-
3
-
-
33748247006
-
-
Noyori, R.; Kitamura, M. Angew. Chem., Int. Ed. Engl. 1991, 30, 49-69.
-
(1991)
Angew. Chem., Int. Ed. Engl.
, vol.30
, pp. 49-69
-
-
Noyori, R.1
Kitamura, M.2
-
4
-
-
15444369094
-
-
(a) Braga, A. L.; Alves, E.; Silveira, C.; Zeni, G.; Appell, H.; Wessjohan, L. Synthesis 2005, 588-594.
-
(2005)
Synthesis
, pp. 588-594
-
-
Braga, A.L.1
Alves, E.2
Silveira, C.3
Zeni, G.4
Appell, H.5
Wessjohan, L.6
-
6
-
-
0141631574
-
-
Braga, A. L.; Paixao, M. W.; Ludtke, D. S.; Silveira, C. C.; Rodrigues, O. E. D. Org. Lett. 2003, 5, 2635-2638.
-
(2003)
Org. Lett.
, vol.5
, pp. 2635-2638
-
-
Braga, A.L.1
Paixao, M.W.2
Ludtke, D.S.3
Silveira, C.C.4
Rodrigues, O.E.D.5
-
8
-
-
17444375310
-
-
(a) Vastila, P.; Pastor, I. M.; Adolfsson, H. J. Org. Chem. 2005, 70, 2921-2929.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 2921-2929
-
-
Vastila, P.1
Pastor, I.M.2
Adolfsson, H.3
-
9
-
-
10844234849
-
-
(b) Mao, J.; Wan, B.; Wang, R.; Wu, F.; Lu, S. J. Org. Chem. 2004, 69, 9123-9127.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 9123-9127
-
-
Mao, J.1
Wan, B.2
Wang, R.3
Wu, F.4
Lu, S.5
-
10
-
-
27644550057
-
-
2Zn, see: (a) Wieland, L. C.; Deng, H.; Snapper, M. L.; Hoveyda, A. H. J. Am. Chem. Soc. 2005, 127, 15453-15456.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15453-15456
-
-
Wieland, L.C.1
Deng, H.2
Snapper, M.L.3
Hoveyda, A.H.4
-
11
-
-
20444422576
-
-
(b) Blay, G.; Fernàndez, I.; Hernàndez-Olmos, V.; Marco-Aleixandre, A.; Pedro, J. R. Tetrahedron: Asymmetry 2005, 16, 1953-1958.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 1953-1958
-
-
Blay, G.1
Fernàndez, I.2
Hernàndez-Olmos, V.3
Marco-Aleixandre, A.4
Pedro, J.R.5
-
12
-
-
6444226688
-
-
(c) Lurain, A. E.; Maestri, A.; Kelly, A. R.; Carroll, P. J.; Walsh, P. J. J. Am. Chem. Soc. 2004, 126, 13608-13609.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13608-13609
-
-
Lurain, A.E.1
Maestri, A.2
Kelly, A.R.3
Carroll, P.J.4
Walsh, P.J.5
-
13
-
-
3142636801
-
-
(d) García-Delgado, N.; Fontes, M.; Pericàs, M. A.; Riera, A.; Verdaguer, X. Tetrahedron: Asymmetry 2004, 15, 2085-2090.
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 2085-2090
-
-
García-Delgado, N.1
Fontes, M.2
Pericàs, M.A.3
Riera, A.4
Verdaguer, X.5
-
14
-
-
4644274423
-
-
(e) Sprout, C. M.; Richmond, M. L.; Seto, C. T. J. Org. Chem. 2004, 69, 6666-6673.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 6666-6673
-
-
Sprout, C.M.1
Richmond, M.L.2
Seto, C.T.3
-
16
-
-
0040514974
-
-
Kitamura, M.; Okada, S.; Suga, S.; Noyori, R. J. Am. Chem. Soc. 1989, 111, 4028-4036.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 4028-4036
-
-
Kitamura, M.1
Okada, S.2
Suga, S.3
Noyori, R.4
-
23
-
-
0030600186
-
-
Cozzi, P. G.; Papa, A.; Umani-Ronchi, A. Tetrahedron Lett. 1996, 37, 4613-4616.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4613-4616
-
-
Cozzi, P.G.1
Papa, A.2
Umani-Ronchi, A.3
-
24
-
-
20444435525
-
-
(a) Fennie, M. W.; DiMauro, E. F.; O'Brien, E. M.; Annamalai, V.; Kozlowski, M. C. Tetrahedron 2005, 61, 6249-6265.
-
(2005)
Tetrahedron
, vol.61
, pp. 6249-6265
-
-
Fennie, M.W.1
Dimauro, E.F.2
O'Brien, E.M.3
Annamalai, V.4
Kozlowski, M.C.5
-
29
-
-
25144436523
-
-
(c) Jarvo, E. R.; Lawrence, B. M.; Jacobsen, E. N. Angew. Chem., Int. Ed. 2005, 44, 6043-6046.
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 6043-6046
-
-
Jarvo, E.R.1
Lawrence, B.M.2
Jacobsen, E.N.3
-
31
-
-
22144446027
-
-
2Zn can be used as deprotonating agent in alkynylation, due to its lower reactivity towards aldehydes: Cozzi, P. G.; Rudolph, J.; Bolm, C.; Norrby, P.-O.; Tomasini, C. J. Org. Chem. 2005, 70, 5733-5736.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 5733-5736
-
-
Cozzi, P.G.1
Rudolph, J.2
Bolm, C.3
Norrby, P.-O.4
Tomasini, C.5
-
32
-
-
28544452446
-
-
An important green chemistry approach to more efficient asymmetric reactions was reported by Walsh, see: Jeon, S.-J.; Li, H.; Walsh, P. J. J. Am. Chem. Soc. 2005, 127, 16416-16425.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 16416-16425
-
-
Jeon, S.-J.1
Li, H.2
Walsh, P.J.3
-
33
-
-
33646151103
-
-
note
-
Linear aliphatic aldehydes were also tested; Hydrocinnamic aldehyde gives 86% ee, and octanal gives 81% ee. With cyclohexanecarboxaldehyde (Table 2, entry 12, 68% yield) only unreacted aldehyde and the desired product were observed by GC/MS and TLC after quenching.
-
-
-
-
34
-
-
17644399859
-
-
2, see: Biswas, K.; Priera, O.; Goldsmith, P. J.; Woodward, S. Angew. Chem., Int. Ed. 2005, 44, 2232-2334.
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 2232-2334
-
-
Biswas, K.1
Priera, O.2
Goldsmith, P.J.3
Woodward, S.4
|