-
1
-
-
0001095772
-
-
(a) Craig, T. W.; Harvey, G. R.; Berchtold, G. A. J. Org. Chem. 1967, 32, 3743-3749.
-
(1967)
J. Org. Chem.
, vol.32
, pp. 3743-3749
-
-
Craig, T.W.1
Harvey, G.R.2
Berchtold, G.A.3
-
2
-
-
0000096835
-
-
(b) Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Angew. Chem. Int. Ed. 2001, 40, 2004-2021.
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 2004-2021
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
3
-
-
34347360665
-
-
(c) Scheunemann, M.; Sorger, D.; Kouznetsova, E.; Sabri, O.; Schliebs, R.; Wenzel, B.; Steinbach, J. Tetrahedron Lett. 2007, 48, 5497-5501.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 5497-5501
-
-
Scheunemann, M.1
Sorger, D.2
Kouznetsova, E.3
Sabri, O.4
Schliebs, R.5
Wenzel, B.6
Steinbach, J.7
-
6
-
-
0342592514
-
-
(b) Gruber-Khadjawi, M.; Hönig, H.; Illaszewicz, C. Tetrahedron: Asymmetry 1996, 7, 807-814.
-
(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 807-814
-
-
Gruber-Khadjawi, M.1
Hönig, H.2
Illaszewicz, C.3
-
7
-
-
23844515192
-
-
(c) Clique, B.; Ironmonger, A.; Whittaker, B.; Colley, J.; Titchmarsh, J.; Stockley, P.; Nelson, A. Org. Biomol. Chem. 2005, 3, 2776-2785.
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 2776-2785
-
-
Clique, B.1
Ironmonger, A.2
Whittaker, B.3
Colley, J.4
Titchmarsh, J.5
Stockley, P.6
Nelson, A.7
-
8
-
-
23344434949
-
-
(d) Ironmonger, A.; Stockley, P.; Nelson, A. Org. Biomol. Chem. 2005, 3, 2350-2353.
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 2350-2353
-
-
Ironmonger, A.1
Stockley, P.2
Nelson, A.3
-
10
-
-
20344388819
-
-
(a) Narayan, S.; Muldoon, J.; Finn, M. G.; Fokin, V. V.; Kolb, H. C.; Sharpless, K. B. Angew. Chem. Int. Ed. 2005, 44, 3275-3279.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 3275-3279
-
-
Narayan, S.1
Muldoon, J.2
Finn, M.G.3
Fokin, V.V.4
Kolb, H.C.5
Sharpless, K.B.6
-
13
-
-
41849088108
-
-
(d) Wang, Z.; Cui, Y.-T.; Xu, Z.-B.; Qu, J. J. Org. Chem. 2008, 73, 2270-2274.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 2270-2274
-
-
Wang, Z.1
Cui, Y.-T.2
Xu, Z.-B.3
Qu, J.4
-
14
-
-
75749088634
-
Abstract of papers
-
Philadelphia, PA, August 17-21, 2008; American Chemical Society: Washington, DC MEDI-300
-
Carlier, P. R.; Monceaux, C. J.; Matsuoka, Y.; Hirate-Fukae, C. Abstract of Papers, 236th National Meeting of the American Chemical Society, Philadelphia, PA, August 17-21, 2008; American Chemical Society: Washington, DC, 2008; MEDI-300.
-
(2008)
236th National Meeting of the American Chemical Society
-
-
Carlier, P.R.1
Monceaux, C.J.2
Matsuoka, Y.3
Hirate-Fukae, C.4
-
16
-
-
75749104734
-
-
For example, cis-1,4-cyclohexadiene dioxide reacts with 2 equiv benzylamine 2a under neat reaction conditions to give only the 1,3-diol (see ref 1b, footnote 46)
-
For example, cis-1,4-cyclohexadiene dioxide reacts with 2 equiv benzylamine 2a under neat reaction conditions to give only the 1,3-diol (see ref 1b, footnote 46).
-
-
-
-
17
-
-
0037019976
-
-
(a) Serrano, P.; Llebaria, A.; Delgado, A. J. Org. Chem. 2002, 67, 7165-7167.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 7165-7167
-
-
Serrano, P.1
Llebaria, A.2
Delgado, A.3
-
18
-
-
22944475824
-
-
(b) Serrano, P.; Llebaria, A.; Vasquez, J.; de Pablo, J.; Anglada, J. A.; Delgado, A. Chem.-Eur. J. 2005, 11, 4465-4472.
-
(2005)
Chem.-Eur. J.
, vol.11
, pp. 4465-4472
-
-
Serrano, P.1
Llebaria, A.2
Vasquez, J.3
De Pablo, J.4
Anglada, J.A.5
Delgado, A.6
-
20
-
-
75749143549
-
-
As illustrative examples, in the case of entry 3, [1] = 2.1 M, [2e] = 8.3 M; for entry 6 [1] = 0.9 M, [2g] = 7.1 M (all reactants assumed to have density = 1 g/mL). These aniline concentrations are 7- to 8-fold higher than those employed in the acetonitrile, DMF, and mesitylene reactions described above
-
As illustrative examples, in the case of entry 3, [1] = 2.1 M, [2e] = 8.3 M; for entry 6 [1] = 0.9 M, [2g] = 7.1 M (all reactants assumed to have density = 1 g/mL). These aniline concentrations are 7- to 8-fold higher than those employed in the acetonitrile, DMF, and mesitylene reactions described above.
-
-
-
-
21
-
-
75749117613
-
-
Autocatalysis in epoxide ring-opening under neat conditions has been proposed by Sharpless and co-workers (refs lb, 5a)
-
Autocatalysis in epoxide ring-opening under neat conditions has been proposed by Sharpless and co-workers (refs lb, 5a).
-
-
-
-
22
-
-
42749093497
-
-
Note, however, that this effect can explain some of the results observed in: Kiss, L.; Forró, E.; Martinek, T. A.; Bernáth, G.; De Kimpe, N.; Fülöp, F. Tetrahedron 2008, 64, 5036-5043.
-
(2008)
Tetrahedron
, vol.64
, pp. 5036-5043
-
-
Kiss, L.1
Forró, E.2
Martinek, T.A.3
Bernáth, G.4
De Kimpe, N.5
Fülöp, F.6
|