-
8
-
-
0242656295
-
-
For a review of ynolate anions and siloxy alkynes, see:
-
For a review of ynolate anions and siloxy alkynes, see:. Shindo M. Synthesis (2003) 2275
-
(2003)
Synthesis
, pp. 2275
-
-
Shindo, M.1
-
9
-
-
0005941701
-
-
For a review of preparation and reactivity of alkoxy alkynes, see:. Raphael R.A., and Taylor E.C. (Eds), Interscience, New York, NY
-
For a review of preparation and reactivity of alkoxy alkynes, see:. Arens J.F. In: Raphael R.A., and Taylor E.C. (Eds). Advances in Organic Chemistry Methods and Results Vol. 2 (1960), Interscience, New York, NY 117-212
-
(1960)
Advances in Organic Chemistry Methods and Results
, vol.-2
, pp. 117-212
-
-
Arens, J.F.1
-
10
-
-
33750439735
-
-
Vieregge H., Schmidt H.M., Renema J., Bos H.J., and Arens J.F. Recueil 85 (1996) 929
-
(1996)
Recueil
, vol.85
, pp. 929
-
-
Vieregge, H.1
Schmidt, H.M.2
Renema, J.3
Bos, H.J.4
Arens, J.F.5
-
17
-
-
0003828015
-
-
Wiley, New York, NY
-
Tidwell T.T. Ketenes (1995), Wiley, New York, NY
-
(1995)
Ketenes
-
-
Tidwell, T.T.1
-
20
-
-
0141698480
-
-
Olah G.A., Alemayehu M., Wu A.H., Farooq O., and Prakash G.K.S. J. Am. Chem. Soc. 114 (1992) 8042
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 8042
-
-
Olah, G.A.1
Alemayehu, M.2
Wu, A.H.3
Farooq, O.4
Prakash, G.K.S.5
-
34
-
-
0000471716
-
-
For preparation of anhydrous tert-butyl hydroperoxide, see:
-
For preparation of anhydrous tert-butyl hydroperoxide, see:. Hill J.G., Rossiter B.E., and Sharpless K.B. J. Org. Chem. 48 (1983) 3607
-
(1983)
J. Org. Chem.
, vol.48
, pp. 3607
-
-
Hill, J.G.1
Rossiter, B.E.2
Sharpless, K.B.3
-
42
-
-
0347254810
-
-
Nishizawa M., Takao H., Yadav V.K., Imagawa H., and Sugihara T. Org. Lett. 5 (2003) 4563
-
(2003)
Org. Lett.
, vol.5
, pp. 4563
-
-
Nishizawa, M.1
Takao, H.2
Yadav, V.K.3
Imagawa, H.4
Sugihara, T.5
-
43
-
-
33750491018
-
-
2-promoted reactions, see:
-
-
-
-
49
-
-
18244388692
-
-
Zhang Y., Hsung R.P., Zhang X., Huang J., Slater B.W., and Davis A. Org. Lett. 7 (2005) 1047
-
(2005)
Org. Lett.
, vol.7
, pp. 1047
-
-
Zhang, Y.1
Hsung, R.P.2
Zhang, X.3
Huang, J.4
Slater, B.W.5
Davis, A.6
-
51
-
-
0003094929
-
-
Johnson W.S., Ward C.E., Boots S.G., Gravestock M.B., Markezich R.L., McCarry B.E., Okorie D.A., and Parry R.J. J. Am. Chem. Soc. 103 (1981) 88
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 88
-
-
Johnson, W.S.1
Ward, C.E.2
Boots, S.G.3
Gravestock, M.B.4
Markezich, R.L.5
McCarry, B.E.6
Okorie, D.A.7
Parry, R.J.8
-
52
-
-
0000960525
-
-
For other examples of halide abstraction from hydrocarbons by carbocations, see:
-
Balog A., Geib S.J., and Curran D.P. J. Org. Chem. 60 (1995) 345 For other examples of halide abstraction from hydrocarbons by carbocations, see:
-
(1995)
J. Org. Chem.
, vol.60
, pp. 345
-
-
Balog, A.1
Geib, S.J.2
Curran, D.P.3
-
54
-
-
33750465760
-
-
2O or AcOH is reversed (Ref. 14b). The acidity of the two acids in ionic liquid is comparable (Ref. 14c).
-
-
-
-
55
-
-
0011170266
-
-
Koppel I.A., Taft R.W., Anvia F., Zhu S., Hu L., Sung K., DesMarteau D.D., Yagupolskii L.M., Yagupolskii Y.L., Ignat'ev N.V., Kondratenko N.V., Volkonskii A.Y., Vlasov V.M., Notario R., and Maria P. J. Am. Chem. Soc. 116 (1994) 3047
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 3047
-
-
Koppel, I.A.1
Taft, R.W.2
Anvia, F.3
Zhu, S.4
Hu, L.5
Sung, K.6
DesMarteau, D.D.7
Yagupolskii, L.M.8
Yagupolskii, Y.L.9
Ignat'ev, N.V.10
Kondratenko, N.V.11
Volkonskii, A.Y.12
Vlasov, V.M.13
Notario, R.14
Maria, P.15
-
57
-
-
0037955598
-
-
Thomazeau C., Bourbigou H.O., Magna L., Luts S., and Gilbert B. J. Am. Chem. Soc. 125 (2003) 5264
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5264
-
-
Thomazeau, C.1
Bourbigou, H.O.2
Magna, L.3
Luts, S.4
Gilbert, B.5
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