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American Chemical Society Green

ACS GCI American Chemical Society Green Chemistry Institute... [Pg.418]

ACS CGI (2010) ACS GCI Pharmaceutical Roundtable 2010 Year in Review. American Chemical Society Green Chemistry Institute. Washington, DC, http //portal.acs.org/portal/ PublicWeb Site / greenchemistry/ industriainnovation / roundtable/ CNBP 026603 (last accessed October 23,... [Pg.449]

American Chemical Society. Green Chemistry Meeting Global Challenges, Green Chemistry on DVD, American Chemical Society Washington, 2002. [Pg.322]

American Chemical Society. Green Chemistry Educational Resources. http //portal.acs.org/portal/PublicWebSite/greenchemistry/education/resourc es/index.html (accessed Jun 6, 2008). [Pg.101]

Figure 15.6 Example output of the process mass intensity and life cycle assessment tool developed by the American Chemical Society Green Chemistry Institute Pharmaceutical Roundtable. The data presented in the columns provide the metrics for steps 1,2, 3, and the total of the synthesis. Some of the instructions in the tool are included as an illustration. Figure 15.6 Example output of the process mass intensity and life cycle assessment tool developed by the American Chemical Society Green Chemistry Institute Pharmaceutical Roundtable. The data presented in the columns provide the metrics for steps 1,2, 3, and the total of the synthesis. Some of the instructions in the tool are included as an illustration.
American Chemical Society, green chemistry resources, ACS homepage http // www.acs.org/ education/greenchem/. [Pg.311]

Green Chemistry (2013) The twelve Principles of Green Chemistry, American Chemical Society Green Chemistry Institute, http //www.acs.org/content/acs/en/ greenchemistry/about/principles/12-principles-of-green-chemis try.html. [Pg.12]

S. C. DeVito, ia S. C. DeVito and R. L. Garrett, eds.. Designing Safer Chemicals Green Chemistry for Pollution Prevention, American Chemical Society Symposium Series 640, American Chemical Society, Washington, D.C., pp. 194—223. [Pg.227]

Green DVS. Automated three-dimensional structure generation. In Martin YC and Willett P, editors, Designing bioactive molecules. Three-dimensional techniques and applications. Washington DC, American Chemical Society, 1998 47-71. [Pg.206]

G.R. Carlson in Green Chemical Syntheses and Processes , P.T. Anastas, L. G. Heine and T. C. Williamson, (eds), ACS Symposium Series 767, American Chemical Society, Washington D.C., 2000. [Pg.290]

Figure 16. Projections onto 2D surfaces of trajectories (in green) of CH3O H2 + HCO. The left column is a projection onto the surface of Fig. 15. The right column is a projection onto the surface of Fig. 14. The black contour represents the saddle point energy for the H+ H2CO H2 + HCO reaction. Blue contours are lower in energy red contours are higher. Reprinted with permission from [67], Copyright 2001 American Chemical Society. (See color insert.)... Figure 16. Projections onto 2D surfaces of trajectories (in green) of CH3O H2 + HCO. The left column is a projection onto the surface of Fig. 15. The right column is a projection onto the surface of Fig. 14. The black contour represents the saddle point energy for the H+ H2CO H2 + HCO reaction. Blue contours are lower in energy red contours are higher. Reprinted with permission from [67], Copyright 2001 American Chemical Society. (See color insert.)...
Denis, J.N., Greene, A.E., Guenard, D., Gueritte-Voegelein, F., Mangatal, L., Potier, P. (1988) A Highly Efficient, Practical Approach to Natural Taxol. Journal of the American Chemical Society, 110, 5917-5919. [Pg.195]

Gann, M.C. Connelly, M.E. (2000) Real World Cases in Green Chemistry. American Chemical Society, Washington, DC. http //www.chemistry.org/portal/resources/ACS/ACSContent/ education/greenchem/case.pdf. [Pg.247]

G.C. Mattem, C.I. Nuessle, D.L. Green, W.M. Leimkuehler, J.D. Philpot, RJ. Ness, and K.S. Billesbach, Accelerated field residue analysis of tebuconazole using Soxtec extraction and HPLC/electrospray tandem mass spectrometry (HPLC/ESI-MS-MS), Presented at the Midwest Regional Meeting of the American Chemical Society, Osage Beach, MO, October 29, 1997. [Pg.1241]

Weinstein, H., R. Osman, and J. P. Green. 1979. The Molecular Basis of Structure-Activity Relationships Quantum Chemical Recognition Mechanisms in Drug-Receptor Interactions. In Computer-Assisted Drug Design. E. C. Olson and R. E. Christofferson, eds. American Chemical Society, Washington, D.C. [Pg.83]

Figure 9.10 (a) Core of [Ln(lll)8Co(ll)8(OH)4(N03)4(03PtBu)8(02C,Bu)16] with connecting O-based ligands. Key Ln(lll) purple Co(ll) blue N turquoise P green O yellow, (b) Cartoon of the same. (Taken from Ref. [32] with permission American Chemical Society.)... [Pg.310]

Fig. 4 (a) Model for an in-register parallel (l-sheet for REDOR simulations. Only the backbone is shown and the residue labels correspond to the sequence of Af), 40. Relevant distances between Phe20 amide nitrogens (blue in color) and backbone carbonyl sites (dark green in color) are shown, (b) Model for an antiparallel [1-sheet with 17 + k <-> 21 — k registry. (Figure and caption adapted from [51]. Copyright 2009 American Chemical Society)... [Pg.59]

Figure 3.2 Ribbon diagram of the C-lobe of human transferrin with the two domains shown in different colours (cyan for Cl and green for C2). The inset shows the four protein ligand residues together with the arginine residue which stabilizes binding of the synergistic carbonate ion (both in magenta). (Reprinted with permission from Mason et al., 2005. Copyright (2005) American Chemical Society.)... Figure 3.2 Ribbon diagram of the C-lobe of human transferrin with the two domains shown in different colours (cyan for Cl and green for C2). The inset shows the four protein ligand residues together with the arginine residue which stabilizes binding of the synergistic carbonate ion (both in magenta). (Reprinted with permission from Mason et al., 2005. Copyright (2005) American Chemical Society.)...
Figure 13.24 Structures of sMMO components and proposed reaction cycle, (a) MMOH (b) the MMOR FAD and ferredoxin (Fd) domains (c) MMOB. In MMOH the ot, P and y subunits are coloured blue, green and purple, respectively. Iron, sulfur and FAD are coloured orange, yellow and red, respectively and are depicted as spheres. The MMO reaction cycle is shown on the right, with atoms coloured [Fe (black), C (grey), O (red) and N (blue)]. (Reprinted with permission from Sazinsky and Lippard, 2006. Copyright (2006) American Chemical Society.)... Figure 13.24 Structures of sMMO components and proposed reaction cycle, (a) MMOH (b) the MMOR FAD and ferredoxin (Fd) domains (c) MMOB. In MMOH the ot, P and y subunits are coloured blue, green and purple, respectively. Iron, sulfur and FAD are coloured orange, yellow and red, respectively and are depicted as spheres. The MMO reaction cycle is shown on the right, with atoms coloured [Fe (black), C (grey), O (red) and N (blue)]. (Reprinted with permission from Sazinsky and Lippard, 2006. Copyright (2006) American Chemical Society.)...
Figure 16.5 Resulting pharmacophore for P-gp actively transported molecules. The depicted molecule is the analgesic (narcotic) sufentanil. The colored areas around the molecules are the GRID fields produced by the molecule yellow for DRY probe, green for TIP probe and blue for N1 probe. Reprinted with permission from ref. [53], Copyright 2005 American Chemical Society. Figure 16.5 Resulting pharmacophore for P-gp actively transported molecules. The depicted molecule is the analgesic (narcotic) sufentanil. The colored areas around the molecules are the GRID fields produced by the molecule yellow for DRY probe, green for TIP probe and blue for N1 probe. Reprinted with permission from ref. [53], Copyright 2005 American Chemical Society.
A. Dequasie, The Green Flame, American Chemical Society, Washington, DC, 1991. [Pg.90]

Fig. 6 Typical PET probes (a) and representative fluorescence light-up responses toward selected metal ions in tabulated (b) and graphical form (c trace 1 = 14, trace 2 = 14-(Zn2+)2, trace DMA = 9,10-dimethylanthracene in MeCN). Color code coordinating atoms in blue, atoms which take part in the complexation and show (main, in 14) PET activity in orange, fluorophore in green. Lincoln and co-workers have demonstrated that the attachment of two dimethylamino groups through propylene spacers to the 9,10-positions of anthracene has a more than 100-fold weaker PET activity than the attachment through methylene spacers [62]. The blue N atoms in 14 are thus predominantly responsible for coordination. For symbols, see Fig. 3. Quantum yield of 14 in MeCN estimated from intensity readings published in [61] and quantum yield data of the parent compound without active PET, DMA, published in [63]. (Reprinted in part with permission from [61]. Copyright 1988 American Chemical Society)... Fig. 6 Typical PET probes (a) and representative fluorescence light-up responses toward selected metal ions in tabulated (b) and graphical form (c trace 1 = 14, trace 2 = 14-(Zn2+)2, trace DMA = 9,10-dimethylanthracene in MeCN). Color code coordinating atoms in blue, atoms which take part in the complexation and show (main, in 14) PET activity in orange, fluorophore in green. Lincoln and co-workers have demonstrated that the attachment of two dimethylamino groups through propylene spacers to the 9,10-positions of anthracene has a more than 100-fold weaker PET activity than the attachment through methylene spacers [62]. The blue N atoms in 14 are thus predominantly responsible for coordination. For symbols, see Fig. 3. Quantum yield of 14 in MeCN estimated from intensity readings published in [61] and quantum yield data of the parent compound without active PET, DMA, published in [63]. (Reprinted in part with permission from [61]. Copyright 1988 American Chemical Society)...
Fig. 9.18 (a) Schematic of the device, which was designed for simultaneous measurement of the SWNT network capacitance and conductance, (b) Dependence of the network capacitance (red) and conductance (green) on the substrate voltage, FS. The network capacitance is approximately 1/4 the value of the capacitance for a parallel-plate capacitor with an equivalent area and oxide thickness (Kong et al., 2003. With the permission from American Chemical Society) (See Color Plates)... [Pg.199]


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