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Reboud-Ravaux, Michele (1980) N-Acetylbenzotriazole hydrolysis and aminolysis. Broensted relationships and rate-determining steps in the uncatalyzed and catalyzed aminolysis. Journal Of The American Chemical Society, 102 (3) 1039-1046 doi:10.1021/ja00523a022

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Reference TypeJournal (article/letter/editorial)
TitleN-Acetylbenzotriazole hydrolysis and aminolysis. Broensted relationships and rate-determining steps in the uncatalyzed and catalyzed aminolysis
JournalJournal Of The American Chemical Society
AuthorsReboud-Ravaux, MicheleAuthor
Year1980 (January)Volume102
Issue3
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00523a022Search in ResearchGate
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Mindat Ref. ID1366125Long-form Identifiermindat:1:5:1366125:8
GUID0
Full ReferenceReboud-Ravaux, Michele (1980) N-Acetylbenzotriazole hydrolysis and aminolysis. Broensted relationships and rate-determining steps in the uncatalyzed and catalyzed aminolysis. Journal Of The American Chemical Society, 102 (3) 1039-1046 doi:10.1021/ja00523a022
Plain TextReboud-Ravaux, Michele (1980) N-Acetylbenzotriazole hydrolysis and aminolysis. Broensted relationships and rate-determining steps in the uncatalyzed and catalyzed aminolysis. Journal Of The American Chemical Society, 102 (3) 1039-1046 doi:10.1021/ja00523a022
In(1980, January) Journal Of The American Chemical Society Vol. 102 (3) American Chemical Society (ACS)

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REBOUD-RAVAUX, M. (1980) ChemInform Abstract: N-ACETYLBENZOTRIAZOLE HYDROLYSIS AND AMINOLYSIS. BROENSTED RELATIONSHIPS AND RATE-DETERMINING STEPS IN THE UNCATALYZED AND CATALYZED AMINOLYSIS. Chemischer Informationsdienst, 11 (19) doi:10.1002/chin.198019086
Gresser, M. J., Jencks, W. P. (1977) Ester aminolysis. Structure-reactivity relationships and the rate-determining step in the aminolysis of substituted diphenyl carbonates. Journal Of The American Chemical Society, 99 (21) 6963-6970 doi:10.1021/ja00463a032
Maugh, Tom II, Bruice, Thomas C. (1971) Hydrolysis and aminolysis of O-acylhydroxyquinolines. Intracomplex general base-catalyzed aminolysis. Journal Of The American Chemical Society, 93 (24) 6584-6591 doi:10.1021/ja00753a043
GRESSER, M. J., JENCKS, W. P. (1978) ChemInform Abstract: ESTER AMINOLYSIS. STRUCTURE-REACTIVITY RELATIONSHIPS AND THE RATE-DETERMINING STEP IN THE AMINOLYSIS OF SUBSTITUTED DIPHENYL CARBONATES. Chemischer Informationsdienst, 9 (3) doi:10.1002/chin.197803184
Fife, Thomas H., DeMark, B. R. (1979) General-base-catalyzed intramolecular aminolysis of thiol esters. Cyclization of S-n-propyl o-(2-imidazolyl)thiolbenzoate. Relationship of the uncatalyzed and base-catalyzed nucleophilic reactions. Journal Of The American Chemical Society, 101 (24) 7379-7385 doi:10.1021/ja00518a041
Felton, Stephen M., Bruice, Thomas C. (1969) Intramolecular general-base-catalyzed hydrolysis and aminolysis of the ester bond by imidazole and quinoline bases. Journal Of The American Chemical Society, 91 (24) 6721-6732 doi:10.1021/ja01052a031
Hogan, John Charles, Gandour, Richard David (1980) The remarkable catalytic power of glymes in ester aminolysis carried out in nonpolar media. Journal Of The American Chemical Society, 102 (8) 2865-2866 doi:10.1021/ja00528a071
FIFE, T. H., DEMARK, B. R. (1980) ChemInform Abstract: GENERAL-BASE-CATALYZED INTRAMOLECULAR AMINOLYSIS OF THIOL ESTERS. CYCLIZATION OF S-N-PROPYL O-(2-IMIDAZOLYL)THIOLBENZOATE. RELATIONSHIP OF THE UNCATALYZED AND BASE-CATALYZED NUCLEOPHILIC REACTIONS. Chemischer Informationsdienst, 11 (9) doi:10.1002/chin.198009103
Page, Michael I., Jencks, William P. (1972) Uncatalyzed aminolysis of acetylimidazole. Limiting product-like transition state for acyl transfer. Journal Of The American Chemical Society, 94 (9) 3263-3264 doi:10.1021/ja00764a077
Hawkins, Peter J., Piscalnikow, Ivan (1955) A Kinetic Study of the Aminolysis and Hydrolysis of α-Naphthyl Acetate. Journal Of The American Chemical Society, 77 (10) 2771-2773 doi:10.1021/ja01615a030
Koehler, K., Sandstrom, W., Cordes, E. H. (1964) Concerning the Mechanism of the Hydrolysis and Aminolysis of Schiff Bases. Journal Of The American Chemical Society, 86 (12) 2413-2419 doi:10.1021/ja01066a024
 
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