By Steven D. Burke, Rick L. Danheiser
Recognising the severe desire for bringing a convenient reference paintings that offers with the most well-liked reagents in synthesis to the laboratory of practicing natural chemists, the Editors of the acclaimed Encyclopedia of Reagents for natural Synthesis (EROS) have chosen crucial and necessary reagents hired in modern natural synthesis.
guide of Reagents for natural Synthesis: Oxidizing and lowering brokers, presents the artificial chemist with a handy compendium of knowledge targeting an important and often hired reagents for the oxidation and relief of natural compounds, extracted and up-to-date from EROS. The inclusion of a bibliography of stories and monographs, a compilation of natural Syntheses techniques with verified experimental information and references to oxidizing and decreasing brokers will make sure that this guide is either finished and handy.
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Additional info for Handbook of reagents for organic synthesis
JACS 1984,106, 1845. (e) Bumell, D. ; Valenta, Z. CC 1985, 1247. ; Zope, U. ; Ayyangar, N. R. SC 1989,19,585. ; Craig, T. A. T1981,37, 4081. ; Reddy, D. ;Murty, A. N. CC 1983,824. Krohn, K. TL 1980,21,3557. Gupta, R. ; Raynor, C. ; Stoodley,R. ; Slawin, A. M. ; Williams, D. J. JCS(P1J 1988, 1773. McDougal, P. ; Jump, J. ; Rico, J. G. TL 1989,30, 3897. Dauben, W. ; Bunce, R. A. TL 1982,23,4875. Monti, S. A. JOC 1966,31,2669. Kushch, S. ; Izakovich, E. ; Khidekel, M. ; Strelets, V. V. IZV 1981, 7,1500 (CA 1981,95, 149 595s).
Nicolaou, K. ; Dolle, R. ; Randal, J. L. CC 1984, 1153. ; Marhenke, R. ; Eustace, E. J. JOC 1973, 38, 1428. (b) Smith, M. ; Wolinsky, J. JOC 1981,46, 101. ; Yarnarnoto, H. SL 1991, 255. Lansbury, P. ; Scharf, D. A. JOC 1967, 32, 1748. Elsenbaumer, R. ; Mosher, H. ; Momson, J. ; Tornaszewski, J. E. JOC 1981,46,4034. Corey, E. ; Katzenellenbogen,J. ; Posner, G. H. JACS 1967,89,4245. ; Sato, M. JOM 1977, 142, 71. 4. JACS 1979,101, 7302. ; Krantz, A. JACS 1987,109,3491. Paul Galatsis University of Guelph, Ontario, Canada Dialkylaluminum hydrides also behave as hydroalumination reagents (see Diisobutykduminum Hydride) and are more commonly used than AlH3.
G. TL 1989,30, 3897. Dauben, W. ; Bunce, R. A. TL 1982,23,4875. Monti, S. A. JOC 1966,31,2669. Kushch, S. ; Izakovich, E. ; Khidekel, M. ; Strelets, V. V. IZV 1981, 7,1500 (CA 1981,95, 149 595s). 47) [136705-64-11 (ligand for asymmetric catalysis;' rhodium complexes are efficient catalyst precursors for highly enantioselective hydrogenation of a-(N-acylarnino)acrylates,'*' enol acetates,' and N-acylhydra~ones~,~) Alternate Name: (R,R)- and (S,S)-Ethyl-DuPHOS. 045 mmHg; (R,R)-EthylDuPHOS, [a]i5= -265" (c 1, hexane).