Steps to make the people who fetch articles for you happy:
1) UTFSE for your article here and at other boards. You'd be surprised at the myriad articles that we have already fetched. If you find it somewhere else, and it's important for the community, start a thread about it or post it in the "Articles of Interest" thread.
2) Make sure that the article is already in digital format. If it isn't, include that fact with your request.
3) Color your requests blue, and provide the following required information so that we can use our limited time wisely retrieving your article instead of searching for the necessary information. Your article request probably won't be filled if you don't include a DOI. You can simply fill in the form below.Code: [Select][color=blue]Authors
[b]Article Title[/b]
[i]Journal Title[/i] [b]Year[/b], [u]Volume[/u](Issue):Page range
DOI:____
PMID:____
[u]Abstract[/u]
If you can find the abstract, paste it here.[/color]
An Example using a previously fetched article (not the greatest because Synlett uses the year as its volume number, but you get the point):
Li-Xiong Shao, Min Shi
N-Bromosuccinimide and Lithium Bromide: An Efficient Combination for the Dibromination of Carbon-Carbon Unsaturated Bonds
Synlett 2006, 2006(:1269-1271
DOI: 10.1055/s-2006-941558
PMID: None
Abstract
Compounds possessing unsaturated bonds such as alkenes, alkynes, allenes, and methylenecyclopropanes (MCPs) can be dibrominated within minutes by NBS and lithium bromide in THF at room temperature in good to excellent yields under mild conditions.
java
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- Posts: 783
java
- Global Moderator
- Foundress Queen
- Posts: 783
Requested by PetulantPapist
Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions
Kandasamy Jeyakumar, Dillip Kumar Chand
Tetrahedron Letters
Volume 45, Issue 24, 7 June 2004, Pages 4785–4787
Copper perchlorate: Efficient acetylation catalyst under solvent free conditions
Prodeep Phukan
Journal of Molecular Catalysis A: Chemical
Volume 255, Issues 1–2, 1 August 2006, Pages 275–282
http://dx.doi.org/10.1016/j.molcata.2006.04.026
Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions
Kandasamy Jeyakumar, Dillip Kumar Chand
Tetrahedron Letters
Volume 45, Issue 24, 7 June 2004, Pages 4785–4787
Copper perchlorate: Efficient acetylation catalyst under solvent free conditions
Prodeep Phukan
Journal of Molecular Catalysis A: Chemical
Volume 255, Issues 1–2, 1 August 2006, Pages 275–282
http://dx.doi.org/10.1016/j.molcata.2006.04.026
Baba_McKensey
- Subordinate Wasp
- Posts: 109
Need copies of these ozone related references.
J. Soc. Chem. Ind. London, 41, 70 R (1922);
The following two reactions are carried out in GAA:
Ann.Chim.(Paris), <7> 13, 123 (1898);
Chem. Ber., 48, 232 (1915)
J. Soc. Chem. Ind. London, 41, 70 R (1922);
The following two reactions are carried out in GAA:
Ann.Chim.(Paris), <7> 13, 123 (1898);
Chem. Ber., 48, 232 (1915)
RoidRage
- Dominant Queen
- Posts: 386
Requested by Baba_McKensey
Using Ozone in Organic Chemistry Lab - The Ozonolysis Of Eugenol
Bruce M. Branan , Joshua T. Butcher and Lawrence R. Olsen
J. Chem. Educ., 2007, 84 (12), p 1979
Publication Date (Web): December 1, 2007 (Article)
DOI: 10.1021/ed084p1979
Using Ozone in Organic Chemistry Lab - The Ozonolysis Of Eugenol
Bruce M. Branan , Joshua T. Butcher and Lawrence R. Olsen
J. Chem. Educ., 2007, 84 (12), p 1979
Publication Date (Web): December 1, 2007 (Article)
DOI: 10.1021/ed084p1979
POSEIDON
- Subordinate Wasp
- Posts: 116
Requested by Baba_McKensey
Helv. Chim. Acta, 8, 407 (1925);
Helv. Chim. Acta, 7, 71 (1924)
Helv. Chim. Acta, 8, 407 (1925);
Helv. Chim. Acta, 7, 71 (1924)
EU1920xy
- Larvae
- Posts: 12
Maybe someone has this interesting book, all liks i found are dead
John E. Lesch
The First Miracle Drugs: How the Sulfa Drugs Transformed Medicine
ISBN 019518775X
I know its not a article, but i think its good for historical purposes
John E. Lesch
The First Miracle Drugs: How the Sulfa Drugs Transformed Medicine
ISBN 019518775X
I know its not a article, but i think its good for historical purposes
RoidRage
- Dominant Queen
- Posts: 386
Requested by fresh1
One-Pot Conversion of Thebaine to Hydrocodone and Synthesis of Neopinone Ketal
Robert J. Carroll†, Hannes Leisch†, Lena Rochon†, Tomas Hudlicky*† and D. Phillip Cox‡
Department of Chemistry and Centre for Biotechnology, Brock University, 500 Glenridge Avenue, St. Catharines, ON, Canada, L2S 3A1, and Noramco Inc., 503 Carr Road, Suite 200, Wilmington, Delaware 19809
DOI: 10.1021/jo802454v
One-Pot Conversion of Thebaine to Hydrocodone and Synthesis of Neopinone Ketal
Robert J. Carroll†, Hannes Leisch†, Lena Rochon†, Tomas Hudlicky*† and D. Phillip Cox‡
Department of Chemistry and Centre for Biotechnology, Brock University, 500 Glenridge Avenue, St. Catharines, ON, Canada, L2S 3A1, and Noramco Inc., 503 Carr Road, Suite 200, Wilmington, Delaware 19809
DOI: 10.1021/jo802454v
java
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Requested by Sydenhams chorea
Über die quantitative Methoxylbestimmung
Wilhelm Kropatschek
MONATSHEFTE FÜR CHEMIE
1904, 25(6):583-592
DOI:10.1007/BF01525978
Über die quantitative Methoxylbestimmung
Wilhelm Kropatschek
MONATSHEFTE FÜR CHEMIE
1904, 25(6):583-592
DOI:10.1007/BF01525978
Wizard X
- Lord of the Realms
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The attached PDF has many "Solvent-Free Condition MW" reactions, including...
REDUCTION OF CARBONYL COMPOUNDS TO THE CORRESPONDING ALCOHOLS WITH ISOPROPANOL ON DEHYDRATED ALUMINA UNDER MICROWAVE IRRADIATION.
REDUCTION OF CARBONYL COMPOUNDS TO THE CORRESPONDING ALCOHOLS WITH ISOPROPANOL ON DEHYDRATED ALUMINA UNDER MICROWAVE IRRADIATION.
RoidRage
- Dominant Queen
- Posts: 386
Requested by Goldmember
REDUCTION OF CARBONYL COMPOUNDS TO THE CORRESPONDING ALCOHOLS WITH ISOPROPANOL ON DEHYDRATED ALUMINA UNDER MICROWAVE IRRADIATION
Synthetic Communications
Volume 32, Issue 14, 2002
DOI: 10.1081/SCC-120005436
F. Kazemia & A. R. Kiasata
Cannizzaro Reaction of the Cinnamon Aldehyde under Solvent-Free Condition
Petrochemical Industry Application 2007-01
DOI? CNKI:ISSN:1673-5285.0.2007-01-007
TIAN Danian,DING Runmei,LIU Wanyi
REDUCTION OF CARBONYL COMPOUNDS TO THE CORRESPONDING ALCOHOLS WITH ISOPROPANOL ON DEHYDRATED ALUMINA UNDER MICROWAVE IRRADIATION
Synthetic Communications
Volume 32, Issue 14, 2002
DOI: 10.1081/SCC-120005436
F. Kazemia & A. R. Kiasata
Cannizzaro Reaction of the Cinnamon Aldehyde under Solvent-Free Condition
Petrochemical Industry Application 2007-01
DOI? CNKI:ISSN:1673-5285.0.2007-01-007
TIAN Danian,DING Runmei,LIU Wanyi
RoidRage
- Dominant Queen
- Posts: 386
Requested by POSEIDON
Synthesis of aliphatic thiomorpholides by willgerodt-kindler reaction under solvent-free conditions
Kioumars Aghapoora, Hossein Reza Darabia, Kourosh Tabar-Heydara & Leila Nakhshaba
Sulfur Letters
Volume 25, Issue 6, 2002
pages 259-261
DOI:10.1080/02786110215846
Synthesis of aliphatic thiomorpholides by willgerodt-kindler reaction under solvent-free conditions
Kioumars Aghapoora, Hossein Reza Darabia, Kourosh Tabar-Heydara & Leila Nakhshaba
Sulfur Letters
Volume 25, Issue 6, 2002
pages 259-261
DOI:10.1080/02786110215846
Sydenhams chorea
- Pupae
- Posts: 97
Casper Struve and Carsten Christophersen
Structural Equilibrium and Ring-Chain Tautomerism of Aqueous Solutions of 4-Aminobutyraldehyde
Heterocycles 2003, 60(08):1907-1914
DOI:10.3987/COM-03-9802
http://anonym.to/?http://www.heterocycles.jp/newlibrary/payments/form/01090/PDF
Abstract
NMR spectroscopy of aqueous solutions of 4-aminobutyraldehyde in the range 0 < pH < 13 established the occurrence of protonated and hydrated amino aldehydes in equilibrium with pyrrolines, and pyrrolinium salts.
Many thanks in advance
No access - RoidRage
For me neither, but a Heterocycles hard copy is in most university libraries. - Enkidu
lugh
- Global Moderator
- Foundress Queen
- Posts: 876
The Synthesis of 4-Chlorobutyric Acid Esters from gamma-Butyrolactone
GOEL, O. P.; SEAMANS, R. E.
Synthesis
1973:538-539
DOI:10.1055/s-1973-22254
Fast and selective oxidation of primary alcohols to aldehydes or to carboxylic acids and of secondary alcohols to ketones mediated by oxoammonium salts under two-phase conditions
Pier Lucio Anelli, Carlo Biffi, Fernando Montanari, Silvio Quici
J Org Chem
1987, 52(12):2559-2562
DOI:10.1021/jo00388a038
gamma-Chlorobutyraldehyde and its Diethyl Acetal
Robert Berner Loftfield
J Am Chem Soc
1951, 73(3):1365-1366
DOI:10.1021/ja01147a519
Improved Fischer Indole Reaction for the Preparation of N,N-Dimethyltryptamines: Synthesis of L-695,894, a Potent 5-HT1D Receptor Agonist
Cheng-yi Chen, Chris H. Senanayake, Timothy J. Bill, Robert D. Larsen, Thomas R. Verhoeven, Paul J. Reider
J Org Chem
1994, 59(13):3738-3741
DOI:10.1021/jo00092a046
are attached
java
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- Posts: 783
Requested by POSEIDON
A NEW TEST FOR DISTINGUISHING THE PRIMARY, SECONDARY AND TERTIARY SATURATED ALCOHOLS
Howard J. Lucas
J. Am. Chem. Soc.
1930, 52 (2), pp 802–804
DOI: 10.1021/ja01365a053
Differentiating between primary, secondary, and tertiary alcohols
Frank O. Ritter
J. Chem. Educ.
1953, 30 (, p 395
DOI: 10.1021/ed030p395
A study of the Lucas test
Richard A. Kjonaas and Bernie A. Riedford
J. Chem. Educ.
1991, 68 (, p 704
DOI: 10.1021/ed068p704
A NEW TEST FOR DISTINGUISHING THE PRIMARY, SECONDARY AND TERTIARY SATURATED ALCOHOLS
Howard J. Lucas
J. Am. Chem. Soc.
1930, 52 (2), pp 802–804
DOI: 10.1021/ja01365a053
Differentiating between primary, secondary, and tertiary alcohols
Frank O. Ritter
J. Chem. Educ.
1953, 30 (, p 395
DOI: 10.1021/ed030p395
A study of the Lucas test
Richard A. Kjonaas and Bernie A. Riedford
J. Chem. Educ.
1991, 68 (, p 704
DOI: 10.1021/ed068p704
lugh
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The full citation:
Efficient and Highly Aldehyde Selective Wacker Oxidation
Peili Teo, Zachary K. Wickens,
Org. Lett. Article ASAP
June 13, 2012
DOI: 10.1021/ol301240g
Abstract
A method for efficient and aldehyde-selective Wacker oxidation of aryl-substituted olefins using PdCl2(MeCN)2, 1,4-benzoquinone, and t-BuOH in air is described. Up to a 96% yield of aldehyde can be obtained, and up to 99% selectivity can be achieved with styrene-related substrates.
and the attached reaction diagram
Efficient and Highly Aldehyde Selective Wacker Oxidation
Peili Teo, Zachary K. Wickens,
Org. Lett. Article ASAP
June 13, 2012
DOI: 10.1021/ol301240g
Abstract
A method for efficient and aldehyde-selective Wacker oxidation of aryl-substituted olefins using PdCl2(MeCN)2, 1,4-benzoquinone, and t-BuOH in air is described. Up to a 96% yield of aldehyde can be obtained, and up to 99% selectivity can be achieved with styrene-related substrates.
and the attached reaction diagram
RoidRage
- Dominant Queen
- Posts: 386
Requested by Embezzler
Efficient and Highly Aldehyde Selective Wacker Oxidation
Peili Teo†‡, Zachary K. Wickens†, Guangbin Dong§, and Robert H. Grubbs*†
Org. Lett., Article ASAP
DOI: 10.1021/ol301240g
Publication Date (Web): June 13, 2012
Comment by requestee:
96% conversion of styrene into phenylacetaldehyde by the looks of it. This mobile device has limited functionality and I am too lazy to type the abstract but it seems to be the case that this approach works with some substituted styrenes. I'm eager to know how and how well
Efficient and Highly Aldehyde Selective Wacker Oxidation
Peili Teo†‡, Zachary K. Wickens†, Guangbin Dong§, and Robert H. Grubbs*†
Org. Lett., Article ASAP
DOI: 10.1021/ol301240g
Publication Date (Web): June 13, 2012
Comment by requestee:
96% conversion of styrene into phenylacetaldehyde by the looks of it. This mobile device has limited functionality and I am too lazy to type the abstract but it seems to be the case that this approach works with some substituted styrenes. I'm eager to know how and how well
RoidRage
- Dominant Queen
- Posts: 386
Requested by Sydenhams Chorea
THE REACTION BETWEEN HIGHLY PHENYLATED COMPOUNDS AND ORGANIC MAGNESIUM COMPOUNDS
E. P. Kohler and E. M. Nygaard
J. Am. Chem. Soc. 1930, 52(10):4128-4139
DOI: 10.1021/ja01373a058
THE REACTION BETWEEN HIGHLY PHENYLATED COMPOUNDS AND ORGANIC MAGNESIUM COMPOUNDS
E. P. Kohler and E. M. Nygaard
J. Am. Chem. Soc. 1930, 52(10):4128-4139
DOI: 10.1021/ja01373a058
Sydenhams chorea
- Pupae
- Posts: 97
Nakamura H, Shimizu M
Comparative study of 1-cyclohexyl-4-(1,2-diphenylethyl)-piperazine and its enantiomorphs on analgesic and othe pharmacological activities in experimental animals
Archives Internationales De Pharmacodynamie Et De Thérapie 1976, 221(1):105-121
PMID: 962421
Abstract
The analgesic activity of (+/-)-1-cycylohexyl-4-(1,2-diphenylethyl)-piperazine (MT-45) was comparable to that of morphine. The activity of the S(+)-isomer was 1.14 to 1.97 times in mice and 1.00 and 1.23 times in rats as potent as MT-45, and 18.3 to 61.6 times as potent as the R(--)isomer, which was approximately comparable to that of Spa. The hyperglycemic and miotic activities of MT-45 and its S(+)-isomer in rabbits were negligible or very low, though they showed potent morphine-like activites. On the other hand, the R(--)-isomer showed no or very weak effects on those, while Spa showed definite effects. These results suggest that the modes of action of MT-45 and its enantiomorphs are partly different from those of morphine and Spa, and it may be concluded that MT-45 belongs to a new series of compounds having a potent analgesic activity.
- Enkidu
Comparative study of 1-cyclohexyl-4-(1,2-diphenylethyl)-piperazine and its enantiomorphs on analgesic and othe pharmacological activities in experimental animals
Archives Internationales De Pharmacodynamie Et De Thérapie 1976, 221(1):105-121
PMID: 962421
Abstract
The analgesic activity of (+/-)-1-cycylohexyl-4-(1,2-diphenylethyl)-piperazine (MT-45) was comparable to that of morphine. The activity of the S(+)-isomer was 1.14 to 1.97 times in mice and 1.00 and 1.23 times in rats as potent as MT-45, and 18.3 to 61.6 times as potent as the R(--)isomer, which was approximately comparable to that of Spa. The hyperglycemic and miotic activities of MT-45 and its S(+)-isomer in rabbits were negligible or very low, though they showed potent morphine-like activites. On the other hand, the R(--)-isomer showed no or very weak effects on those, while Spa showed definite effects. These results suggest that the modes of action of MT-45 and its enantiomorphs are partly different from those of morphine and Spa, and it may be concluded that MT-45 belongs to a new series of compounds having a potent analgesic activity.
- Enkidu
POSEIDON
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- Posts: 116
Studies on 1-substituted 4-(1,2-diphenylethyl)piperazine derivatives and their analgesic activities.
Natsuka K, Nakamura H, Uno H, Umemoto S
Journal of Medicinal Chemistry 1975, 18(12):1240-1244
DOI:10.1021/jm00246a014
PMID:1195277
http://anonym.to/?http://pubs.acs.org/doi/abs/10.1021/jm00246a014
Abstract
The preparation and analgesic activities of a series of the entitled compounds (5-22) and the optical isomers of the 1-cyclohexyl derivative 5 are described. Reactions of N,N-bis(2-chloroethyl)-1,2-diphenylethylamine (3) with ammonia and primary amines gave N-(1,2-diphenylethyl)piperazine (4) and N1-substituted derivatives (5-20, 22), respectively. The alkylation of 4 afforded 12-21. Compounds 5-18 and 22 were also obtained by the reactions of 1,2-diphenylethylamine (23) and N-substituted 2,2'-dichlorodiethylamine. Racemate 5 was resolved with (+)- or (-)-2'-nitrotartranilic acid into its optical isomers [(+)-5 and (-)-5], and the absolute configuration of (+)-5 was determined to be S configuration by the synthesis and optical rotatory dispersion measurements. The most active members in this series of compounds were 5-7, which were approximately as potent as (-)-morphine. In the case of 5, the more potent enantiomer (S)-(+)-5 has the opposite configuration to that of (-)-N,N-dimethyl-1,2-diphenylethylamine (Spa) or (-)-morphine with respect to the (C-9) asymmetric center and belongs to a new series of compounds having potent analgesic activity.
lugh
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Degradation of quaternary ammonium salts. Part VII. New cases of radical migration
Thomas Thomson and Thomas Stevens Stevens
Journal of the Chemical Society (Resumed) 1932, (0):1932-1940
DOI:10.1039/JR9320001932
http://pubs.rsc.org/en/content/articlelanding/1932/jr/jr9320001932
is attached
Thomas Thomson and Thomas Stevens Stevens
Journal of the Chemical Society (Resumed) 1932, (0):1932-1940
DOI:10.1039/JR9320001932
http://pubs.rsc.org/en/content/articlelanding/1932/jr/jr9320001932
is attached