1.8: References
- Page ID
- 285620
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- For a recent monograph, see: "New Synthetic Routes to Prostaglandins and Thromboxanes", Roberts, S.M.; Scheinmann, F., Academic Press, New York (1982).
- Woodward, R.B.; Gosteli, J.; Ernest, I.; Friary, R.J.; Nestler, G.; Raman, H.; Sitrin, R.; Suter, C.; Whitesell, J.K. J. Am. Chem. Soc. 1973, 95, 6853.
- Brown, E.D.; Lilley, T.J. Chem. Commun. 1975, 39.
- Brewster, D.; Myers, M.; Ormerod, J.; Other, P.; Smith, A.C.B.; Spinner, M.E.; Turner, S. J. Chem. Soc. Perkin I, 1973, 2796.
- Corey, E.J.; Ohno, M.; Vatakencherry, P.A.; Mitra, R.B. J. Am. Chem. Soc. 1964, 86, 478.
- Volkmann, R.A.; Andrews, G.C.; Johnson, W.S. J. Am. Chem. Soc. 1973, 97, 4777.
- For an introduction to retrosynthetic analysis on a simple level see: Warren, S. "Organic Synthesis: The Disconnection Approach", Wiley-Interscence, New York (1982).
- For reviews see: (a) Wipke, W. T.; Howe, W. J. (Eds.) "Computer-Assisted Organic Synthesis", ACS Symposium Series volume 61, American Chemical Society, Washington, D. C. (1977); (b) Corey, E. J.; Long, A. K.; Rubenstein, S. D. Science 1985 228, 408.
- Hendrickson defined functionality level differently, i. e., as f = π + z where π = number of C-C π- bonds (identical with u = unsaturation level as defined on page 12) and z = number of carbon- heteroatom attachments: Hendrickson, J. B. Topics Current Chem. 1976, 62, 49. This definition has the desirable feature of indicating an equivalence for tautomers, e. g. Hendrickon's f = 2 for both ketones and their enols. As with our definition, Hendrickson's concept also recognizes that organic chemists view all carbinols, whether 1°, 2°, or 3° as functionally equivalent (f = 1), and that "there exist functional families which are easily interconverted for synthetic purposes": Hendrickson, J. B. J. Am. Chem. Soc. 1971, 93, 6847. But Hendrickson's f does not incorporate the concept of negative functionality levels engendered by metals or other elements, e. g. silicon, that may serve as electrofuges when attached to carbon.
- Pauling, L.
- For compilations see: (a) McOmie, J. F. W. (Ed.), "Protective Groups in Organic Chemistry", Plenum, New York (1973); (b) Greene, T. W., "Protective Groups in Organic Synthesis, John Wiley & Sons, New York (1981).
- For reviews see: (a) Seebach, Dieter Angew. Chem. 1979 91, 259: (b) Aakermark, B.; Baeckvall, J. E.; Zetterberg, K. Acta Chem. Scand., Ser. B 1982 B36, 577.
- For a compilation see: Hase, T. A. (Ed.), "Umpoled Synthons", John Wiley & Sons, New Jersey (1987).
- Kaya, R.; Beller, N. R. J. Org. Chem. 1981 46, 196.
- Ross, N. C.; Levine, R. J. Org. Chem. 1964 29, 2341.