New directions in aromatic nucleophilic substitution

作者: John A. Zoltewicz

DOI: 10.1007/BFB0046186

关键词:

摘要: … diethyl phosphate reactants is especially significant because they are readily prepared from anilines and phenols, respectively. This method of substitution is preferred over an aryne …

参考文章(118)
John A. Zoltewicz, Larry S. Helmick, Terry M. Oestreich, Roy W. King, Paul E. Kandetzki, Addition of amide ion to isoquinoline and quinoline in liquid ammonia. Nuclear magnetic resonance spectra of anionic .sigma. complexes Journal of Organic Chemistry. ,vol. 38, pp. 1947- 1949 ,(1973) , 10.1021/JO00950A036
Reinhard W. Hoffmann, Dehydrobenzene and Cycloalkynes ,(2012)
Heinz Günter Viehe, Chemistry of Acetylenes ,(1969)
Ellis K. Fields, Seymour Meyerson, Mechanisms of Formation and Reactions of arynes at high Temperatures Advances in Physical Organic Chemistry. ,vol. 6, pp. 1- 61 ,(1968) , 10.1016/S0065-3160(08)60253-1
F. Sanger, The terminal peptides of insulin Biochemical Journal. ,vol. 45, pp. 563- 574 ,(1949) , 10.1042/BJ0450563
Calvin D. Ritchie, Nucleophilic reactivities toward cations Accounts of Chemical Research. ,vol. 5, pp. 348- 354 ,(1972) , 10.1021/AR50058A005
Jerry Kramer, R. Stephen Berry, Gaseous 3,4-pyridyne and the formation of diazabiphenylene Journal of the American Chemical Society. ,vol. 94, pp. 8336- 8347 ,(1972) , 10.1021/JA00779A010