Ѕиологический каталог




Ѕиоорганическа€ хими€

јвтор √.ƒюга,  .ѕенни

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102. Hein G. E., Niemann C. Steric course and specificity of a-chymotrypsin-cata-lyzed reactions. II. J. Amer. Chem. Soc. 84, 4495Ч4503 (1962).

103. Dugas H. The stereospecificity of subtilisin BPN' towards l-keto-3-car-bomethoxy-l,2,3,4-tetrahydroisoquinoline. Can. J. Biochem. 47, 985Ч987 (1969).

104. Silver M. S., Sone T. Stereospecificity in the hydrolysis of conformationally homogenous substrates by a-chymotrypsin. J. Amer. Chem. Soc. 90, 6193Ч 6198 (1968).

105. Cohen S. G., Schultz R. M. The active site of a-chymotrypsin. J. Mol. Biol. 243, 2607Ч2617 (1968).

106. Belleau ¬., Chevalier R. The absolute conformation of chymotrypsin-bound substrates. Specific recognition by the enzyme of biphenyl asymmetry in a constrained substrate. J. Amer. Chem. Soc. 90, 6864Ч6866 (1968).

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110. Pincus M. R., Scheraga H. A. Conformational energy calculation of enzyme-substrate and enzyme-inhibitor complexes of lysozyme. 2. Calculation of the structures of complexes with a flexible enzyme. Macromolecules 12, 633Ч644 (1979).

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115. Deslongchamps P. Stereoelectronic control in hydrolytic reactions. 26th IUPAC, Tokyo, Japan, 1977.

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118. Bizzozero S. A., Zweifel ¬. O. The importance of the conformation of the tetrahedral intermediate for the a-chymotrypsin-catalyzed hydrolysis of peptide substrates. FEBS Lett. 59, 105Ч108 (1975).

119. Petkov D., Christova E., Stoineva I. Catalysis and leaving group binding in anilide hydrolysis by chymotrypsin. Biochim. Biophys. Acta 527, 131Ч141 (1978).

120. Gorenstein D. G.. Flndlay J. ¬., Luxon B. A., Kar D. Stereoelectronic control in carbon-oxygen and phosphorus-oxygen bond breaking processes. Ab initio calculation and speculations on the mechanism of ribonuclease A, staphylococcal nuclease and lysozyme. J. Amer. Chem. Soc. 99. 3473Ч3479 (1977).

Ћитература

493

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125. Sucking C. J. Immobilized enzymes. Chem. Soc. Rev. 6, 215Ч233 (1977). 126 Pollak A., Baughn R. L., Adalsteinsson O., Whitesides G. M. Immobilization

of synthetically useful enzymes by condensation polymerization. J. Amer. Chem. Soc. 100, 302Ч304 (1978).

127. Guilbault G. G., Sadar M. H. Preparation and analytical uses of immobilized enzymes. Acc. Chem. Res. 12, 344Ч359 (1979).

128. Mosbach K, Larsson P. O. Preparation and application of polymer-entrapped enzymes and microorganisms in microbial transformation processes with special reference to steroid 1 l-|3-hydroxylation and ƒ'-dehydrogenation. Bio-technol. Bioeng. 13, 19Ч27 (1970).

129. Suf P. A., Kay S., Lilly M. D. The conversion of benzyl penicillin to 6-ami-nopenicillanic acid using an insoluble derivative of penicillin amidase. Bio-technol. Bioeng. 12, 337Ч348 (1969).

130. Fife “. H. Intramolecular nucleophilic attack on esters and amides. In: Bioorganic Chemistry (E. E .van Tamelen, Ed.), Vol. 1, Chap. 5, pp. 93Ч116. Academic Press, New York, 1977.

131. Bender M. L., Komiyama M. In: Bioorganic Chemistry (E. E. van Tamelen, Ed.), Vol. I, Chap 2, pp. 19Ч57. Academic Press, New York, 1977.

132. Pedersen —. I. Cyclic polyethers and their complexes witb metal salts. J. Amer. Chem. Soc. 89, 2495Ч2496 (1967).

133. Pedersen C. J., Cyclic polyethers and their complexes with metal salts. J. Amer. Chem. Soc. 89, 7017Ч7036 (1967).

134. Cram D. I., Cram I. M. Host-guest chemistry. Science 183, 803Ч809 (1974).

135. Cram D. /., Cram I. M. Design of complexes between synthetic hosts and organic guests. Acc. Chem. Res. 11, 8Ч14 (1978).

136. Cram D. I. Applications of Biochemical Systems in Organic Chemistry. In: Techniques of Chemistry Series (J. B. Jones, C. J. Sih, D. Perlman, Eds.), Vol. 10, Part II, Chap. 5, pp. 815Ч874. Wiley-Intersciense, New York, 1976.

137. Cram D. I. et al. Host-guest complexation. 1. Concept and illustration J. Amer. Chem. Soc. 99, 2564Ч2571 (1977).

138. Cram D. I. et al. Host-guest complexation. 3. Organization of pyridyl binding sites. J. Amer. Chem. Soc. 99, 6392Ч6398 (1977).

139. Warshawsky A., Kalir R., Deshe A., Berkovitz H., Patchornik A. Polymeric pseudocrown ethers. 1. Synthesis and complexation with transition metal anions. J. Amer. Chem. Soc. 101, 4249Ч4258 (1979).

140. Curtis W. D., Laidler D. A., Stoddard J. F. To enzyme analogues by lock and key chemistry with crown compounds. I. Enantiomeric differentation by configurationally chiral cryptands synthesized from L-tartaric acid and D-man-nitol. J. Chem. Soc. Perkin Trans. 1, 1756Ч1769 (1977).

141. Stoddard J. F. From carbohydrates to enzyme analogues. Chem. Soc. Rev. 18, 85Ч142 (1979).

142. Hanessian S. Approaches to the total synthesis of natural products using Ђchiral templates* derived from carbohydrates. Acc. Chem. Res. 12, 159Ч165 (1979).

143. Chao Y., Cram D. I. Catalysis and chiral recognition through designed complexation of transition states in transacylations of amino ester salts. J. Amer. Chem. Soc. 98, 1015Ч1017 (1976).

144 Pearson R. G. Hard and soft acids and bases, HSAB, Part I. J. Chem. Educ 48, 581Ч587 (1968).

494

Ћитература

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146. Sunamoto /., Kondo H., Okamoto H., Murakami Y. Catalysis of the deacyla-tion of p-nitrophenyl hexadecanoate by 1 l-amino[20]paracyclophane-10-ol in neutral and alkaline media. Tetrahedron Lett. 1329Ч1332 (1977).

147. Murakami Y., Aoyama Y., Kada M., Kikuchi J. I. Macrocyclic enzyme model system: Catalysis of ester degradation by a [20]paracyclophane bearing nucleophilic and metal-binding sites. Chem. Commun. 494Ч496 (1978).

148 Lehn I. M., Sirlin C. Molecular catalysis: Enhanced rate of thiolysis with high structural and chiral recognition in complexes of a reactive receptor molecule. Chem. Commun. 949Ч951 (1978).

149. Lehn J. M. Cryptates: The chemistry of macropolycyclic inclusion complexes. Acc. Chem. Res. 11, 49Ч57 (1978).

150. Kirch K-, Lehn I. M. Selective transport of alkali metal cations through a liquid membrane by macrobicyclic carriers. Angew. Chem., Int. Ed. Engl. 14, 555Ч556 (1975).

151. Vogtle F., Weber E. Multidentate acyclic neutral ligands and their comple-- xation. Angew. Chem., Int. Ed. Engl. 18, 753Ч776 (1979).

152. Deber —. M., Blout E. R. Amino acid-cyclic peptide complexes. J. Amer. Chem. Soc. 96, 7566Ч7368 (1974).

153. Menger F. M. On the structures of micelles. Acc. Chem. Res. 12, 111Ч117 (1979).

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155. Cordes E. H., Dunlap R. B. Kinetics of organic reactions in micellar systems. Acc. Chem. Res. 2, 329Ч337 (1969).

156. Fisher L. R., Oakenfull D. G. Micelles in aqueous solution. Chem. Soc. Rev. 6, 25Ч42 (1977).

157. Menger F. M. In: Bioorganic Chemistry (E. E. van Tamelen, Ed.), Vol. Ill, Chap. 7, pp. 137Ч152. Academic Press, New York, 1977.

158. Fendler J. H., Fendler E. I. Catalysis in micelles and macromolecular systems. Academic Press, New York, 1975.

159. Baumucker J., Calzadilla M., Centeno M., Lehrmann G., Urdanela M., Lind-quist P., Dunham D., Price M., Sears ¬., Cordes E. H. Secondary valence force catalysis. XII. Enhanced reactivity and affinity of cyanide ion toward N-substituted 3-carbamoylpyridinium ions elicted by ionic surfactants and biological lipids. J. Amer. Chem. Soc. 94, 8164Ч8172 (1972).

160. Menger F. M., Donohue J. A., Williams R. F. Catalysis in water pools. J. Amer. Chem. Soc. 95, 286Ч288 (1973).

161. Escabi-Pirez J. R., Fendler J. H. Ultrafast excited state proton transfer in reversed micelles. J. Amer. Chem. Soc. 100, 2234Ч2236 (1978).

162. Shorenstein R. G., Pratt L. S., Hsu C. L, Wagner “. E. A model system for the study of equilibrium hydrophobic bond formation. J. Amer. Chem. Soc. 90, 6199Ч6207 (1968).

163. Moss R. A., Mahas R. G., Lukas T. L. A cystei

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