-
1
-
-
0001078311
-
-
For aldol additions of malonates in total synthesis of epolactaene, see
-
For aldol additions of malonates in total synthesis of epolactaene, see:, S. Marumoto, H. Kogen, S. Naruto, J. Org. Chem. 1998, 63, 2068-2069
-
(1998)
J. Org. Chem.
, vol.63
, pp. 2068-2069
-
-
Marumoto, S.1
Kogen, H.2
Naruto, S.3
-
2
-
-
0026733928
-
-
for aldol additions of malonates in the total synthesis of carbohydrates, see
-
for aldol additions of malonates in the total synthesis of carbohydrates, see:, A. Saba, V. Adovasio, M. Nardelli, Tetrahedron: Asymmetry 1992, 3, 1573-1582.
-
(1992)
Tetrahedron: Asymmetry
, vol.3
, pp. 1573-1582
-
-
Saba, A.1
Adovasio, V.2
Nardelli, M.3
-
3
-
-
20944434191
-
-
The failure of a planned aldol addition of substituted cyclohexane-1,3-dione in the total synthesis of coleophomones has been described, see
-
The failure of a planned aldol addition of substituted cyclohexane-1,3-dione in the total synthesis of coleophomones has been described, see:, K. C. Nicolaou, T. Montagnon, G. Vassilikogiannakis, C. J. N. Mathison, J. Am. Chem. Soc. 2005, 127, 8872-8888.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 8872-8888
-
-
Nicolaou, K.C.1
Montagnon, T.2
Vassilikogiannakis, G.3
Mathison, C.J.N.4
-
4
-
-
57849123842
-
-
For hydroxymethylation of 3-benzoyl-2-oxo-ethylpropionate, see
-
For hydroxymethylation of 3-benzoyl-2-oxo-ethylpropionate, see:, J. Couquelet, J. B. Boyer, J. Coquelet, Compt. Rend. S. Acad. Sciences, Ser. C: Sciences Chim. 1972, 274, 422-425
-
(1972)
Compt. Rend. S. Acad. Sciences, Ser. C: Sciences Chim.
, vol.274
, pp. 422-425
-
-
Couquelet, J.1
Boyer, J.B.2
Coquelet, J.3
-
5
-
-
78650359847
-
-
for use of acetoacetic ethyl ester in the presence of triethylamine, see:, German Patent DE 2336394
-
for use of acetoacetic ethyl ester in the presence of triethylamine, see:, J. W. Cornforth, J. E. Hawes, German Patent DE 2336394, 1974
-
(1974)
-
-
Cornforth, J.W.1
Hawes, J.E.2
-
6
-
-
27544468542
-
-
for hydroxymethylation of 2-oxocyclohexane- and 2- oxocyclopentanecarboxylic acid esters in the presence of CaO, see
-
for hydroxymethylation of 2-oxocyclohexane- and 2- oxocyclopentanecarboxylic acid esters in the presence of CaO, see:, H. Gerdes, H. Marschall, P. Weyerstahl, Chem. Ber. 1975, 108, 3448-3460
-
(1975)
Chem. Ber.
, vol.108
, pp. 3448-3460
-
-
Gerdes, H.1
Marschall, H.2
Weyerstahl, P.3
-
7
-
-
78650377058
-
-
for hydroxymethylation of 2.4-pentanedione in the presence of KOH, see:, European Patent EP 350320
-
for hydroxymethylation of 2.4-pentanedione in the presence of KOH, see:, J. J. Gyuran, European Patent EP 350320, 1990
-
(1990)
-
-
Gyuran, J.J.1
-
8
-
-
0030829742
-
-
for hydroxymethylation of malonates, see
-
for hydroxymethylation of malonates, see:, A. Guzaev, H. Lçnnberg, Synthesis 1997, 1281-1284
-
(1997)
Synthesis
, pp. 1281-1284
-
-
Guzaev, A.1
Lçnnberg, H.2
-
9
-
-
0032565996
-
-
for hydroxymethylation of α-methyl-substituted acetoacetic ethyl ester, see
-
for hydroxymethylation of α-methyl-substituted acetoacetic ethyl ester, see:, T. Akeboshi, Y. Ohtsuka, T. Sugai, H. Ohta, Tetrahedron 1998, 54, 7387-7394
-
(1998)
Tetrahedron
, vol.54
, pp. 7387-7394
-
-
Akeboshi, T.1
Ohtsuka, Y.2
Sugai, T.3
Ohta, H.4
-
10
-
-
34247228673
-
-
for iron-catalyzed hydroxymethylation, see
-
for iron-catalyzed hydroxymethylation, see:, C. Ogawa, S. Kobayashi, Chem. Lett. 2007, 36, 56-57.
-
(2007)
Chem. Lett.
, vol.36
, pp. 56-57
-
-
Ogawa, C.1
Kobayashi, S.2
-
11
-
-
78650411338
-
-
For aldol addition of formaldehyde to 1,3-dicarbonyl compounds used in the total syntheses of natural products, see
-
For aldol addition of formaldehyde to 1,3-dicarbonyl compounds used in the total syntheses of natural products, see
-
-
-
-
12
-
-
0026354213
-
-
Y. Tsuda, A. Ishiura, S. Takamura, S. Hosoi, K. Isobe, K. Mohri, Chem. Pharm. Bull. 1991, 39, 2797-2802
-
(1991)
Chem. Pharm. Bull.
, vol.39
, pp. 2797-2802
-
-
Tsuda, Y.1
Ishiura, A.2
Takamura, S.3
Hosoi, S.4
Isobe, K.5
Mohri, K.6
-
14
-
-
27544513455
-
-
For aldol addition of formaldehyde to activated ketones
-
For aldol addition of formaldehyde to activated ketones:, V. Lecomte, C. Bolm, Adv. Synth. Catal. 2005, 347, 1666-1672.
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1666-1672
-
-
Lecomte, V.1
Bolm, C.2
-
15
-
-
34547210299
-
-
For enantioselective aldol addition of formaldehyde in the presence of chiral palladium complexes, see
-
For enantioselective aldol addition of formaldehyde in the presence of chiral palladium complexes, see:, I. Fukuchi, Y. Hamashima, M. Sodeoka, Adv. Synth. Catal. 2007, 349, 509-512.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 509-512
-
-
Fukuchi, I.1
Hamashima, Y.2
Sodeoka, M.3
-
16
-
-
37749043974
-
-
For an aldol addition of aqueous formaldehyde with a bicyclic ß-keto ester, see
-
For an aldol addition of aqueous formaldehyde with a bicyclic ß-keto ester, see:, S. Shirakawa, S. Shimizu, Synlett 2007, 3160-3164.
-
(2007)
Synlett
, pp. 3160-3164
-
-
Shirakawa, S.1
Shimizu, S.2
-
18
-
-
2742554643
-
-
L. Birkofer, A. Ritter, H. Vernaleken, Chem. Ber. 1966, 99, 2518-2520
-
(1966)
Chem. Ber.
, vol.99
, pp. 2518-2520
-
-
Birkofer, L.1
Ritter, A.2
Vernaleken, H.3
-
25
-
-
33845278511
-
-
R. Antonioletti, F. Bonadies, A. Scettri, J. Org. Chem. 1988, 53, 5540-5542.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 5540-5542
-
-
Antonioletti, R.1
Bonadies, F.2
Scettri, A.3
-
26
-
-
57849161638
-
-
N. Umebayashi, Y. Hamashima, D. Hashizume, M. Sodeoka, Angew. Chem. 2008, 120, 4264-4267
-
(2008)
Angew. Chem.
, vol.120
, pp. 4264-4267
-
-
Umebayashi, N.1
Hamashima, Y.2
Hashizume, D.3
Sodeoka, M.4
-
27
-
-
53549115640
-
-
Angew. Chem. Int. Ed. 2008, 47, 4196-4199.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4196-4199
-
-
-
28
-
-
2442462280
-
-
D. J. Buchanan, D. J. Dixon, F. A. Hernandez-Juan, Org. Lett. 2004, 6, 1357-1360.
-
(2004)
Org. Lett.
, vol.6
, pp. 1357-1360
-
-
Buchanan, D.J.1
Dixon, D.J.2
Hernandez-Juan, F.A.3
-
29
-
-
19344375332
-
-
M. R. Acocella, M. De Rosa, A. Massa, L. Palombi, R. Villano, A. Scettri, Tetrahedron 2005, 61, 4091-4097
-
(2005)
Tetrahedron
, vol.61
, pp. 4091-4097
-
-
Acocella, M.R.1
De Rosa, M.2
Massa, A.3
Palombi, L.4
Villano, R.5
Scettri, A.6
-
30
-
-
33750510072
-
-
A. Scettri, M. R. Acocella, L. Palombi, C. Scalera, R. Villano, A. Massa, Adv. Synth. Catal. 2006, 348, 2229-2236
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 2229-2236
-
-
Scettri, A.1
Acocella, M.R.2
Palombi, L.3
Scalera, C.4
Villano, R.5
Massa, A.6
-
31
-
-
63849229103
-
-
x
-
A. Massa, V. de Sio, R. Villano, M. R. Acocella, L. Palombi, G. Sellitto, A. Peduto, R. Filosa, P. De Capraris, A. Scettri, Synthesis 2009, 0643-0649.x.
-
(2009)
Synthesis
, pp. 0643-0649
-
-
Massa, A.1
De Sio, V.2
Villano, R.3
Acocella, M.R.4
Palombi, L.5
Sellitto, G.6
Peduto, A.7
Filosa, R.8
De Capraris, P.9
Scettri, A.10
-
32
-
-
70449120031
-
-
A. Massa, A. Scettri, R. Filosa, L. Capozzolo, Tetrahedron Lett. 2009, 50, 7318-7321.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 7318-7321
-
-
Massa, A.1
Scettri, A.2
Filosa, R.3
Capozzolo, L.4
-
33
-
-
78650384420
-
-
For pioneering works about Lewis base activation of weak Lewis acids, see
-
For pioneering works about Lewis base activation of weak Lewis acids, see
-
-
-
-
34
-
-
15744387149
-
-
S. E. Denmark, G. L. Beutner, T. Winn, M. D. Eastgate, J. Am. Chem. Soc. 2005, 127, 3774-3789
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3774-3789
-
-
Denmark, S.E.1
Beutner, G.L.2
Winn, T.3
Eastgate, M.D.4
-
36
-
-
0037073229
-
-
S. E. Denmark, T. Winn, G. L. Beutner, J. Am. Chem. Soc. 2002, 124, 13405-13407
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 13405-13407
-
-
Denmark, S.E.1
Winn, T.2
Beutner, G.L.3
-
40
-
-
77956142428
-
-
A reversible cyclization of the hydroxy group with the cyano group of the aldol adduct could also explain the observed low reactivity (more details will be given in a future paper). For a recent reference about the formation of iminophthalanes and isoindolinones through a Henry reaction of o-cyanobenzaldehyde see
-
A reversible cyclization of the hydroxy group with the cyano group of the aldol adduct could also explain the observed low reactivity (more details will be given in a future paper). For a recent reference about the formation of iminophthalanes and isoindolinones through a Henry reaction of o-cyanobenzaldehyde see:, M. Angelin, M. Rahm, A. Fischer, T. Brinck, O. Ramstrom, J. Org. Chem. 2010, 75, 5882-5887.
-
(2010)
J. Org. Chem.
, vol.75
, pp. 5882-5887
-
-
Angelin, M.1
Rahm, M.2
Fischer, A.3
Brinck, T.4
Ramstrom, O.5
-
42
-
-
78650330157
-
-
For recent applications of trimethylchlorosilane as Lewis acid see
-
For recent applications of trimethylchlorosilane as Lewis acid see
-
-
-
-
44
-
-
70449123721
-
-
P. Wu, D. Lin, X. Lu, L. Zhou, J. Sun, Tetrahedron Lett. 2009, 50 7249-7251
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 7249-7251
-
-
Wu, P.1
Lin, D.2
Lu, X.3
Zhou, L.4
Sun, J.5
-
45
-
-
65249096668
-
-
V. Kysil, A. Khvat, S. Tsirulnikov, S. Tkachenko, A. Ivachtchenko, Tetrahedron Lett. 2009, 50, 2854-2856.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 2854-2856
-
-
Kysil, V.1
Khvat, A.2
Tsirulnikov, S.3
Tkachenko, S.4
Ivachtchenko, A.5
-
46
-
-
33947300284
-
-
For an early reference, see
-
For an early reference, see:, H. T. House, L. J. Czuba, M. Gall, H. Olmstead, J. Org. Chem. 1969, 34, 2324-2336.
-
(1969)
J. Org. Chem.
, vol.34
, pp. 2324-2336
-
-
House, H.T.1
Czuba, L.J.2
Gall, M.3
Olmstead, H.4
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