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.
Pages: 1
java
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fishinabottle
- Subordinate Wasp
- Posts: 129
My interest was stirred by an article you posted at SCM so see, it's all your fault!
Production of phenylacetic acid by the liquid phase oxidation of acetophenone with sulphur in the presence of aqueous ammonia
Jitendra K. Jain, Sampatraj B. Chandalia
Journal of Applied Chemistry and Biotechnology, Volume 24, Issue 3, pages 105–112, March 1974
DOI: 10.1002/jctb.2720240302
.
regards
/ORG
Production of phenylacetic acid by the liquid phase oxidation of acetophenone with sulphur in the presence of aqueous ammonia
Jitendra K. Jain, Sampatraj B. Chandalia
Journal of Applied Chemistry and Biotechnology, Volume 24, Issue 3, pages 105–112, March 1974
DOI: 10.1002/jctb.2720240302
.
regards
/ORG
lugh
- Global Moderator
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- Posts: 876
Quote
I could not find title or DOI, not even locate the origin and homepage of the journal. Anyways it is about a Willgerodt like microwave driven styrene transformation.
That article was scanned upon the request of the mad moose many years ago The apparent reason that the doi is hard to find is that publishers are trying to sell abstracts in addition to full articles:
Microwave assisted Willgerodt-Kindler reaction of styrenes
Moghaddam, Firouz Matloubi; Ghaffarzadeh, Mohammad; Dakamin, Mohammad G.
Journal of Chemical Research
Volume 2000, Number 5, 1 May 2000 , pp. 228-229(2)
DOI: http://dx.doi.org/10.3184/030823400103167084
Abstract
Styrenes are efficiently transformed to thioamides via the Willgerodt-Kindler reaction under microwave irradiation.
The article has been available at the Collective for many years:
https://the-collective.ws/forum/index.php?topic=13920.msg142761#msg142761
The end results from the effort applied
RoidRage
- Dominant Queen
- Posts: 386
Requested by POSEIDON
Über Bromierungen mit Dibromoisocyanursäure unter ionischen Bedingungen, 1. Mitt.: Monobromierungen
W. Gottardi
MONATSHEFTE FÜR CHEMIE / CHEMICAL MONTHLY
Volume 99, Number 2 (1968), 815-822, DOI: 10.1007/BF00901238
http://www.springerlink.com/content/k77m14682vm382q8/
Über Bromierungen mit Dibromoisocyanursäure unter ionischen Bedingungen, 1. Mitt.: Monobromierungen
W. Gottardi
MONATSHEFTE FÜR CHEMIE / CHEMICAL MONTHLY
Volume 99, Number 2 (1968), 815-822, DOI: 10.1007/BF00901238
http://www.springerlink.com/content/k77m14682vm382q8/
java
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Requested by POSEIDON
ChemInform Abstract: A New Radical Way to N,N-Dimethylaniline Hydroperoxide (DMAHP) and Its Application in Organic Synthesis.
Yi Xu, Shi Lei Zhang, Wen Hu Duan
ChemInform
Volume 39, Issue 18, page no, April 29, 2008
DOI: 10.1002/chin.200818138
http://onlinelibrary.wiley.com/doi/10.1002/chin.200818138/abstract
.........points to this,
A new radical way to N,N-dimethylaniline hydroperoxide (DMAHP) and its application in organic synthesis
Yi Xu, Shi Lei Zhang, Wen Hu Duan
Chinese Chemical Letters
Volume 18, Issue 7, July 2007, Pages 807-810
http://dx.doi.org/10.1016/j.cclet.2007.05.036
ChemInform Abstract: A New Radical Way to N,N-Dimethylaniline Hydroperoxide (DMAHP) and Its Application in Organic Synthesis.
Yi Xu, Shi Lei Zhang, Wen Hu Duan
ChemInform
Volume 39, Issue 18, page no, April 29, 2008
DOI: 10.1002/chin.200818138
http://onlinelibrary.wiley.com/doi/10.1002/chin.200818138/abstract
.........points to this,
A new radical way to N,N-dimethylaniline hydroperoxide (DMAHP) and its application in organic synthesis
Yi Xu, Shi Lei Zhang, Wen Hu Duan
Chinese Chemical Letters
Volume 18, Issue 7, July 2007, Pages 807-810
http://dx.doi.org/10.1016/j.cclet.2007.05.036
RoidRage
- Dominant Queen
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Requested by POSEIDON
Über die Reaktion von Brom mit Alkalicyanuraten
INORGANIC, STRUCTURAL AND PHYSICAL CHEMISTRY
W. Gottardi
MONATSHEFTE FÜR CHEMIE / CHEMICAL MONTHLY
Volume 98, Number 2 (1967), 507-512, DOI: 10.1007/BF00899972
http://www.springerlink.com/content/l285k37466666450/
Über die Reaktion von Brom mit Alkalicyanuraten
INORGANIC, STRUCTURAL AND PHYSICAL CHEMISTRY
W. Gottardi
MONATSHEFTE FÜR CHEMIE / CHEMICAL MONTHLY
Volume 98, Number 2 (1967), 507-512, DOI: 10.1007/BF00899972
http://www.springerlink.com/content/l285k37466666450/
java
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Requested by POSEIDON
Characterization of the synthesis of N,N-dimethyltryptamine by reductive amination using gas chromatography ion trap mass spectrometry
Simon D. Brandt1,*, Sharon A. Moore1, Sally Freeman2, Abu B. Kanu3
Drug Testing and Analysis
Volume 2, Issue 7, pages 330–338, July 2010
DOI: 10.1002/dta.142
Adulterants in illicit drugs: a review of empirical evidence
Claire Cole1, Lisa Jones1, Jim McVeigh1,*, Andrew Kicman2, Qutub Syed3, Mark Bellis1
Drug Testing and Analysis
Volume 3, Issue 2, pages 89–96, February 2011
DOI: 10.1002/dta.220
Methylamphetamine synthesis: Does an alteration in synthesis conditions affect the ?13C, ?15N and ?2H stable isotope ratio values of the product?
Helen Salouros*, Michael Collins*, Adam Cawley, Mitchell Longworth
Drug Testing and Analysis
Volume 4, Issue 5, pages 330–336, May 2012
DOI: 10.1002/dta.321
GC-MS and GC-IRD studies on brominated dimethoxyamphetamines: Regioisomers related to 4-Br-2,5-DMA (DOB)
Hadir M. Maher1, Tamer Awad2,3, Jack DeRuiter3, C. Randall Clark3,*
Drug Testing and Analysis
Special Issue: Psychedelic Substances
Volume 4, Issue 7-8, pages 591–600, July-August 2012
DOI: 10.1002/dta.409
Characterization of the synthesis of N,N-dimethyltryptamine by reductive amination using gas chromatography ion trap mass spectrometry
Simon D. Brandt1,*, Sharon A. Moore1, Sally Freeman2, Abu B. Kanu3
Drug Testing and Analysis
Volume 2, Issue 7, pages 330–338, July 2010
DOI: 10.1002/dta.142
Adulterants in illicit drugs: a review of empirical evidence
Claire Cole1, Lisa Jones1, Jim McVeigh1,*, Andrew Kicman2, Qutub Syed3, Mark Bellis1
Drug Testing and Analysis
Volume 3, Issue 2, pages 89–96, February 2011
DOI: 10.1002/dta.220
Methylamphetamine synthesis: Does an alteration in synthesis conditions affect the ?13C, ?15N and ?2H stable isotope ratio values of the product?
Helen Salouros*, Michael Collins*, Adam Cawley, Mitchell Longworth
Drug Testing and Analysis
Volume 4, Issue 5, pages 330–336, May 2012
DOI: 10.1002/dta.321
GC-MS and GC-IRD studies on brominated dimethoxyamphetamines: Regioisomers related to 4-Br-2,5-DMA (DOB)
Hadir M. Maher1, Tamer Awad2,3, Jack DeRuiter3, C. Randall Clark3,*
Drug Testing and Analysis
Special Issue: Psychedelic Substances
Volume 4, Issue 7-8, pages 591–600, July-August 2012
DOI: 10.1002/dta.409
Polonium
- Pupae
- Posts: 70
117. Reduction by dissolving metals. Part I
Arthur J. Birch
J. Chem. Soc., 1944, 430-436
DOI: 10.1039/JR9440000430
Arthur J. Birch
J. Chem. Soc., 1944, 430-436
DOI: 10.1039/JR9440000430
java
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- Foundress Queen
- Posts: 783
Requested by no_dream
Studies on chemical structure and analgetic activity of phenyl substituted aminomethylcyclohexanoles | UNTERSUCHUNGEN ZUR CHEMISCHEN STRUKTUR UND ANALGETISCHEN WIRKUNG VON PHENYLSUBSTITUIERTEN AMINOMETHYLCYCLOHEXANOLEN
Flick, K.; Frankus, E.; Friderichs, E.
Arzneimittel-Forsch./Drug.Res.
1978, 28(I), Heft 1a:p. 107-113
Studies on chemical structure and analgetic activity of phenyl substituted aminomethylcyclohexanoles | UNTERSUCHUNGEN ZUR CHEMISCHEN STRUKTUR UND ANALGETISCHEN WIRKUNG VON PHENYLSUBSTITUIERTEN AMINOMETHYLCYCLOHEXANOLEN
Flick, K.; Frankus, E.; Friderichs, E.
Arzneimittel-Forsch./Drug.Res.
1978, 28(I), Heft 1a:p. 107-113
java
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Requested by POSEIDON
Biomass production, total protein, chlorophylls, lipids and fatty acids of freshwater green and blue-green algae under different nitrogen regimes.
Piorreck M, Baasch K, Pohl P.
Phytochemistry
1984; 23(2): 207-216.
http://dx.doi.org/10.1016/S0031-9422(00)80304-0
Biomass production, total protein, chlorophylls, lipids and fatty acids of freshwater green and blue-green algae under different nitrogen regimes.
Piorreck M, Baasch K, Pohl P.
Phytochemistry
1984; 23(2): 207-216.
http://dx.doi.org/10.1016/S0031-9422(00)80304-0
java
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Requested by POSEIDON
Safrole, the Main Component of the Essential Oil from Piper auritum of Panama
Mahabir P. Gupta , Tomás D. Arias , Norris H. Williams , R. Bos , D. H. E. Tattje
J. Nat. Prod.
1985, 48 (2), pp 330–330
DOI: 10.1021/np50038a026
Safrole, the Main Component of the Essential Oil from Piper auritum of Panama
Mahabir P. Gupta , Tomás D. Arias , Norris H. Williams , R. Bos , D. H. E. Tattje
J. Nat. Prod.
1985, 48 (2), pp 330–330
DOI: 10.1021/np50038a026
java
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Requested by Assyl Fartrate
New Entries in Lewis Acid-Lewis Base Bifunctional Asymmetric Catalyst: Catalytic Enantioselective Reissert Reaction of Pyridine Derivatives
Eiko Ichikawa, Masato Suzuki, Kazuo Yabu, Matthias Albert, Motomu Kanai, and Masakatsu Shibasaki
J. Am. Chem. Soc.
2004, 126 (38), pp 11808–11809
DOI: 10.1021/ja045966f
Synthesis of Pyridine and Dihydropyridine Derivatives by Regio- and Stereoselective Addition to N-Activated Pyridines
James A. Bull, James J. Mousseau, Guillaume Pelletier, and André B. Charette
Chem. Rev.
2012, 112 (5), pp 2642–2713
DOI: 10.1021/cr200251d
Chemistry and Pharmacology of 4-Alkoxy-piperidines Related to Reversed Esters of Pethidine
A. F. Casy , A. H. Beckett , G. H. Hall , D. K. Vallance
J. Med. Chem.
1961, 4 (3), pp 535–551
DOI: 10.1021/jm50019a012
Weakly Basic Analogues of Potent Analgesics
A. H. Beckett , J. V. Greenhill
J. Med. Chem.
1961, 4 (3), pp 423–436
DOI: 10.1021/jm50019a001
General method for the synthesis of bridged indole alkaloids. Nucleophilic addition of indoleacetic ester enolates to N-alkylpyridinium salts
M. Lluisa Bennasar , Mercedes Alvarez , Rodolfo Lavilla , Ester Zulaica , Joan Bosch
J. Org. Chem.
1990, 55 (4), pp 1156–1168
DOI: 10.1021/jo00291a013
New Entries in Lewis Acid-Lewis Base Bifunctional Asymmetric Catalyst: Catalytic Enantioselective Reissert Reaction of Pyridine Derivatives
Eiko Ichikawa, Masato Suzuki, Kazuo Yabu, Matthias Albert, Motomu Kanai, and Masakatsu Shibasaki
J. Am. Chem. Soc.
2004, 126 (38), pp 11808–11809
DOI: 10.1021/ja045966f
Synthesis of Pyridine and Dihydropyridine Derivatives by Regio- and Stereoselective Addition to N-Activated Pyridines
James A. Bull, James J. Mousseau, Guillaume Pelletier, and André B. Charette
Chem. Rev.
2012, 112 (5), pp 2642–2713
DOI: 10.1021/cr200251d
Chemistry and Pharmacology of 4-Alkoxy-piperidines Related to Reversed Esters of Pethidine
A. F. Casy , A. H. Beckett , G. H. Hall , D. K. Vallance
J. Med. Chem.
1961, 4 (3), pp 535–551
DOI: 10.1021/jm50019a012
Weakly Basic Analogues of Potent Analgesics
A. H. Beckett , J. V. Greenhill
J. Med. Chem.
1961, 4 (3), pp 423–436
DOI: 10.1021/jm50019a001
General method for the synthesis of bridged indole alkaloids. Nucleophilic addition of indoleacetic ester enolates to N-alkylpyridinium salts
M. Lluisa Bennasar , Mercedes Alvarez , Rodolfo Lavilla , Ester Zulaica , Joan Bosch
J. Org. Chem.
1990, 55 (4), pp 1156–1168
DOI: 10.1021/jo00291a013
java
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Requested by Assyl Fartrate
Title: Synthesis and characterization of meperidine analogs at the P-glycoprotein efflux transporter
Authors: Mercer, Susan L.
Advisors: Coop, Andrew
Date: 2008
Description: University of Maryland, Baltimore. Pharmaceutical Sciences. Ph.D. 2008
Type: dissertation
----------------------------------------------------------------------------------
Title: Opioid analgesics with reduced tolerance
Authors: Cunningham, Christopher W.
Advisors: Coop, Andrew
Date: 2008
Description: University of Maryland, Baltimore. Pharmaceutical Sciences. Ph.D. 2008
Type: dissertation
......this one has to be bought....java
http://www.docstoc.com/docs/47021879/Opioid-analgesics-with-reduced-tolerance
Title: Synthesis and characterization of meperidine analogs at the P-glycoprotein efflux transporter
Authors: Mercer, Susan L.
Advisors: Coop, Andrew
Date: 2008
Description: University of Maryland, Baltimore. Pharmaceutical Sciences. Ph.D. 2008
Type: dissertation
----------------------------------------------------------------------------------
Title: Opioid analgesics with reduced tolerance
Authors: Cunningham, Christopher W.
Advisors: Coop, Andrew
Date: 2008
Description: University of Maryland, Baltimore. Pharmaceutical Sciences. Ph.D. 2008
Type: dissertation
......this one has to be bought....java
http://www.docstoc.com/docs/47021879/Opioid-analgesics-with-reduced-tolerance
java
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Requested by Assyl Fartrate
Opioids and efflux transporters. Part 1: P-Glycoprotein substrate activity of N-substituted analogs of meperidine
Susan L. Mercer, Hazem E. Hassan, Christopher W. Cunningham, Natalie D. Eddington, Andrew Coop
Bioorganic & Medicinal Chemistry Letters
Volume 17, Issue 5, 1 March 2007, Pages 1160–1162
http://dx.doi.org/10.1016/j.bmcl.2006.12.042
Opioids and Efflux Transporters. Part 2: P-Glycoprotein Substrate Activity of 3- and 6-Substituted Morphine Analogs
Christopher W. Cunningham, Susan L. Mercer, Hazem E. Hassan, John R. Traynor, Natalie D. Eddington and Andrew Coop
J. Med. Chem.
2008, 51 (7), pp 2316–2320
DOI: 10.1021/jm701457j
Opioids and efflux transporters. Part 3: P-glycoprotein substrate activity of 3-hydroxyl addition to meperidine analogs
Susan L. Mercer, Christopher W. Cunningham, Natalie D. Eddington, Andrew Coop
Bioorganic & Medicinal Chemistry Letters
Volume 18, Issue 12, 15 June 2008, Pages 3638–3640
http://dx.doi.org/10.1016/j.bmcl.2008.04.046
Evaluation of the P-glycoprotein (Abcb1) affinity status of a series of morphine analogs: Comparative study with meperidine analogs to identify opioids with minimal P-glycoprotein interactions
Hazem E. Hassan, Susan L. Mercer, Christopher W. Cunningham, Andrew Coop, Natalie D. Eddington
International Journal of Pharmaceutics
Volume 375, Issues 1–2, 22 June 2009, Pages 48–54
http://dx.doi.org/10.1016/j.bmcl.2008.04.046
Opioids and efflux transporters. Part 1: P-Glycoprotein substrate activity of N-substituted analogs of meperidine
Susan L. Mercer, Hazem E. Hassan, Christopher W. Cunningham, Natalie D. Eddington, Andrew Coop
Bioorganic & Medicinal Chemistry Letters
Volume 17, Issue 5, 1 March 2007, Pages 1160–1162
http://dx.doi.org/10.1016/j.bmcl.2006.12.042
Opioids and Efflux Transporters. Part 2: P-Glycoprotein Substrate Activity of 3- and 6-Substituted Morphine Analogs
Christopher W. Cunningham, Susan L. Mercer, Hazem E. Hassan, John R. Traynor, Natalie D. Eddington and Andrew Coop
J. Med. Chem.
2008, 51 (7), pp 2316–2320
DOI: 10.1021/jm701457j
Opioids and efflux transporters. Part 3: P-glycoprotein substrate activity of 3-hydroxyl addition to meperidine analogs
Susan L. Mercer, Christopher W. Cunningham, Natalie D. Eddington, Andrew Coop
Bioorganic & Medicinal Chemistry Letters
Volume 18, Issue 12, 15 June 2008, Pages 3638–3640
http://dx.doi.org/10.1016/j.bmcl.2008.04.046
Evaluation of the P-glycoprotein (Abcb1) affinity status of a series of morphine analogs: Comparative study with meperidine analogs to identify opioids with minimal P-glycoprotein interactions
Hazem E. Hassan, Susan L. Mercer, Christopher W. Cunningham, Andrew Coop, Natalie D. Eddington
International Journal of Pharmaceutics
Volume 375, Issues 1–2, 22 June 2009, Pages 48–54
http://dx.doi.org/10.1016/j.bmcl.2008.04.046
java
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Requested by Assyl Fartrate
Structure-activity study of the mechanism of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity. I. Evaluation of the biological activity of MPTP analogs.
S K Youngster, P K Sonsalla, B A Sieber and R E Heikkila
J Pharmacol Exp Ther
June 1989 vol. 249 no. 3 820-828
DOI: Unknown
Abstract:
Several analogs of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) were synthesized and compared to MPTP for their ability to be oxidized by monoamine oxidase (MAO) and for their ability to cause nigrostriatal dopaminergic neurotoxicity in mice. Most of the compounds were oxidized by mouse brain MAO, either predominantly by the B-form or by both the A- and B-forms. The MAO-catalyzed oxidation of all of the MAO substrates resulted in the formation of dihydropyridinium intermediates which, in turn, except for the dihydropyridinium of 1-methyl-4-benzyl-1,2,3,6-tetrahydropyridine, formed pyridinium species as the final oxidation product. Nine analogs were found to be neurotoxic; all were oxidized by MAO to pyridinium compounds.
Structure-activity study of the mechanism of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity. I. Evaluation of the biological activity of MPTP analogs.
S K Youngster, P K Sonsalla, B A Sieber and R E Heikkila
J Pharmacol Exp Ther
June 1989 vol. 249 no. 3 820-828
DOI: Unknown
Abstract:
Several analogs of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) were synthesized and compared to MPTP for their ability to be oxidized by monoamine oxidase (MAO) and for their ability to cause nigrostriatal dopaminergic neurotoxicity in mice. Most of the compounds were oxidized by mouse brain MAO, either predominantly by the B-form or by both the A- and B-forms. The MAO-catalyzed oxidation of all of the MAO substrates resulted in the formation of dihydropyridinium intermediates which, in turn, except for the dihydropyridinium of 1-methyl-4-benzyl-1,2,3,6-tetrahydropyridine, formed pyridinium species as the final oxidation product. Nine analogs were found to be neurotoxic; all were oxidized by MAO to pyridinium compounds.
Pages: 1