Stereoelectronic Properties of Tetrahedral Species Derived from Carbonyl Groups. Ab initio study of aminodihydroxymethane, CH(OH)2NH2, a model tetrahedral intermediate in amide hydrolysis
暂无分享,去创建一个
[1] Jack D. Dunitz,et al. Stereochemistry of reaction paths at carbonyl centres , 1974 .
[2] Ab initio study of the amidic bond cleavage by hydroxide(1-) ion in formamide , 1975 .
[3] S. Huzinaga,et al. Gaussian‐Type Functions for Polyatomic Systems. II , 1970 .
[4] D. Gorenstein,et al. Conformational study of cyclic and acyclic phosphate esters. CNDO/2 calculations of angle strain and torsional strain. , 1976, Journal of the American Chemical Society.
[5] N. D. Epiotis,et al. Directional effects of .sigma. conjugation on geometrical isomerism , 1977 .
[6] Leo Radom,et al. The application of ab initio molecular orbital theory to the anomeric effect. A comparison of theoretical predictions and experimental data on conformations and bond lengths in some pyranoses and methyl pyranosides , 1972 .
[7] C. Moreau,et al. The Importance of Conformation in the Ozonolysis of Acetalsl , 1972 .
[9] J. Lehn,et al. Stereoelectronic Properties, Stereospecificity and Stabilization of α‐Seleno Carbanions. An ab initio Study , 1977 .
[10] D. Gorenstein,et al. Effect of bond angle distortion on torsional potentials. Ab initio and CNDO/2 calculations on dimethoxymethane and dimethyl phosphate , 1977 .
[11] L. Salem,et al. Superjacent orbital control. Interpretation of the anomeric effect , 1973 .
[12] P. Deslongchamps. The importance of conformation of the tetrahedral intermediate in the hydrolysis of esters and amides , 1975 .
[13] P. Siegbahn,et al. Gaussian basis sets for the first and second row atoms , 1970 .
[14] Saul Wolfe,et al. Gauche effect. Stereochemical consequences of adjacent electron pairs and polar bonds , 1972 .
[15] S. F. Boys,et al. Canonical Configurational Interaction Procedure , 1960 .
[16] D. W. Mayo,et al. Infrared frequency effects of lone pair interactions with antibonding orbitals on adjacent atoms , 1976 .
[17] P. Deslongchamps. Stereoelectronic control in the cleavage of tetrahedral intermediates in the hydrolysis of esters and amides , 1975 .
[18] C. Grob. Mechanismen und Stereochemie der heterolytischen Fragmentierung , 1969 .
[19] I. Csizmadia,et al. An ab initio study of the AAc1 hydrolysis mechanism of formamide , 1973 .
[20] J. Lehn,et al. Stereoelectronic effects. 5. Stereoelectronic properties, stereospecificity, and stabilization of .alpha.-oxa and .alpha.-thia carbanions , 1976 .
[21] Frank E. Harris,et al. Molecular Orbital Theory , 1967 .
[22] S. Benkovic,et al. Studies on models for tetrahydrofolic acid. 8. Hydrolysis and methoxyaminolysis of amidines , 1977 .
[23] L. Salem,et al. Lone pairs in organic molecules: Energetic and orientational non-equivalence : Stereochemical consequences , 1974 .
[24] J. Dunitz,et al. Chemical reaction paths. IV. Aspects of O⋯C = O interactions in crystals , 1974 .
[25] J. Lehn,et al. Stereoelectronic properties and reactivity of the tetrahedral intermediate in amide hydrolysis. Nonempirical study of aminodihydroxymethane and relation to enzyme catalysis. , 1974, Journal of the American Chemical Society.
[26] S. Bizzozero,et al. The importance of the conformation of the tetrahedral intermediate for the α‐chymotrypsin‐catalyzed hydrolysis of peptide substrates , 1975, FEBS letters.
[27] Leo Radom,et al. Molecular orbital theory of the electronic structure of organic compounds. XVIII. Conformations and stabilities of trisubstituted methanes , 1973 .
[28] S. C. Nyburg,et al. X-ray analysis of the structure and correlation with the spectra of haplophytine , 1976 .
[29] H. Schlegel,et al. Irrelevance of d-orbital conjugation. I. .alpha.-Thiocarbanion. Comparative quantum chemical study of the static and dynamic properties and proton affinities of carbanions adjacent to oxygen and to sulfur , 1975 .