Author Topic: Wanted references for August-September 2012 (Read 439 times)

java · « **on:** August 04, 2012, 02:25:16 AM »

Quote from: Enkidu on May 03, 2012, 06:30:37 AM

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.

lugh · « **Reply #1 on:** August 18, 2012, 09:02:39 AM »

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

java · « **Reply #2 on:** August 22, 2012, 09:47:26 PM »

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

java · « **Reply #3 on:** August 23, 2012, 03:34:06 AM »

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

java · « **Reply #4 on:** August 24, 2012, 03:49:08 AM »

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

RoidRage · « **Reply #5 on:** August 25, 2012, 01:39:15 AM »

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

lugh · « **Reply #6 on:** August 29, 2012, 02:16:49 AM »

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

java · « **Reply #7 on:** September 08, 2012, 09:13:30 PM »

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

lugh · « **Reply #8 on:** September 11, 2012, 10:50:57 PM »

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

RoidRage · « **Reply #9 on:** September 11, 2012, 11:13:28 PM »

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

java · « **Reply #10 on:** September 23, 2012, 01:17:34 PM »

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

lugh · « **Reply #11 on:** September 27, 2012, 11:59:32 PM »

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

RoidRage · « **Reply #12 on:** September 28, 2012, 12:11:04 AM »

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

Polonium · « **Reply #13 on:** September 28, 2012, 09:43:33 AM »

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

java · « **Reply #14 on:** September 29, 2012, 01:47:25 PM »

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

java · « **Reply #15 on:** September 29, 2012, 06:46:34 PM »

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]

java · « **Reply #16 on:** September 29, 2012, 06:48:11 PM »

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.

java · « **Reply #17 on:** September 30, 2012, 10:17:52 PM »

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

RoidRage · « **Reply #18 on:** October 03, 2012, 02:17:32 AM »

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

Author Topic: Wanted references for August-September 2012 (Read 439 times)

java

Wanted references for August-September 2012

lugh

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

RoidRage

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lugh

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

lugh

Re: Wanted references for August 2012

RoidRage

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

lugh

Re: Wanted references for August 2012

RoidRage

Re: Wanted references for August 2012

Polonium

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

java

Re: Wanted references for August 2012

RoidRage

Re: Wanted references for August 2012