-
1
-
-
0035805264
-
-
See, for example
-
See, for example: (a) Nicolaou, K. C.; Mitchell, H. J. Angew. Chem., Int. Ed. 2001, 40, 1576-1624;
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 1576-1624
-
-
Nicolaou, K.C.1
Mitchell, H.J.2
-
2
-
-
0035022268
-
-
(b) Thorson, J. S.; Hosted, T. J., Jr.; Jiang, J.; Biggins, J. B.; Ahlert, J. Curr. Org. Chem. 2001, 5, 139-167;
-
(2001)
Curr. Org. Chem.
, vol.5
, pp. 139-167
-
-
Thorson, J.S.1
Hosted Jr., T.J.2
Jiang, J.3
Biggins, J.B.4
Ahlert, J.5
-
4
-
-
19944404265
-
-
See, for example
-
See, for example: (a) Werz, D. B.; Seeberger, P. H. Chem. Eur. J. 2005, 11, 3194-3206;
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 3194-3206
-
-
Werz, D.B.1
Seeberger, P.H.2
-
6
-
-
45349108661
-
-
(c) Carmona, A. T.; Moreno-Vargas, A. J.; Robina, I. Curr. Org. Chem. 2008, 5, 33-60.
-
(2008)
Curr. Org. Chem.
, vol.5
, pp. 33-60
-
-
Carmona, A.T.1
Moreno-Vargas, A.J.2
Robina, I.3
-
7
-
-
33748932220
-
-
See, for example: Osborn, H. M. I., Ed.; Academic Press-Elsevier: Oxford
-
See, for example: (a) Robertson, J.; Stafford, P. M. Carbohydrates In Osborn, H. M. I., Ed.; Academic Press-Elsevier: Oxford, 2003. pp 9-65;
-
(2003)
Carbohydrates
, pp. 9-65
-
-
Robertson, J.1
Stafford, P.M.2
-
10
-
-
0001569822
-
-
See, for example
-
See, for example: (a) Garegg, P. J. Acc. Chem. Res. 1992, 25, 575-580;
-
(1992)
Acc. Chem. Res.
, vol.25
, pp. 575-580
-
-
Garegg, P.J.1
-
12
-
-
77950355549
-
-
(c) Ekholm, F. S.; Sinkkonen, J.; Leino, R. New J. Chem. 2010, 34, 667-675.
-
(2010)
New J. Chem.
, vol.34
, pp. 667-675
-
-
Ekholm, F.S.1
Sinkkonen, J.2
Leino, R.3
-
13
-
-
0003405157
-
-
Thieme, Georg, Ed.; Verlag: Stuttgart
-
Kocieński, P. J. In Protecting Groups; Thieme, Georg, Ed.; Verlag: Stuttgart, 2005. Vol. 3, pp 137-155 and 241-257.
-
(2005)
Protecting Groups
, vol.3
-
-
Kocieński, P.J.1
-
14
-
-
8844269044
-
-
See for example
-
See for example: (a) Crich, D.; Banerjee, A.; Yao, Q. J. Am. Chem. Soc. 2004, 126, 14930-14934;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 14930-14934
-
-
Crich, D.1
Banerjee, A.2
Yao, Q.3
-
17
-
-
44449112869
-
-
Csajági, C.; Borcsek, B.; Niesz, K.; Kovács, I.; Székelyhidi, Z.; Bajkó, Z.; Ürge, L.; Darvas, F. Org. Lett. 2008, 10, 1589.
-
(2008)
Org. Lett.
, vol.10
, pp. 1589
-
-
Csajági, C.1
Borcsek, B.2
Niesz, K.3
Kovács, I.4
Székelyhidi, Z.5
Bajkó, Z.6
Ürge, L.7
Darvas, F.8
-
20
-
-
0034001616
-
-
For preparation and analytical data of compounds 1-4, see for example
-
For preparation and analytical data of compounds 1-4, see for example: (a) Tennant-Eyles, R. J.; Davis, B. G.; Fairbanks, A. J. Tetrahedron: Asymmetry 2000, 11, 231-243;
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 231-243
-
-
Tennant-Eyles, R.J.1
Davis, B.G.2
Fairbanks, A.J.3
-
21
-
-
34250812517
-
-
(b) El-Badri, M. H.; Willenbring, D.; Tantillo, D. J.; Gervay-Hague, J. J. Org. Chem. 2007, 72, 4663-4672;
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4663-4672
-
-
El-Badri, M.H.1
Willenbring, D.2
Tantillo, D.J.3
Gervay-Hague, J.4
-
24
-
-
0035858616
-
-
See, for example
-
See, for example: (a) Li, X.; Ohtake, H.; Ikegami, S.; Takahashi, H. Tetrahedron 2001, 57, 4283-4295;
-
(2001)
Tetrahedron
, vol.57
, pp. 4283-4295
-
-
Li, X.1
Ohtake, H.2
Ikegami, S.3
Takahashi, H.4
-
25
-
-
57249094148
-
-
(b) Perosa, A.; Tundo, P.; Zinovyev, S. Green Chem. 2002, 4, 492-494;
-
(2002)
Green Chem.
, vol.4
, pp. 492-494
-
-
Perosa, A.1
Tundo, P.2
Zinovyev, S.3
-
27
-
-
60849126676
-
-
See, for example
-
See, for example: (a) Poláková, M.; Roslund, M. U.; Ekholm, F. S.; Saloranta, T.; Leino, R. Eur. J. Org. Chem. 2009, 870-888;
-
(2009)
Eur. J. Org. Chem.
, pp. 870-888
-
-
Poláková, M.1
Roslund, M.U.2
Ekholm, F.S.3
Saloranta, T.4
Leino, R.5
-
28
-
-
33947475508
-
-
(b) Zderic, J. A.; Rivera, M. E. C.; Limón, D. C. J. Am. Chem. Soc. 1960, 82, 6373-6375.
-
(1960)
J. Am. Chem. Soc.
, vol.82
, pp. 6373-6375
-
-
Zderic, J.A.1
Rivera, M.E.C.2
Limón, D.C.3
-
29
-
-
0347416794
-
-
In a typical experimental setup, 20 mg of substrate was dissolved in 20 ml EtOAc:MeOH (1:1). The flow velocity was set with the HPLC pump to 1 ml/min. The hydrogen pressure was set to 40 bar, the temperature to 80 °C and a cartridge containing 10% Pd/C was utilized. After the reaction the sample was collected and evaporated to give the pure product. For analytical data on the products, see
-
In a typical experimental setup, 20 mg of substrate was dissolved in 20 ml EtOAc:MeOH (1:1). The flow velocity was set with the HPLC pump to 1 ml/min. The hydrogen pressure was set to 40 bar, the temperature to 80 °C and a cartridge containing 10% Pd/C was utilized. After the reaction the sample was collected and evaporated to give the pure product. For analytical data on the products, see: (a) Belakhov, V.; Dovgolevsky, E.; Rabkin, E.; Shulami, S.; Shoham, Y.; Baasov, T. Carbohydr. Res. 2004, 339, 385-392;
-
(2004)
Carbohydr. Res.
, vol.339
, pp. 385-392
-
-
Belakhov, V.1
Dovgolevsky, E.2
Rabkin, E.3
Shulami, S.4
Shoham, Y.5
Baasov, T.6
-
30
-
-
33748619237
-
-
(b) Horrobin, T.; Tran, C. H.; Crout, D. J. Chem. Soc., Perkin Trans. 1 1998, 1069-1080.
-
(1998)
J. Chem. Soc., Perkin Trans. 1
, pp. 1069-1080
-
-
Horrobin, T.1
Tran, C.H.2
Crout, D.3
|