Download PDF by Hans J. Reich, James H. Rigby: Acidic and Basic Reagents , Handbook of Reagents for Organic

By Hans J. Reich, James H. Rigby

Recognising the serious desire for bringing a convenient reference paintings that bargains not just with the preferred reagents in synthesis to the laboratory of training natural chemists, the editors of the acclaimed 'Encyclopedia of Reagents for natural Synthesis' (EROS) have chosen an important and precious reagents hired in modern natural synthesis.

This e-book provides articles at the so much basic and flexible reagents for effecting natural changes that have been initially incorporated in EROS. In making a choice on candidate entries for inclusion during this specific assortment, the editors followed a extensive set of standards for outlining what precisely constitutes an acidic or uncomplicated reagent.

Each article includes the entire details present in EROS in addition to multiplied similar reagents listings. extra new listings of lately released assessment articles and monographs are integrated, in addition to proper 'Organic Syntheses' approaches that take care of both the arrangements or reactions of the featured reagents. This thorough and complete guide can have frequent allure.

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Anal. Chim. Ada. 1984, 759, 149. ; Commeyras, A. NJC 1983, 7, 83. 3. Yakobson, G. ; Furin, G. G. S 1980, 345. 4. (a) Olah, G. ; Nishimura, J. JACS 1974, 96, 2214. (b) Booth, B. ; Haszeldine, R. ; Laali, K. JCS(P1) 1980, 2887. 5. (a) Pozdnyakovich, Y. ; Shteingarts, V. D. JFC 1974, 4, 317. (b) Brovko, V. ; Sokolenko, V. ; Yakobson, G. G. JOU 1974, 10, 300. 6. Furin, G. ; Yakobson, G. ; Izv. Sib. Otd. Akad. Khim. ) 7. (a) Shteingarts, V. D. In Synthetic Fluorine Chemistry, Olah, G. ; Chambers, R.

V. BSB 1986, 95, 107. 3. Durham, L. ; McLeod, D. ; Cason, J. OSC 1963, 4, 635. 4. Miller, R. ; Nash, R. D. T 1974, 30, 2961. 5. ; Schuda, P. F. JACS 1979,101, 7020. 6. ; Urbach, H. TL 1983, 24, 5339. 7. Conant, J. ; Tuttle, N. OSC 1944, 1, 199. 8. Sinisten-a, J. ; Cabello, J. ; Marinas, J. M. S 1984, 502. 9. Alcantara, A. ; Marinas, J. ; Sinisterra, J. V. TL 1987, 28, 1515. 10. ; Sinisterra, J. V. S 1982, 1037. ; Marinas, J. ; Sinisterra, J. V. T 1987, 43, 2335. 11. 12. Sinisterra, J. ; Marinas, J.

38 (32) (24) AlCl 3 can also be used to catalyze [2 + 2] cycloaddition reac­ tions (eq 33) 43 and ene reactions (eq 34). 44 S:R = 82:18 (25) (33) (26) (34) (27) (28) Rearrangements. A1C13 catalyzed rearrangement of hydro­ carbon derivatives to adamantanes has been well documented (eq 35). 45 Other rearrangements have been used in triquinane syn­ thesis (eq 36). 46 (35) (29) Diels-Alder Reactions. There is some evidence that AlCl 3 catalysis of Diels-Alder reactions changes the transition state from a synchronous to an asynchronous one.

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