-
1
-
-
55949092663
-
-
J. C. Anderson, A. J. Blake. M. Mills, P. D. Ratcliffe, Org. Lett. 2008, 10, 4141-4143.
-
(2008)
Org. Lett.
, vol.10
, pp. 4141-4143
-
-
Anderson, J.C.1
Blake, A.J.2
Mills, M.3
Ratcliffe, P.D.4
-
3
-
-
64149095419
-
-
1.3-Dipolar cycloaddilions: a (Ed.: A. Hassner), Springer, Berlin
-
Dipolar cycloaddilions: a) I. N. N. Namboothiri. N. Rastogi in Isoxazolines from Nitro Compounds: Synthesis and Applications, Vol. 12 (Ed.: A. Hassner), Springer, Berlin, 2008, pp. 1-44;
-
(2008)
Isoxazolines from Nitro Compounds: Synthesis and Applications
, vol.12
, pp. 1-44
-
-
Namboothiri, I.N.N.1
Rastogi, N.2
-
4
-
-
77954333597
-
-
(Eds.: A. Padwa, W. H. Pearson), Wiley, New York, Chapter 2; Henry reaction
-
b) S. E.Denmark, J. J. Cottel in The Chemistry of Heterocyclic Compounds, Vol. 59: Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products (Eds.: A. Padwa, W. H. Pearson), Wiley, New York, 2002, Chapter 2; Henry reaction:
-
(2002)
The Chemistry of Heterocyclic Compounds, Vol. 59: Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
-
-
E.Denmark, S.1
Cottel, J.J.2
-
6
-
-
0041365865
-
-
d) T. Ooi, K. Doda, K. Maruoka, J. Am. Chem. Soc. 2003, 125, 9022-9023;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 9022-9023
-
-
Ooi, T.1
Doda, K.2
Maruoka, K.3
-
7
-
-
28644434112
-
-
e) T. Ooi, K. Doda, S. Takada, K. Maruoka, Tetrahedron Lett. 2006, 47,145-148;
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 145-148
-
-
Ooi, T.1
Doda, K.2
Takada, S.3
Maruoka, K.4
-
8
-
-
34250659766
-
-
f) T. Ooi, S. Takada, K. Doda, K. Maruoka, Angew. Chem. 2006, 118, 7768-7770;
-
(2006)
Angew. Chem.
, vol.118
, pp. 7768-7770
-
-
Ooi, T.1
Takada, S.2
Doda, K.3
Maruoka, K.4
-
9
-
-
33845202019
-
-
Angew. Chem. Int. Ed. 2006, 45, 7606-7608.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7606-7608
-
-
-
10
-
-
61949457358
-
-
For a recent review on the activation of TMSCN by bases, see
-
For a recent review on the activation of TMSCN by bases, see: J. Gawronski, N. Wascinska, J. Gajewy, Chem. Rev. 2008, 108, 5227-5252.
-
(2008)
Chem. Rev.
, vol.108
, pp. 5227-5252
-
-
Gawronski, J.1
Wascinska, N.2
Gajewy, J.3
-
11
-
-
38349135345
-
-
For reviews concerning bifunctional thiourea organocatalysis, see: a
-
For reviews concerning bifunctional thiourea organocatalysis, see: a) A.G. Doyle, E.N. Jacobsen, Chem. Rev. 2007, 107, 5713-5743;
-
(2007)
Chem. Rev.
, vol.107
, pp. 5713-5743
-
-
Doyle, A.G.1
Jacobsen, E.N.2
-
14
-
-
33646468489
-
-
Angew. Chem. Int. Ed. 2006, 45, 1520-1543;
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 1520-1543
-
-
-
16
-
-
70349617279
-
-
e) P. S. Bhadury, B.-A. Song, S. Yang, D.-Y. Hu, W. Xue, Curr. Org. Synth. 2009, 6, 380-399.
-
(2009)
Curr. Org. Synth.
, vol.6
, pp. 380-399
-
-
Bhadury, P.S.1
Song, B.-A.2
Yang, S.3
Hu, D.-Y.4
Xue, W.5
-
17
-
-
19544393388
-
-
B. Vakulya, S. Varga, A. Csámpai, T. Soós, Org. Lett. 2005, 7, 1967-1969.
-
(2005)
Org. Lett.
, vol.7
, pp. 1967-1969
-
-
Vakulya, B.1
Varga, S.2
Csámpai, A.3
Soós, T.4
-
18
-
-
33746212557
-
-
T. Marcelli, R. N. S. van der Haas, J. H. van Maar-seveen, H. Hiemstra, Angew. Chem,. 2006, 118, 943-945;
-
(2006)
Angew. Chem,.
, vol.118
, pp. 943-945
-
-
Marcelli, T.1
Van Der Haas, R.N.S.2
Van Maar-seveen, J.H.3
Hiemstra, H.4
-
20
-
-
34250659766
-
-
T. Ooi, S. Takada, K. Doda, K. Maruoka, Angew. Chem. 2006, 118, 7768-7770;
-
(2006)
Angew. Chem.
, vol.118
, pp. 7768-7770
-
-
Ooi, T.1
Takada, S.2
Doda, K.3
Maruoka, K.4
-
21
-
-
33845202019
-
-
Angew. Chem. Int. Ed. 2006, 45, 7606-7608.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7606-7608
-
-
-
22
-
-
77954317467
-
-
Reactions of 7 with conventional, alkylating reagents resulted in the undesired alkylation of the thiourea sulfur atom.
-
Reactions of 7 with conventional, alkylating reagents resulted in the undesired alkylation of the thiourea sulfur atom.
-
-
-
-
23
-
-
77954344713
-
-
The reaction using β-nitrostyrene as representative of aromatic substrates was unsuccessfully investigated.
-
The reaction using β-nitrostyrene as representative of aromatic substrates was unsuccessfully investigated.
-
-
-
-
24
-
-
0030068354
-
-
D. Enders, R. Syrig, G. Raabe, R. Fernández, J. M. Lassaletta, J. M. Llera, Synthesis 1996, 48-52.
-
(1996)
Synthesis
, pp. 48-52
-
-
Enders, D.1
Syrig, R.2
Raabe, G.3
Fernández, R.4
Lassaletta, J.M.5
Llera, J.M.6
-
25
-
-
37349098707
-
-
P. Hammar, T. Marcelli, H. Hiemstra, F. Himo, Adv. Synth. Catal. 2007, 549, 2537-2548.
-
(2007)
Adv. Synth. Catal.
, vol.549
, pp. 2537-2548
-
-
Hammar, P.1
Marcelli, T.2
Hiemstra, H.3
Himo, F.4
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