Turner’s structures

Even though the use of Turner s structures to represent packed beds may be too complex, the overall concept of utilizing frequency-response experiments to construct detailed models is very interesting and might And use for other situations. 

Aris, R. 1959c. Diffusion and reaction in flow systems of Turner s structures. Chem Eng. Sci. 10 80-87. Aris, R., and R. Amundson. 1957. Some remarks on longitudinal mixing or diffusion in fixed beds. AIChE J. 3 280-282. 

Turner, S. Richard, 1 Two-component (2-K), nonsagging, polyurea structural adhesive, preparation of, 255-256 Two-component (2-K) systems, 238-241 Two-component (2-K) waterborne polyurethane coatings, 206 preparation of, 254-255 Two-shot cast elastomer, preparation of, 249-250... 

A comparison of the data obtained by using McDougal and Turner s treatment of the prediction of structured flow formation in the PVP-dextran system with the ternary diffusion data in Fig. 16 indicates that their theory is not compatible with our observations 36). 

Turner, S. Buseck, P. R. (1979) Manganese oxide tunnel structures and their intergrowths. Science, 203, 456-8. 

Romero, D.L., Tommasi, R.A., Janakiraman, M.N., Strohbach, J.W., Turner, S.R., et al. (1996) Structure-based design of HIV protease inhibitors 5,6-dihydro-4-hydroxy-2-pyrones as effective, nonpeptidic inhibitors. J. Med. Chem. 39 4630-4642. 

Turner S W P, Cabodi M, Craighead H G (2002). Confinement-induced entropic recoil of single DNA molecules in nanofluidic structure. Phys. Rev. Let. 88(12) 128103. Cabodi M, Turner S W P, Craighead H G (2002). Entropic recoil separation of long DNA molecules. Anal. Chem. 74 5169-5174. 

First, draw the structure of the compoimd in Crossfire s structure editor and search it against the Beilstein database. This brings up the record for the compound in question. A method of preparation using furfural and l-(3-nitrophenyl)ethanone is indicated under Reactions. If you follow the link to the Crossfire reaction record, you find two literature references D. L. Turner, /. Am. Chem. Soc. 71,1949, 612, and Li, Synth. Comm. 29,1999, 965. These articles describe methods of preparation from 2-furaldehyde and acetophenone. 

A., Apperley, D.C., McCann, M.C., Turner, S.R., and Jarvis, M.C. (2002) Structure of cellulose-deficient secondary cell walls from the irx3 mutant of Arabidopsis thaliana. Phytochemistry, 61 (1), 7-14. 

Turner MA et al Human argininosuccinate lyase a structural basis for intragenic complementation. Proc Natl Acad Sci U S A 1997 94 9063. 

Turner, J.V., Glass, B.D., and Agatanovic-kustrin, S. Prediction of dmg bioavailability based on molecular structure. Anal. Chim. Acta 2003, 485, 90-102. 

Turner, M. A., et al. (1998). Structure determination of selenomethionyl S-adenosyUiomocysteine hydrolase using data at a single wavelength. Nat. Struct. Biol. 5, 369-376. 

Ottersen, T., A. Aasen, F. S. El-Feraly and C. E. Turner. X-ray structure of cannabispiran A novel cannabis constituent. Chem Commun 1976 1976 580. 

Lai, S. D. and B. K. Yadav. Folk medicine of Kurushetra District (Haryana), India. EconBot 1983 37(3) 299-305. Me Phail, A. T., H. N. El Sohly, G. E. Turner and M. A. El Sohly. Stereochemical assignments for the two enantiomeric pairs of 9,10-dihydroxy-delta-6-alpha(10-alpha)-tetrahydro-cannabinols. X-ray crystal structure analysis of (DL)-trans-cannabitriol. Abstr 24th Annual Meeting American society of Pharmacognosy Univ Mississippi Oxford July 24-28 1983 ABSTR-50. 

Turner J.V., D.J. Maddalena, and S. Agatonovic-Kustrin (2004). BioavailabiUty prediction based on molecular structure for a diverse series of drugs. Pharmaceutical Research 21 68-82. 

A link between bacteria and tumor therapy was found early, at the beginning of the XVIII century [10]. By the end of the XIX century, Coley [11] developed a treatment for cancer with a mixture of bacterial toxins. In 1943 Shear and Turner [4] found that the antitumor effect of Coley s toxin was due to endotoxins, and after several decades it was shown that the biological activity of LPS was due to the lipid A [5]. We investigated the structures of lipids A with regard to their antitumor activities [12], finding that the optimum in vivo activity is obtained with diglucosamines acylated by 3 long chain fatty acids. 

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