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1
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0003417469
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Pergamon: Oxford
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(a) Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Schreiber, S. L., Eds.; Pergamon: Oxford, 1991; pp 761-773.
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(1991)
Comprehensive Organic Synthesis
, pp. 761-773
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Trost, B.M.1
Fleming, I.2
Schreiber, S.L.3
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4
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0000826482
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Kurihara, N.; Miyamoto, J.; Paulson, G. D.; Zeeh, B.; Skidmore, M. W.; Hollingworth, R. M.; Kuiper, H. A. Pure Appl. Chem. 1997, 69, 2007-2025.
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(1997)
Pure Appl. Chem.
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Kurihara, N.1
Miyamoto, J.2
Paulson, G.D.3
Zeeh, B.4
Skidmore, M.W.5
Hollingworth, R.M.6
Kuiper, H.A.7
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5
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37049089790
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See for example: Mitchell, A. G.; Nicolls, D.; Walker, I.; Irwin, W. J.; Freeman, S. J. Chem. Soc., Perkins Trans. 2 1991, 1297-1303
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(1991)
J. Chem. Soc., Perkins Trans. 2
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Mitchell, A.G.1
Nicolls, D.2
Walker, I.3
Irwin, W.J.4
Freeman, S.5
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7
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0026502971
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Jouko, V.; Heikki, N.; Esko, P. Synth. Commun. 1992, 22, 271-276.
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(1992)
Synth. Commun.
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, pp. 271-276
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Jouko, V.1
Heikki, N.2
Esko, P.3
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9
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0040564847
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For a variety of alternative phosphonate synthetic techniques see, for example: (a) Tuong, par N. T.; Convert, F.; Martin, G.; Chabrier, P. Bull. Soc. Chem. Fr. 1965, 1925-1930.
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(1965)
Bull. Soc. Chem. Fr.
, pp. 1925-1930
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Par Tuong, N.T.1
Convert, F.2
Martin, G.3
Chabrier, P.4
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11
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4243926603
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Georg Thieme Verlag: Stuttgart, Germany
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(c) Müller, E. Methoden Der Organischen Chemie; Georg Thieme Verlag: Stuttgart, Germany, 1963; Vol. 12, pp 387-420.
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(1963)
Methoden Der Organischen Chemie
, vol.12
, pp. 387-420
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Müller, E.1
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13
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0031801212
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(b) Stanton, M. G.; Allen C. B.; Kissling, R. M.; Lincoln, A. L.; Gagné, M. R. J. Am. Chem. Soc. 1998, 120, 5981-5989.
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(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 5981-5989
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Stanton, M.G.1
Allen, C.B.2
Kissling, R.M.3
Lincoln, A.L.4
Gagné, M.R.5
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15
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0344007187
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note
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Dimethyl phenylphosphonate was found to behave similarly, in fact, giving slightly higher rates than DMMP.
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16
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0344438472
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note
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This estimate does not take into account the extra turnovers required to convert methyl ethyl methylphosphonate to diethyl methylphosphonate.
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17
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0344870308
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note
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Some THF was necessary for reactivity as reactions carried out in neat tBuOAc were sluggish.
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18
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0003942864
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John Wiley & Sons: New York, Chapter 10
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Since IMMP is chiral, it therefore has an additional contribution to its entropy equal to R In 2, the entropy of mixing. See: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; John Wiley & Sons: New York, 1994; Chapter 10, p 601.
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(1994)
Stereochemistry of Organic Compounds
, pp. 601
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Eliel, E.L.1
Wilen, S.H.2
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19
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0029525278
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Pregel, M, J.; Dunn, E. J.; Nagelkerke, R.; Thatcher, G. R J.; Buncel, E. Chem. Soc. Rev. 1995, 449-455.
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(1995)
Chem. Soc. Rev.
, pp. 449-455
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Pregel, M.J.1
Dunn, E.J.2
Nagelkerke, R.3
Thatcher, G.R.J.4
Buncel, E.5
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21
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0000562789
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(b) Jackman, L. M.; Petrei, M. M.; Smith, B. D. J. J. Am. Chem. Soc. 1991, 113, 3451-3458.
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(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 3451-3458
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Jackman, L.M.1
Petrei, M.M.2
Smith, B.D.J.3
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22
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84981790880
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Since NaOMe is an insoluble sheetlike material, the catalyst is most reasonably in a solubilized form: (a) Weiss, von E.; Alsdorf, H. Z. Anorg. Chem. 1970, 372, 206-213.
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(1970)
Z. Anorg. Chem.
, vol.372
, pp. 206-213
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Von Weiss, E.1
Alsdorf, H.2
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24
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5244370033
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Pangborn, A. B.; Giardello, M. A.; Grubbs, R. H.; Rosen, R. K.; Timmers, F. J. Organometallics 1996, 15, 1518-1520.
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(1996)
Organometallics
, vol.15
, pp. 1518-1520
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Pangborn, A.B.1
Giardello, M.A.2
Grubbs, R.H.3
Rosen, R.K.4
Timmers, F.J.5
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