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Tranglycosylation reactions with glycosyl azides as glycosyl donors.107

Trani-polyacetylene.

Trani-Ru.

Trannent absorption q ectra obtained on pulse radiotysis of N20-saturated obtained on pulse radk tysis of NjO-saturated neutral aqueous solution .

Tranperatiue dependraice of the Raman in-phase .

Tranrformation of BnHi if into upon addition of BH3

Trans 1 ratio from isomerization of ru-2-butene over metal sulfates on silica gel plotted against the electronegativity of metal ion.

Trans 1,4-polybutadiene

Trans activated complexes for typical secondary insertion

Trans and cis butene

Trans and cis configuration of a 042 octahedron

Trans and cis isomers of 4-alkyl substituted aniline.

Trans and Cis Peptide Bonds. The trans form is strongly favored because of steric clashes that occur in the cis form.

Trans and Cis X-Pro Bonds. The energies of these forms are relatively balanced because steric clashes occur in both forms.

Trans and cis X-Pro bonds. The energies of these forms are similar to one another because steric dashes occur in both forms.

Trans and cis- 1,3-cyclopropane

Trans and gauche conformers of the IV-butylimidazolium group as represented by a Newman projection.

Trans and gauche conformers of the jV-butylimidazolium group as represented by a Newman projection.

Trans and gauche isomers of PET.

Trans cis ratio of but-2-ene as a function of the amount of butenes for the four carbenes during the

Trans configuration in the pyrrolidine substituents giving rise to an additive effect in the CD peak at 425-430 nm. On the other hand, cis isomers present less pronounced peaks in that region, the effect of the heavier aromatic moiety being predominant with respect to the ester group.

Trans conformation of the single-bonded along the dimer axis .

Trans di-n-propylporphyrazine. Adapted from .

Trans ds-lAyniom vs. rra i cw-2-pentene in the metathesis of cw-2-pentene with

Trans effect by tethered coordinating functional groups .



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