N PERSPECTIVE

Fig. 5.n Perspective of the unit cell of the cubic 6-14 mixed halide phases, emphasizing the connectivity between the clusters (with the inner halides being omitted for clarity). 

Hadaway L, Chamallas SN. Vancomycin N perspectives on an old drug. J Infus Nuts 2003 26 278-284. 

Warner, I.M., El-Zahab, B., Siraj, N. Perspectives on moving ionic liquid chemistry into the solid phase. Anal. Chem. 86, 7184—7191 (2014)... 

Sahoo, G. C., Dutta, N. N. Perspectives in Liquid Membrane Extraction of Cephalosporin Antibiotics Vol. 75, p. 209... 

From a purely phenonienological perspective, this relationship describes a constant rate of change in the nonlhiear susceptibility of the surface with increasing adsorbate surface density N. Within a picture of... 

Fig. 10.27 Schematic representation of the energy landscape for protein folding. (Figure adapted from Onuchic ] N, Z Luthcy-Schulten and P Wolynes 1997. Theory of Protein Folding The Energy Landscape Perspective. Annual Reviews in Physical Chemistry 48 545-600.)...

J. I. Steiafeld, J. S. Francisco, and W. L. Hase, Chemical Kinetics and Dynamics, Prentice Hall, Englewood Chffs, N.J., 1989. Oriented more toward gas-phase reactions and iacludes more advanced microscopic iaterpretations from the perspective called chemical physics. 

A. B. Valansangkar and N. V. Ambre, Ocean Technology Perspectives, PubHcations and Information Directorate, New Delhi, India, pp. 827—841. 

Polyolefins—-A Global Perspective in a Decade ofi Change, Vol. 3, Technology and Economics, Chemical Systems, Tarrytown, N.Y., June 1991. 

The equihbtium lever relation, np = can be regarded from a chemical kinetics perspective as the result of a balance between the generation and recombination of electrons and holes (21). In extrinsic semiconductors recombination is assisted by chemical defects, such as transition metals, which introduce new energy levels in the energy gap. The recombination rate in extrinsic semiconductors is limited by the lifetime of minority carriers which, according to the equihbtium lever relation, have much lower concentrations than majority carriers. Thus, for a -type semiconductor where electrons are the minority carrier, the recombination rate is /S n/z. An = n — is the increase of the electron concentration over its value in thermal equihbtium, and... 

W. H. Lederer and R. J. Pensterheim, eds.. Arsenic Industrial, Biomedical, Environmental Perspectives, Van Nostrand Reinhold Co., Inc., N.Y., 1983. R. Reddy, ed. Arsenic Metallurgy-Fundamental and Applications, The Metallurgical Society (AIME), Warrendale, Pa., 1988. 

Pavletich, N.P., Pabo, C.O. Crystal structure of a five-finger GLI-DNA complex new perspectives on zinc fingers. Science 261 1701-1707, 1993. 

Perez, P., Pulgar, R., Olca-.Serrano, F., Villabos, M., Rivas, A., Metzler, M., Pedraza, V., and Olea, N. (1998). The estrogeniciry of bisphenol A-related diphenylalkanes with various sub.stit-uents at the central carbon and the hydroxy groups. Environ. Health Perspect. 106 3), 167-174. 

Pace, N. R., 1996. New perspective on the natural microbial world Molecular microbial ecology. ASM News 62 463-470. 

Murakami, Y. Functionaiited Cyclophanes as Catalysts and Enzyme Models. 115, 103-151 (1983). Mutter, M., and Pillai, V. N. R. New Perspectives in Polymer-Supported Peptide Synthesis. 106, 119-175 (1982). 

Probably the most widely applicable asymmetric imine aziridination reaction reported to date is that of Wulff et al. These workers approached the reaction from a different perspective, utilizing the so-called vaulted , axially chiral boron Lewis acids VANOL and VAPOL [35] to mediate reactions between ethyl diazoacetate and N-benzhydrylimines (Scheme 4.29) [36]. The reactions proceed with impressive enantiocontrol, but there is a requirement that the benzhydryl substituent be present since this group is not an aziridine activator there is, therefore, a need for deprotection and attachment of a suitable activating group. Nonetheless, this method is a powerful one, with great potential for synthesis, as shown by the rapid synthesis of chloroamphenicol by the methodology [37]. 

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