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Initiator-terminator gap

Scheme 8-22 Bis-lactonization experiments to measure the effective initiator-terminator gap in the (NBD)3-derived template. Scheme 8-22 Bis-lactonization experiments to measure the effective initiator-terminator gap in the (NBD)3-derived template.
Similar functionalization chemistry with the (NBD)4-derived diester 50 afforded the trichloroacetyl, phenylthiomethacrylate-bearing template 67 whose initiator-terminator pair spans an approximately 17 A gap (Scheme 8-20). Single-crystal X-ray analysis of the phenylthio-containing species 63 provided a detailed glimpse of the fully functionalized template (63, Scheme 8-20). The anthracene-derived endcaps appear bowed slightly away from the apical exo hydrogens of the proximal norbomane units, as predicted by the molecular mechanics-based structural model 63". These distortions are unlikely to have any consequence for the planned chemistry. [Pg.233]

Figure 13.12 motor end-plate. The axon terminates very close to the muscle. They are separated by a small gap (the synaptic cleft). When the nerve is stimulated, acetylcholine is released into the cleft where it diffuses across the cleft, and then binds to receptors located on the muscle side of the cleft and initiates an action potential along the sarcolemma. [Pg.284]

The excimer fluorescence (with respect to the excited vdW dimer emission) is red shifted and structureless because the emission is terminated in a repulsive ground-state potential energy surface (Figure 15). For parallel transition moments, emission from the out-of-phase exciton state to the ground state is forbidden and for the in-phase exciton state emission is allowed [28a]. It should be noted, however, that the forbidden emission from the out-of-phase exciton state is expected to have a similar transition dipole moment as the Lb So emission. The actual dynamics of the initially excited vdW dimer depend on the energy gap and the coupling strength between the primary excited (LE) state and the excimer state. [Pg.3095]

A list of key differences between prokaryotes and eukaryotes with respect to protein synthesis is shown in Table 9-1. These include the existence of multiple eukaryotic initiation factors that facilitate the assembly of the riboso-mal protein synthetic machinery, whereas there are only three for prokaryotes. An initiation site on bacterial mRNA consists of the AUG initiation codon preceded with a gap of approximately 10 bases by the Shine-Dalgamo polypurine hexamer, whereas the 5 Cap (a 7-methylguanylate residue in a 5 —>5 triphosphate linkage) acts as an initiation signal in eukaryotes. In prokaryotes, the first or A-terminal amino acid is a formyl-methionine (fMet), but in eukaryotes it is usually a simple methionine. Additionally, the size and nature of the prokaryotic ribosomes are quite different from the eukaryotic ribosomes. [Pg.87]


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See also in sourсe #XX -- [ Pg.235 , Pg.238 ]




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