as involving a similar electromeric change, brought about by interaction with the catalyst, and followed by transformation of the semipolar form either to ketone or to enolic ion. The measured velocity will thus be dependent upon (a) the rate of reaction of ketone and catalyst, and (b) the proportion of the semipolar form which changes to enol. The application of this view, in conjunction with the conception of quantum?mechanical resonance as developed by Pauling, renders possible the satisfactory interpretation of a number of observations relating to the prototropic changes of carbonyl compounds.


Comment by Requestee

I'm interested in this because the "google" results - Page 1, No.9 from the search terms "calcium phenylacetate acetate phenylacetone" reads:

  " phenylacetone undergoes prototropic change much more rapidly than does ... 59, 623 (1891», by very carefully regulated heating of calcium phenylacetate ..."
« Last Edit: February 26, 2012, 12:21:40 PM by java »
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java

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Re: Wanted References and Translations February 2012
« Reply #37 on: February 26, 2012, 09:09:28 PM »
Requested by RoidRage


Effects of ethanol on formation of inclusion complexes of hydroxypropylcyclodextrins with testosterone or with methyl orange
Josef Pitha,Teruhiko Hoshino
International Journal of Pharmaceutics
1992, Volume 80, Issues 1–3, 25 February, Pages 243–251
DOI :10.1016/0378-5173(92)90281-6
« Last Edit: February 26, 2012, 09:11:51 PM by java »
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RoidRage

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Re: Wanted References and Translations February 2012
« Reply #38 on: March 07, 2012, 06:38:49 AM »
Requested by no1uno


Production of sodium borohydride by using dynamic behaviors of protide at the extreme surface of magnesium particles
S. Suda, N. Morigasaki, Y. Iwase & Z.P. Li
J. Alloys & Cmpds
Vol.404-406 (2005) pp.643-647
http://dx.doi.org/10.1016/j.jallcom.2005.02.101

Abstract

An advanced process for the production of sodium borohydride (NaBH4) as a hydrogen storage material was developed, which applied the dynamic hydriding and dehydriding behaviors of protide (H-) in Mg–H system under transitional temperature conditions.

An abundant natural resource named borax (Na2B4O7·10H2O) and the anhydrous sodium metaborate (NaBO2) recovered from the “spent fuel” as NaBO2·4H2O were used as the starting material in the present process. Powder-state Mg played an important role in the transitional hydriding and dehydriding process where the gaseous hydrogen was converted to protide at the extreme surface of Mg to form NaBH4 in exchange with the simultaneous transition of oxygen in NaBO2 to form MgO.

In the present process, the protide as the most reactive state among the four states of hydrogen is applied for the synthesis of NaBH4, which can exist in metal–hydrogen complexes, such as NaAlH4 and NaBH4.

The NaBH4 yield was reached higher than 90% by a single batch process but was found to be largely dependent on the rate of temperature change and the particle size, i.e., the specific surface area of Mg particles.




Sodium borohydride formation when Mg reacts with hydrous sodium borates under hydrogen

Bin Hong Liu, Zhou Peng Li & Jing Ke Zhu
J. Alloys & Cmpds
Vol.476(1-2) 2009 pp.L16-L20
http://dx.doi.org/10.1016/j.jallcom.2008.09.057

Abstract

In this work, we explored the possibility of NaBH4 synthesis when Mg reacted with hydrous sodium borates under hydrogen. It was found that Mg could react with the water in molten hydrous borates to form MgO and release hydrogen, which can be used for NaBH4 synthesis. Then remained Mg would react with formed anhydrous borate to form NaBH4. NaBO2 conversion rate was decreased with increase of the crystalline water content in the hydrous sodium borates. Based on experimental results, a mechanism of NaBH4 formation when Mg reacted with hydrous sodium borates was suggested.



NaBH4 formation mechanism by reaction of sodium borate with Mg and H2

Z.P. Li, B.H. Liu, J.K. Zhu, N. Morigasaki & S. Suda
J. Alloys & Cmpds
Vol.437(1-2) 2007 pp.311-316
http://dx.doi.org/10.1016/j.jallcom.2006.07.119

Abstract

It has been reported that sodium (potassium) borohydride can be formed by reaction of sodium (potassium) borate with Mg and hydrogen or magnesium hydride. However, few investigations on reaction mechanism have been reported. Here, we studied the NaBH4 formation mechanism of Mg + NaBO2 + 2H2 = NaBH4 + MgO through morphology observations, structure and micro composition analyses. It was found that when heating the reactor to 400 °C, NaBO2 particles were agglomerated with Mg particles and a NaBO2 network was formed due to the sintering effect. With further heating the reactor, a porous product layer (composed of NaBH4 and MgO) was formed on Mg particles. It was found that no matter whether Mg was hydrogenated or not, Mg could react with sodium borate and hydrogen to form sodium borohydride. Elevating the reaction temperature was of benefit to NaBH4 formation. Higher NaBH4 yield can be obtained by using partially hydrogenated then dehydrogenated Mg.




RoidRage

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Re: Wanted References and Translations February 2012
« Reply #39 on: March 07, 2012, 10:31:45 PM »
Requested by Assyl Fartrate

Synthesis of cyclic ?-dimaines
I. N. Nazarov and N. V. Kuznetsov
Russian Chemical Bulletin
Volume 7, Number 4, 501-503, DOI: 10.1007/BF00910947