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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lugh
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Requested by Quantum Dude
The oxidation of aldehyde bisulfite adducts to carboxylic acids and their derivatives with dimethylsulfoxide and acetic anhydride
Peter G.M Wuts, Carol L Bergh
Tetrahedron Letters
Volume 27, Issue 34, 1986, Pages 3995–3998
DOI: http://dx.doi.org/10.1016/S0040-4039(00)84893-5
Abstract
Bisulfite adducts which are readily formed from aldehydes are conveniently oxidized to carboxylic acids and derivatives by the action of DMSO/Ac2O followed by quenching with water, an alcohol or an amine
is attached
The oxidation of aldehyde bisulfite adducts to carboxylic acids and their derivatives with dimethylsulfoxide and acetic anhydride
Peter G.M Wuts, Carol L Bergh
Tetrahedron Letters
Volume 27, Issue 34, 1986, Pages 3995–3998
DOI: http://dx.doi.org/10.1016/S0040-4039(00)84893-5
Abstract
Bisulfite adducts which are readily formed from aldehydes are conveniently oxidized to carboxylic acids and derivatives by the action of DMSO/Ac2O followed by quenching with water, an alcohol or an amine
is attached
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Requested by poisoninthestain
The Yeast-Mediated Reduction of Nitrostyrenes in Organic Solvent Systems
R Bak, AF Mcanda, AJ Smallridge and MA Trewhella
Australian Journal of Chemistry
49(11) 1257 - 1260
doi:10.1071/CH9961257
The Yeast-Mediated Reduction of Nitrostyrenes in Organic Solvent Systems
R Bak, AF Mcanda, AJ Smallridge and MA Trewhella
Australian Journal of Chemistry
49(11) 1257 - 1260
doi:10.1071/CH9961257
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Requested by RoidRage
Metabolism of anabolic steroids in man: synthesis and use of reference substances for identification of anabolic steroid metabolites
Willi Schänzer, Manfred Donike
Analytica Chimica Acta
Volume 275, Issues 1–2, 1 April 1993, Pages 23–48
DOI: 10.1016/0003-2670(93)80274-O
Metabolism of anabolic steroids in man: synthesis and use of reference substances for identification of anabolic steroid metabolites
Willi Schänzer, Manfred Donike
Analytica Chimica Acta
Volume 275, Issues 1–2, 1 April 1993, Pages 23–48
DOI: 10.1016/0003-2670(93)80274-O
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Requested by Balkan Boogeyman
Autoxydation von Kohlenwasserstoffen, XXII. Über die Reaktion von ?-Cumyl-hydroperoxyd mit Bleitetraacetat
Heinrich Hock, Heinz Kropf
Chemische Berichte
Volume 91, Issue 8, pages 1681–1687, August 1958
DOI: 10.1002/cber.19580910817
Autoxydation von Kohlenwasserstoffen, XXII. Über die Reaktion von ?-Cumyl-hydroperoxyd mit Bleitetraacetat
Heinrich Hock, Heinz Kropf
Chemische Berichte
Volume 91, Issue 8, pages 1681–1687, August 1958
DOI: 10.1002/cber.19580910817
RoidRage
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Requested by Balkan Boogeyman
Role of Cyclic Tertiary Amine Bioactivation to Reactive Iminium Species: Structure Toxicity Relationship
Peterlin Masic, Lucija
Current Drug Metabolism
Volume 12, Number 1, January 2011 , pp. 35-50(16)
DOI: 10.2174/138920011794520044
Role of Cyclic Tertiary Amine Bioactivation to Reactive Iminium Species: Structure Toxicity Relationship
Peterlin Masic, Lucija
Current Drug Metabolism
Volume 12, Number 1, January 2011 , pp. 35-50(16)
DOI: 10.2174/138920011794520044
lugh
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Requested by Sydenhams chorea:
Structure-activity relations in psychotomimetic phenylalkylamines
F. A. B. Aldous , B. C. Barrass
J. Med. Chem.
1974, 17(10):1100-1111
DOI:10.1021/jm00256a016
http://pubs.acs.org/doi/abs/10.1021/jm00256a016
Structure-activity relations in psychotomimetic phenylalkylamines
F. A. B. Aldous , B. C. Barrass
J. Med. Chem.
1974, 17(10):1100-1111
DOI:10.1021/jm00256a016
http://pubs.acs.org/doi/abs/10.1021/jm00256a016
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Requested by POSEIDON
An elementary laboratory experiment involving the Hofmann rearrangement. The preparation of methylamine hydrochloride from acetamide by means of calcium hypochlorite
C. R. Hauser and W. B. Renfrow
J. Chem. Educ.
1937, 14 (11), p 542
DOI: 10.1021/ed014p542
An elementary laboratory experiment involving the Hofmann rearrangement. The preparation of methylamine hydrochloride from acetamide by means of calcium hypochlorite
C. R. Hauser and W. B. Renfrow
J. Chem. Educ.
1937, 14 (11), p 542
DOI: 10.1021/ed014p542
lugh
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Requested by carl_nnabis
A simple preparation of (R)-(2-cyclopentenyl)acetic acid and (R)-(2-cyclohexenyl)acetic acid using ?-diastereoselective radical cyclization in the presence of Lewis acid
Mayumi Nishida, Hiroshi Hayashi, Yousuke Yamaura
Tetrahedron Letters
Volume 36, Issue 2, 9 January 1995, Pages 269–272
DOI:http://dx.doi.org/10.1016/0040-4039(94)02216-X
is attached
A simple preparation of (R)-(2-cyclopentenyl)acetic acid and (R)-(2-cyclohexenyl)acetic acid using ?-diastereoselective radical cyclization in the presence of Lewis acid
Mayumi Nishida, Hiroshi Hayashi, Yousuke Yamaura
Tetrahedron Letters
Volume 36, Issue 2, 9 January 1995, Pages 269–272
DOI:http://dx.doi.org/10.1016/0040-4039(94)02216-X
is attached
RoidRage
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Requested by carl_nnabis
Synthesis of cannabidiols via alkenylation of cyclohexenyl monoacetate
Kobayashi Y, Takeuchi A, Wang YG.
Org. Lett., 2006, 8 (13), pp 2699–2702
DOI: 10.1021/ol060692h
Synthesis of cannabidiols via alkenylation of cyclohexenyl monoacetate
Kobayashi Y, Takeuchi A, Wang YG.
Org. Lett., 2006, 8 (13), pp 2699–2702
DOI: 10.1021/ol060692h
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Requested by Assyl Fartrate
Iron/Amino Acid Catalyzed Direct N-Alkylation of Amines with Alcohols
Dr. Yingsheng Zhao, Siong Wan Foo, Dr. Susumu Saito
Angewandte Chemie International Edition
2011,Volume 50, Issue 13, pages 3006–3009
DOI: 10.1002/anie.201006660
Abstract
The straightforward N-alkylation using alcohols and iron/amino acid catalysis is described (see scheme). The reaction does not proceed by the conventional “borrowing hydrogen” mechanism, but appears to involve a substitution pathway (SN) at the sp3 carbon atom bearing the hydroxy group of the alcohol. Developing a catalyst that is effective at a near neutral pH was key to the successful N-alkylation.
Selective N-Alkylation of Amines with Alcohols by Using Non-Metal-Based Acid–Base Cooperative Catalysis
Dr. Ya Du, Shunsuke Oishi, Dr. Susumu Saito
Chemistry - A European Journal
2011,Volume 17, Issue 44, pages 12262–12267
DOI: 10.1002/chem.201102446
Abstract
A straightforward method for the selective N-mono- and dialkylation of amines with alcohols by means of non-metal-based catalysis promoted by TAPC is reported (see scheme). Selectivity of the N-mono- and dialkylation, substrate scope and functional-group tolerance are highlighted with respect to each amine (1° and 2°; aromatic and aliphatic) and alcohol (1°, 2° and 3°; benzylic and aliphatic) component.
CuI/H2/NaOH-Catalyzed Cross-Coupling of Two Different Alcohols for Carbon–Carbon Bond Formation: “Borrowing Hydrogen”?
Takashi Miura1, Osamu Kose, Dr. Feng Li, Dr. Sun Kai, Dr. Susumu Saito
Chemistry - A European Journal
2011, Volume 17, Issue 40, pages 11146–11151
DOI: 10.1002/chem.201101752
Abstract
A new method was developed for the cross-coupling of two different alcohols (see scheme). This carbon–carbon bond formation was realized by using a small amount of CuBr (0.05–0.2?mol?%) and NaOH (4–20?mol?%) in the presence of H2 (1?atm), and provides an alternative procedure for longer-chain alcohols. The catalytic cycle was different from those reported to date for the Guerbet reaction involving “borrowing hydrogen
Iron/Amino Acid Catalyzed Direct N-Alkylation of Amines with Alcohols
Dr. Yingsheng Zhao, Siong Wan Foo, Dr. Susumu Saito
Angewandte Chemie International Edition
2011,Volume 50, Issue 13, pages 3006–3009
DOI: 10.1002/anie.201006660
Abstract
The straightforward N-alkylation using alcohols and iron/amino acid catalysis is described (see scheme). The reaction does not proceed by the conventional “borrowing hydrogen” mechanism, but appears to involve a substitution pathway (SN) at the sp3 carbon atom bearing the hydroxy group of the alcohol. Developing a catalyst that is effective at a near neutral pH was key to the successful N-alkylation.
Selective N-Alkylation of Amines with Alcohols by Using Non-Metal-Based Acid–Base Cooperative Catalysis
Dr. Ya Du, Shunsuke Oishi, Dr. Susumu Saito
Chemistry - A European Journal
2011,Volume 17, Issue 44, pages 12262–12267
DOI: 10.1002/chem.201102446
Abstract
A straightforward method for the selective N-mono- and dialkylation of amines with alcohols by means of non-metal-based catalysis promoted by TAPC is reported (see scheme). Selectivity of the N-mono- and dialkylation, substrate scope and functional-group tolerance are highlighted with respect to each amine (1° and 2°; aromatic and aliphatic) and alcohol (1°, 2° and 3°; benzylic and aliphatic) component.
CuI/H2/NaOH-Catalyzed Cross-Coupling of Two Different Alcohols for Carbon–Carbon Bond Formation: “Borrowing Hydrogen”?
Takashi Miura1, Osamu Kose, Dr. Feng Li, Dr. Sun Kai, Dr. Susumu Saito
Chemistry - A European Journal
2011, Volume 17, Issue 40, pages 11146–11151
DOI: 10.1002/chem.201101752
Abstract
A new method was developed for the cross-coupling of two different alcohols (see scheme). This carbon–carbon bond formation was realized by using a small amount of CuBr (0.05–0.2?mol?%) and NaOH (4–20?mol?%) in the presence of H2 (1?atm), and provides an alternative procedure for longer-chain alcohols. The catalytic cycle was different from those reported to date for the Guerbet reaction involving “borrowing hydrogen
lugh
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Requested by POSEIDON:
DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones
Yuhua Zhang † and Chao-Jun Li *†‡
Department of Chemistry, Tulane University, New Orleans, Louisiana 70118, and Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec H3A 2K6, Canada
J. Am. Chem. Soc., 2006, 128 (13), pp 4242–4243
DOI: 10.1021/ja060050p
is attached
DDQ-Mediated Direct Cross-Dehydrogenative-Coupling (CDC) between Benzyl Ethers and Simple Ketones
Yuhua Zhang † and Chao-Jun Li *†‡
Department of Chemistry, Tulane University, New Orleans, Louisiana 70118, and Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec H3A 2K6, Canada
J. Am. Chem. Soc., 2006, 128 (13), pp 4242–4243
DOI: 10.1021/ja060050p
is attached
RoidRage
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Requested by Assyl Fartrate
Stereoselective Construction of Quaternary Carbon Stereocenters via a Semipinacol Rearrangement Strategy
Baomin Wang and Yong Qiang Tu
Acc. Chem. Res., 2011, 44 (11), pp 1207–1222
DOI: 10.1021/ar200082p
Stereoselective Construction of Quaternary Carbon Stereocenters via a Semipinacol Rearrangement Strategy
Baomin Wang and Yong Qiang Tu
Acc. Chem. Res., 2011, 44 (11), pp 1207–1222
DOI: 10.1021/ar200082p
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Requested by Assyl Fartrate
CATALYSIS IN THE CONVERSION OF ALLYL ALCOHOL AND ACROLEIN INTO PROPIONALDEHYDE
Paul E. Weston , Homer Adkins
J. Am. Chem. Soc., 1928, 50 (7), pp 1930–1935
DOI: 10.1021/ja01394a018
Reduction with Alcohols of Cinnamaldehyde to Beta-Phenylpropionaldehyde.
Paul E. Weston , Homer Adkins
J. Am. Chem. Soc., 1929, 51 ( 8 ), pp 2589–2589
DOI: 10.1021/ja01383a501
Use of cyclopropanes and their derivatives in organic synthesis
Henry N. C. Wong , Moon Yuen Hon , Chun Wah Tse , Yu Chi Yip , James Tanko , Tomas Hudlicky
Chem. Rev., 1989, 89 (1), pp 165–198
DOI: 10.1021/cr00091a005
CATALYSIS IN THE CONVERSION OF ALLYL ALCOHOL AND ACROLEIN INTO PROPIONALDEHYDE
Paul E. Weston , Homer Adkins
J. Am. Chem. Soc., 1928, 50 (7), pp 1930–1935
DOI: 10.1021/ja01394a018
Reduction with Alcohols of Cinnamaldehyde to Beta-Phenylpropionaldehyde.
Paul E. Weston , Homer Adkins
J. Am. Chem. Soc., 1929, 51 ( 8 ), pp 2589–2589
DOI: 10.1021/ja01383a501
Use of cyclopropanes and their derivatives in organic synthesis
Henry N. C. Wong , Moon Yuen Hon , Chun Wah Tse , Yu Chi Yip , James Tanko , Tomas Hudlicky
Chem. Rev., 1989, 89 (1), pp 165–198
DOI: 10.1021/cr00091a005
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Requested by Assyl Fartrate
Friedel-Crafts acylation with N-(trifluoroacetyl)-.alpha.-amino acid chlorides. Application to the preparation of .beta.-arylalkylamines and 3-substituted 1,2,3,4-tetrahydroisoquinolines
J. Eric Nordlander , Mark J. Payne
J. Org. Chem.
1984, 49 (22), pp 4107–4111
DOI: 10.1021/jo00196a001
Friedel-Crafts acylation with N-(trifluoroacetyl)-.alpha.-amino acid chlorides. Application to the preparation of .beta.-arylalkylamines and 3-substituted 1,2,3,4-tetrahydroisoquinolines
J. Eric Nordlander , Mark J. Payne
J. Org. Chem.
1984, 49 (22), pp 4107–4111
DOI: 10.1021/jo00196a001
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Requested by Assyl Fartrate
ElectrodimerizationX. Solvation and protonation in the EHD of activated olefins in low acidity media
E. Lamy, L. Nadjo, J.M. Savéant
Journal of Electroanalytical Chemistry and Interfacial Electrochemistry
Volume 50, Issue 1, 10 February 1974, Pages 141–145
http://dx.doi.org/10.1016/S0022-0728(74)80283-4[/color]
ElectrodimerizationX. Solvation and protonation in the EHD of activated olefins in low acidity media
E. Lamy, L. Nadjo, J.M. Savéant
Journal of Electroanalytical Chemistry and Interfacial Electrochemistry
Volume 50, Issue 1, 10 February 1974, Pages 141–145
http://dx.doi.org/10.1016/S0022-0728(74)80283-4[/color]
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Requested by Assyl Fartrate
Hydrolysis of Cinnamaldehyde in Aqueous Solution at Room Temperature Catalyzed by Amino Acids
LuLu Huang, Xingdong Yao, Yongpeng An, Caihua Peng
Advanced Materials Research
(Volumes 512 - 515), Renewable and Sustainable Energy II, 2361-2365
10.4028/www.scientific.net/AMR.512-515.2361
Abstract
The hydrolysis of cinnamaldehyde in aqueous solution catalyzed by amino acids has been investigated. Eight amino acids e.g. glycine, proline etc. have been employed as the small molecular organocatalysts. The effect of reaction time, temperature, buffer concentration on the reaction has been studied. Spectroscopic analysis indicated the reaction product is 3-hydroxy-3-phenylpropanal.
Hydrolysis of Cinnamaldehyde in Aqueous Solution at Room Temperature Catalyzed by Amino Acids
LuLu Huang, Xingdong Yao, Yongpeng An, Caihua Peng
Advanced Materials Research
(Volumes 512 - 515), Renewable and Sustainable Energy II, 2361-2365
10.4028/www.scientific.net/AMR.512-515.2361
Abstract
The hydrolysis of cinnamaldehyde in aqueous solution catalyzed by amino acids has been investigated. Eight amino acids e.g. glycine, proline etc. have been employed as the small molecular organocatalysts. The effect of reaction time, temperature, buffer concentration on the reaction has been studied. Spectroscopic analysis indicated the reaction product is 3-hydroxy-3-phenylpropanal.
java
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Requested by Assyl Fartrate
Reaction of Chloroacetone with Cytisine and d-Pseudoephedrine Alkaloids
O. A. Nurkenov, A. M. Gazaliev, K. M. Turdybekov, A. B. Bukeeva and I. V. Kulakov
Russian Journal of General Chemistry
2003, Volume 73, Number 6, 961-963
DOI: 10.1023/A:1026369205614
Reaction of Chloroacetone with Cytisine and d-Pseudoephedrine Alkaloids
O. A. Nurkenov, A. M. Gazaliev, K. M. Turdybekov, A. B. Bukeeva and I. V. Kulakov
Russian Journal of General Chemistry
2003, Volume 73, Number 6, 961-963
DOI: 10.1023/A:1026369205614
RoidRage
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Requested by EverlastingReign
Zur Geschichte des Cyanurchlorids und der Cyanursäure
Alfred Senier
Berichte der deutschen chemischen Gesellschaft
Volume 19, Issue 1, pages 310–312, Januar–Juni 1886
DOI: 10.1002/cber.18860190175
Zur Geschichte des Cyanurchlorids und der Cyanursäure
Alfred Senier
Berichte der deutschen chemischen Gesellschaft
Volume 19, Issue 1, pages 310–312, Januar–Juni 1886
DOI: 10.1002/cber.18860190175
Pages: 1