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C stereochemistry

Vladimir Prelog and John W. Comforth (V. P.) stereochemistry of organic molecules and reactions, (J. C.) stereochemistry of enzyme-catalyzed reactions... [Pg.6]

Flood, Thomas C., Stereochemistry of Reactions of Transition Metal-Carbon Sigma Bonds, 12, 37. Floss, Heinz G., Stereochemistry of Biological Reactions at Proprochiral Centers, 15, 253. Freedman, T. B., Stereochemical Aspects of Vibrational Optical Activity, 17, 113. [Pg.596]

If the product A- C- C- B occurs as the minor product, this presents a mismatched pair reaction, and the reagent with the opposite chirality should be used. The diastereofacial selectivity of the reagent must be large enough to outweigh that of A-C(x) in order to create the desired C- C stereochemistry with high selectivity. [Pg.54]

Zambelli, A. and Tosi, C. Stereochemistry of Propylene Polymerization. Vol. 15, pp. 31-60. Zucchini, U. and Cecchin, G. Control of Molecular-Weight Distribution in Polyolefins Synthesized with Ziegler-Natta Catalytic Systems. Vol. 51, pp. 101-154. [Pg.162]

C. Stereochemistry and Dynamic Behavior of [(rts1-C5HtC H4)Mo(CO)2(i]2-diene) Complexes... [Pg.339]

Flood, Thomas C., Stereochemistry of Reactions of Transition Metal-Carbon Sigma Bonds, 12,... [Pg.358]


See other pages where C stereochemistry is mentioned: [Pg.75]    [Pg.95]    [Pg.1287]    [Pg.163]    [Pg.187]    [Pg.252]    [Pg.218]    [Pg.157]    [Pg.248]    [Pg.97]    [Pg.244]    [Pg.176]    [Pg.117]    [Pg.132]    [Pg.186]    [Pg.51]    [Pg.164]    [Pg.151]    [Pg.178]    [Pg.167]    [Pg.225]    [Pg.323]    [Pg.339]    [Pg.104]    [Pg.167]    [Pg.187]    [Pg.194]    [Pg.168]    [Pg.104]    [Pg.167]    [Pg.263]    [Pg.292]    [Pg.300]    [Pg.161]    [Pg.161]    [Pg.128]    [Pg.214]    [Pg.302]    [Pg.130]    [Pg.204]    [Pg.74]    [Pg.232]   
See also in sourсe #XX -- [ Pg.104 ]




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