Author Topic: 2011 Reference Requests (Read 3668 times)

java · « **Reply #120 on:** June 14, 2011, 12:22:40 AM »

Quote from: POSEIDON on June 13, 2011, 12:20:04 AM

Please this article , thanks in advance

Journal of the Society of Chemical Industry
Volume 27, Issue 10, pages 483–485, 30 May 1908
The manufacture of sodium nitrite
Gilbert T. Morgan D.SC.
Article first published online: 30 MAY 2007
DOI: 10.1002/jctb.5000271004
http://onlinelibrary.wiley.com/doi/10.1002/jctb.5000271004/abstract

xxxxx · « **Reply #121 on:** June 14, 2011, 02:12:46 PM »

A Convenient Synthesis of 3,4-Dimethoxy-5-hydroxybenzaldehyde
James E. Ellisa; Steven R. Lengera
Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 28, Issue 9, 1998, Pages 1517 - 1524
DOI: 10.1080/00397919808006854
http://www.informaworld.com/smpp/content~db=all?content=10.1080/00397919808006854

RoidRage · « **Reply #122 on:** June 16, 2011, 02:09:38 AM »

Quote from: poorfish on June 16, 2011, 01:30:05 AM

Copper-mediated oxidative DNA damage induced by eugenol: possible involvement of O-demethylation

Mutation Research/Genetic Toxicology and Environmental Mutagenesis
Volume 565, Issue 1, 31 December 2004, Pages 35-44

Authors: Katsuhisa Sakano, Yuji Inagaki, Shinji Oikawa, Yusuke Hiraku and Shosuke Kawanishi

java · « **Reply #123 on:** June 28, 2011, 03:46:08 PM »

Quote from: no1uno on June 15, 2011, 02:38:57 PM

Chlorination of Ketones with Trichloroisocyanuric Acid

Synthetic Communications
Volume 15, Issue 5, 1985, Pages 385 - 392
Authors: Gene A. Hiegela; Kim B. Peytona
DOI: 10.1080/00397918508063816

Abstract
Trichloroisocyanuric acid is an effective reagent for the chlorination of ketones in the alpha position.

I

java · « **Reply #124 on:** June 28, 2011, 03:47:39 PM »

Quote from: beanhead on June 24, 2011, 04:55:24 PM

Some pharmacological studies with 14-cinnamoyloxycodeinone
W. R. Buckett,†
Article first published online: 12 APR 2011

DOI: 10.1111/j.2042-7158.1965.tb07602.x

http://onlinelibrary.wiley.com/doi/10.1111/j.2042-7158.1965.tb07602.x/abstract

This compound means gold if it's pharmacology is worth anything at all; 100x times the potency is great but if it's halflife is too short I think i'll just let it be...

Cheers

java · « **Reply #125 on:** June 28, 2011, 03:49:08 PM »

Quote from: EverlastingReign on June 03, 2011, 04:06:21 PM

Hi

I request:

Halogen compounds related to the reversed esters of pethidine

Journal of Pharmacy and Pharmacology
Volume 16, Issue 2, pages 72–78, February 1964
DOI: 10.1111/j.2042-7158.1964.tb07424.x

Regards.

RoidRage · « **Reply #126 on:** July 01, 2011, 03:13:53 AM »

Quote from: Terror on July 01, 2011, 12:45:04 AM

Palladium-Catalyzed Oxidative Rearrangement of Diaryl Alkenyl Carbinols to ?,?-Diaryl ?,?-Unsaturated Ketones
3-Haloquinolines by Friedlnder Reaction of ?-Haloketones
Total Synthesis of (±)-Trigonoliimine C via Oxidative Rearrangement of an Unsymmetrical Bis-Tryptamine

Palladium-Catalyzed Oxidative Rearrangement of Diaryl Alkenyl Carbinols to ?,?-Diaryl ?,?-Unsaturated Ketones
David Rosa Arturo Orellana
Org. Lett. , Articles ASAP (As Soon As Publishable)
2011

3-Haloquinolines by Friedlnder Reaction of ?-Haloketones
Sergey V. Ryabukhin Vasiliy S. Naumchik; Andrey S. Plaskon; Oleksandr O. Grygorenko; Andrey A. Tolmachev
J. Org. Chem. , Articles ASAP (As Soon As Publishable)
2011

Total Synthesis of (±)-Trigonoliimine C via Oxidative Rearrangement of an Unsymmetrical Bis-Tryptamine
Xiangbing Qi Hongli Bao; Uttam K. Tambar
J. Am. Chem. Soc. , 2011, 133 (26), pp 10050–10053
2011

RoidRage · « **Reply #127 on:** July 08, 2011, 02:29:39 AM »

Quote from: Sedit on July 08, 2011, 01:59:51 AM

doi:10.1016/j.ejop.2007.07.001

Phylogenetic analyses of the dinoflagellate Noctiluca scintillans based on ?-tubulin and Hsp90 genes

Abstract
Quote
The noctilucid dinoflagellate Noctiluca scintillans is an unarmed heterotrophic protist that inhabits the world's oceans and is sometimes responsible for harmful red tides. The phylogenetic position of the noctilucids has been widely disputed because of two alternative views based on morphological characters and phylogenetic analyses using SSU rDNA. Specifically, noctilucids are either placed in a basal position within the dinoflagellates or they are seen as evolutionarily recent derivations descended from unarmored dinoflagellates in the order Gymnodiniales. Thus, the precise relationship of noctilucids to other dinoflagellates is still uncertain. In this study, we isolated ?-tubulin and heat shock protein 90 genes from N. scintillans to examine this relationship further. The deduced amino acid sequences share commonly substituted amino acids and a deletion with other dinoflagellates, but not with Perkinsus marinus or other alveolates. Although Hsp90 analysis did not give robust support, ?-tubulin analysis including an AU test, as well as combined analysis of these two amino acid sequences showed that N. scintillans is the next earliest branch after Oxyrrhis marina, within the dinoflagellates. Given the phylogenetic position of N. scintillans, its extremely specialized diploid trophont, and the primitive dinoflagellate-like characteristics of its haploid zoospore, we propose that noctilucids are a possible evolutionary link between ancestral diploid dinoflagellates and haploid core dinoflagellates. This implies that the transition from diploidy to haploidy in trophonts probably occurred via neoteny of a noctilucid-like zoospore.

Keywords: Alveolates; Dinoflagellates; Noctilucae; Zoospore; Ploidy change; Phylogeny
Article Outline

Abstract link: http://www.sciencedirect.com/science/article/pii/S0932473907000442#secx3

java · « **Reply #128 on:** July 08, 2011, 05:07:17 AM »

Quote from: Enkidu on July 06, 2011, 05:16:14 AM

Joong-Youn Shim, Elizabeth R. Collantes, William J. Welsh, and Allyn C. Howlett
"Unified Pharmacophoric Model for Cannabinoids and Aminoalkylindoles Derived from Molecular Superimposition of CB1 Cannabinoid Receptor Agonists CP55244 and WIN55212-2"
Rational Drug Design 1999, Chapter 11, pp.165-184
DOI: 10.1021/bk-1999-0719.ch011

http://ifile.it/6b4axr5

Note: sorry i forgot to add the link to the whole book where your inquiry can be found....java

Enkidu · « **Reply #129 on:** July 13, 2011, 12:00:01 AM »

If you're interested in zinc borohydride, be sure to check out this review: http://www.erowid.org/archive/rhodium/pdf/zinc.borohydride.pdf

Quote from: antibody2 on July 12, 2011, 01:56:26 PM

Unusual Reactivity of Zinc Borohydride - Reduction of Amides to Amines
Narasimhan, S.; Madhavan,
Synthetic Communications
1997, Volume 27, Issue 3, pages 391-394
DOI:10.1080/00397919708006038
http://www.tandfonline.com/doi/abs/10.1080/00397919708006038

java · « **Reply #130 on:** July 18, 2011, 02:54:32 AM »

Characteristics of the saprophytic reference strain FA of Claviceps paspali
A. ?i?icová, V. Pokorný and Z. ?ehá?ek
Folia Microbiologica
Volume 31, Number 1, 32-43,
DOI: 10.1007/BF02928677

java · « **Reply #131 on:** July 19, 2011, 12:13:33 PM »

Aqueous extraction of sugarcane bagasse hemicellulose and production of xylose syrup

M. Saska & E. Ozer

Biotechnology and Bioengineering
Vol.45(6) 1995 pp.517–523
DOI: 10.1002/bit.260450609

Abstract

At the optimum level of severity, the aqueous extraction of sugarcane bagasse, an abundant agricultural resdue, gave, depending on the degree of comminution, 60% to 89% yield of xylose, most of it in the form of a water soluble xylan. A process for producing xylose-rich syrups was conceived and tested, consisting of aqueous extraction, acid hydrolysis of the concentrated aqueous extract centrifugal clarification of the hydrolysate, and recovery of the acid by continuous ion exclusion. The cost estimate indicates operating costs on the order of $0.12 to $0.15/kg xylose, in the form of xylose-rich molasses.

RoidRage · « **Reply #132 on:** July 21, 2011, 12:50:41 AM »

Quote from: oldguy on July 21, 2011, 12:08:18 AM

Stereospecificity of the Baeyer-Villiger Rearrangement
Kurt Mislow and Joseph Brenner
Journal of the American Chemical Society
1953, 75 (10), pp 2318–2322
DOI: 10.1021/ja01106a009

RoidRage · « **Reply #133 on:** July 29, 2011, 07:22:25 PM »

Ozonolysis of alkenes and study of reactions of polyfunctional compounds
G. Yu. Ishmuratov, A. Kh. Shayakhmetova
Russian Journal of Organic Chemistry
Volume 43, Number 8, 1114-1119, DOI: 10.1134/S1070428007080039

java · « **Reply #134 on:** August 01, 2011, 02:32:06 PM »

Please provide as much information for our request so we may use our limited time wisely and not searching for the article link...

.......you know the routine,

title of article
author
name of journal
year, volume, pages
doi

......this important so the people assisting you will not waste their time looking for the reference and just use their time acquiring them you......java

JustDreaming · « **Reply #135 on:** August 04, 2011, 05:00:01 AM »

Olivetol: Constituent of lichen Evernia prunastri Ach. or "oakmoss"
Hassuni I, Razxouk H.
Physical and Chemical News 26: 98–103.
2005

This one is interesting because I have found another source claiming it does not contain any after a GC-MS analysis.

Hopefully this is sufficient information. Thank you for finding these

.

Try to enclose the link to the journal and the doi....it helps when looking for it ...since i have so little time ....something you can do to save time....java

P.S. I found this info which you can meal with until your study is found....

Ethnolichenology of the World

http://web.uvic.ca/~stucraw/part1.html

java · « **Reply #136 on:** August 13, 2011, 02:48:23 AM »

Requested by dingbow

A Versatile Modification of the Hofmann Rearrangement
Radlick and Brown
Synthesis
1974, 290-292
doi/10.1055/s-1974-23298

reDEEMed · « **Reply #137 on:** August 13, 2011, 07:21:27 PM »

Fabric softeners as phase transfer catalyst in organic synthesis
Albert W. M. Lee and W. C. Yip
J. Chem. Educ.
1991, 68 (1), p 69
DOI: 10.1021/ed068p69

java · « **Reply #138 on:** August 16, 2011, 04:31:56 AM »

Requested by OoBYCoO

Submerged culture growth of edible mushrooms on waste sulphite liquors.
Kosaric, N., Leduy, A. and Zajic, J. E.
The Canadian Journal of Chemical Engineering
1973, 51: 186–190.
doi: 10.1002/cjce.5450510208

java · « **Reply #139 on:** August 21, 2011, 04:29:13 PM »

Requested by POSEIDON

Some new psychoactive substances: Precursor chemicals and synthesis-driven end-products
Michael Collins
Drug Testing and Analysis
Special Issue: New Psychoactive Substances
2011,Volume 3, Issue 7-8, pages 404–416
DOI: 10.1002/dta.315

The emergence and analysis of synthetic cannabinoids
Simon Hudson1,*,John Ramsey
Drug Testing and Analysis
Special Issue: New Psychoactive Substances
2011, Volume 3, Issue 7-8, pages 466–478
DOI: 10.1002/dta.268

Author Topic: 2011 Reference Requests (Read 3668 times)

java

Re: May/June 2011 Request Thread

xxxxx

Re: May/June 2011 Request Thread

RoidRage

Re: May/June 2011 Request Thread

java

Re: May/June 2011 Request Thread

java

Re: May/June 2011 Request Thread

java

Re: May/June 2011 Request Thread

RoidRage

Re: May/June 2011 Request Thread

RoidRage

Re: May/June 2011 Request Thread

java

Re: May/June 2011 Request Thread

Enkidu

Re: July 2011 Request Thread

java

Re: July 2011 Request Thread

java

Re: July 2011 Request Thread

RoidRage

Re: July 2011 Request Thread

RoidRage

Re: July 2011 Request Thread

java

August 2011 Reference Request Thread

JustDreaming

Re: August 2011 Reference Request Thread

java

Re: August 2011 Reference Request Thread

reDEEMed

Re: August 2011 Reference Request Thread

java

Re: August 2011 Reference Request Thread

java

Re: August 2011 Reference Request Thread