-
1
-
-
50249134990
-
Lewis base catalysis in organic synthesis
-
Reviews
-
Reviews:, Denmark SE, Beutner GL,. Lewis base catalysis in organic synthesis. Angew Chem Int Ed 2008; 47: 1560-638.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 1560-1638
-
-
Denmark, S.E.1
Beutner, G.L.2
-
2
-
-
39649097831
-
Steroselective reactions involving hypervalent silicate complexes
-
Benaglia M, Guizzetti S, Pignataro L,. Steroselective reactions involving hypervalent silicate complexes. Coord Chem Rev 2008; 252: 492-512.
-
(2008)
Coord Chem Rev
, vol.252
, pp. 492-512
-
-
Benaglia, M.1
Guizzetti, S.2
Pignataro, L.3
-
3
-
-
84883859229
-
Silicate-mediated stereoselective reactions catalyzed by chiral Lewis bases
-
Hoboken, NJ: John Wiley & Sons;. p
-
Benaglia M, Guizzetti S, Rossi S,. Silicate-mediated stereoselective reactions catalyzed by chiral Lewis bases. In: Catalytic methods in asymmetric synthesis. Hoboken, NJ: John Wiley & Sons; 2011. p 579-624.
-
(2011)
Catalytic Methods in Asymmetric Synthesis
, pp. 579-624
-
-
Benaglia, M.1
Guizzetti, S.2
Rossi, S.3
-
4
-
-
0033935920
-
Asymmetric catalysis of aldol reactions with chiral Lewis bases
-
Denmark SE, Stavenger RA,. Asymmetric catalysis of aldol reactions with chiral Lewis bases. Acc Chem Res 2000; 33: 432-440.
-
(2000)
Acc Chem Res
, vol.33
, pp. 432-440
-
-
Denmark, S.E.1
Stavenger, R.A.2
-
5
-
-
69049110960
-
On the mechanism of Lewis base catalyzed aldol addition reactions: Kinetic and spectroscopic investigations using rapid-injection NMR
-
For more recent contributions see ref. 3 and,: and references cited
-
For more recent contributions see ref. 3 and, Denmark SE, Eklov BM, Yao PJ, Eastgate MD,. On the mechanism of Lewis base catalyzed aldol addition reactions: kinetic and spectroscopic investigations using rapid-injection NMR. J Am Chem Soc 2009; 131: 11770-11787 and references cited.
-
(2009)
J Am Chem Soc
, vol.131
, pp. 11770-11787
-
-
Denmark, S.E.1
Eklov, B.M.2
Yao, P.J.3
Eastgate, M.D.4
-
6
-
-
78650397752
-
Trimethylchlorosilane and silicon tetrachloride in two novel methodologies for the efficient and mild aldol addition of β-keto esters and malonates to aldehydes
-
See also:,: and references cited
-
See also:, Massa A, Roscigno A, De Caprariis P, Filosa R, Di Mola A,. Trimethylchlorosilane and silicon tetrachloride in two novel methodologies for the efficient and mild aldol addition of β-keto esters and malonates to aldehydes. Adv Synth Catal 2010; 352: 3348-3354 and references cited.
-
(2010)
Adv Synth Catal
, vol.352
, pp. 3348-3354
-
-
Massa, A.1
Roscigno, A.2
De Caprariis, P.3
Filosa, R.4
Di Mola, A.5
-
7
-
-
77955502679
-
Chiral phosphine oxides in present-day organocatalysis
-
Rossi S, Benaglia M,. Chiral phosphine oxides in present-day organocatalysis. Org Biomol Chem 2010; 8: 3824-3830.
-
(2010)
Org Biomol Chem
, vol.8
, pp. 3824-3830
-
-
Rossi, S.1
Benaglia, M.2
-
8
-
-
33847632961
-
Chiral phosphine oxide BINAPO as a Lewis base catalyst for asymmetric allylation and aldol reaction of trichlorosilyl compounds
-
Kotani S, Hashimoto S, Nakajima M,. Chiral phosphine oxide BINAPO as a Lewis base catalyst for asymmetric allylation and aldol reaction of trichlorosilyl compounds. Tetrahedron 2007; 63: 3122-3132.
-
(2007)
Tetrahedron
, vol.63
, pp. 3122-3132
-
-
Kotani, S.1
Hashimoto, S.2
Nakajima, M.3
-
9
-
-
52649107590
-
Lewis base-catalyzed conjugate reduction and reductive aldol reaction of α,β-unsaturated ketones using trichlorosilane
-
Sugiura M, Sato N, Kotani S, Nakajima M,. Lewis base-catalyzed conjugate reduction and reductive aldol reaction of α,β-unsaturated ketones using trichlorosilane. Chem Commun 2008; 0: 4309-4311.
-
(2008)
Chem Commun
, vol.0
, pp. 4309-4311
-
-
Sugiura, M.1
Sato, N.2
Kotani, S.3
Nakajima, M.4
-
10
-
-
67650573256
-
Asymmetric synthesis of 4H-1,3-oxazines: Enantioselective reductive cyclization of N-acylated β-amino enones with trichlorosilane catalyzed by chiral Lewis bases
-
Sugiura M, Kumahara M, Nakajima M,. Asymmetric synthesis of 4H-1,3-oxazines: enantioselective reductive cyclization of N-acylated β-amino enones with trichlorosilane catalyzed by chiral Lewis bases. Chem Commun 2009; 0: 3585-3587.
-
(2009)
Chem Commun
, vol.0
, pp. 3585-3587
-
-
Sugiura, M.1
Kumahara, M.2
Nakajima, M.3
-
11
-
-
67449088256
-
Novel enantioselective direct aldol-type reaction promoted by a chiral phosphine oxide as an organocatalyst
-
Kotani S, Shimoda Y, Sugiura M, Nakajima M,. Novel enantioselective direct aldol-type reaction promoted by a chiral phosphine oxide as an organocatalyst. Tetrahedron Lett 2009; 50: 4602-4605.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 4602-4605
-
-
Kotani, S.1
Shimoda, Y.2
Sugiura, M.3
Nakajima, M.4
-
12
-
-
77749296044
-
Diastereo- and enantioselective reductive aldol reaction with trichlorosilane using chiral Lewis bases as organocatalysts
-
Sugiura M, Sato N, Sonoda Y, Kotani S, Nakajima M,. Diastereo- and enantioselective reductive aldol reaction with trichlorosilane using chiral Lewis bases as organocatalysts. Chem Asian J 2010; 5: 478-481.
-
(2010)
Chem Asian J
, vol.5
, pp. 478-481
-
-
Sugiura, M.1
Sato, N.2
Sonoda, Y.3
Kotani, S.4
Nakajima, M.5
-
13
-
-
84863613652
-
Enantioselective reductive aldol reaction using tertiary amine as hydride donor
-
Osakama K, Sugiura M, Nakajima, M, Kotani S,. Enantioselective reductive aldol reaction using tertiary amine as hydride donor. Tetrahedron Lett 2012; 53: 4199-4201.
-
(2012)
Tetrahedron Lett
, vol.53
, pp. 4199-4201
-
-
Osakama, K.1
Sugiura, M.2
Nakajima, M.3
Kotani, S.4
-
14
-
-
84861614700
-
Trichlorosilyl triflate-mediated enantioselective directed cross-aldol reaction between ketones using a chiral phosphine oxide as an organocatalyst
-
Aoki S, Kotani S, Sugiura M, Nakajima M,. Trichlorosilyl triflate-mediated enantioselective directed cross-aldol reaction between ketones using a chiral phosphine oxide as an organocatalyst. Chem Commun 2012; 48: 5524-5526.
-
(2012)
Chem Commun
, vol.48
, pp. 5524-5526
-
-
Aoki, S.1
Kotani, S.2
Sugiura, M.3
Nakajima, M.4
-
15
-
-
79955378501
-
Organocatalytic stereoselective direct aldol reaction of trifluoroethyl thioesters
-
Rossi S, Benaglia M, Cozzi F, Genoni A, Benincori T,. Organocatalytic stereoselective direct aldol reaction of trifluoroethyl thioesters. Adv Synth Catal 2011; 353: 848-854.
-
(2011)
Adv Synth Catal
, vol.353
, pp. 848-854
-
-
Rossi, S.1
Benaglia, M.2
Cozzi, F.3
Genoni, A.4
Benincori, T.5
-
16
-
-
78649790892
-
Biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol reactions
-
Rossi S, Benaglia M, Genoni A, Benincori T, Celentano G,. Biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol reactions. Tetrahedron 2011; 67: 158-166.
-
(2011)
Tetrahedron
, vol.67
, pp. 158-166
-
-
Rossi, S.1
Benaglia, M.2
Genoni, A.3
Benincori, T.4
Celentano, G.5
-
17
-
-
84865064701
-
Readily available (S)-proline-derived organocatalysts for the Lewis acid-mediated Lewis base-catalyzed stereoselective aldol reactions of activated thioesters
-
Bonsignore M, Benaglia M, Cozzi F, Genoni A, Rossi S, Raimondi L,. Readily available (S)-proline-derived organocatalysts for the Lewis acid-mediated Lewis base-catalyzed stereoselective aldol reactions of activated thioesters. Tetrahedron 2012; 68: 8251-8255.
-
(2012)
Tetrahedron
, vol.68
, pp. 8251-8255
-
-
Bonsignore, M.1
Benaglia, M.2
Cozzi, F.3
Genoni, A.4
Rossi, S.5
Raimondi, L.6
-
18
-
-
79959962212
-
Enantioselective double aldol reaction catalyzed by chiral phosphine oxide
-
Shimoda Y, Kotani S, Sugiura M, Nakajima M,. Enantioselective double aldol reaction catalyzed by chiral phosphine oxide. Chem Eur J 2011; 17: 7992-7995.
-
(2011)
Chem Eur J
, vol.17
, pp. 7992-7995
-
-
Shimoda, Y.1
Kotani, S.2
Sugiura, M.3
Nakajima, M.4
-
19
-
-
38349100690
-
Asymmetric enamine catalysis
-
For recent review on direct aldol reactions see
-
For recent review on direct aldol reactions see:, Mukherjee S, Yang JW, Hoffmann S, List B,. Asymmetric enamine catalysis. Chem Rev 2007; 107: 5471-5569.
-
(2007)
Chem Rev
, vol.107
, pp. 5471-5569
-
-
Mukherjee, S.1
Yang, J.W.2
Hoffmann, S.3
List, B.4
-
20
-
-
84857258027
-
Recent developments in asymmetric organocatalytic domino reactions
-
For a recent review on domino reactions see:
-
For a recent review on domino reactions see:, Pellisier H,. Recent developments in asymmetric organocatalytic domino reactions. Adv Synth Catal 2012; 354: 237-294.
-
(2012)
Adv Synth Catal
, vol.354
, pp. 237-294
-
-
Pellisier, H.1
-
21
-
-
53849127182
-
Novel chiral biheteroaromatic diphosphine oxides for Lewis base activation of Lewis acids in enantioselective allylation and epoxide opening
-
See ref. 15-17 and
-
See ref. 15-17 and, Simonini V, Benaglia M, Benincori T,. Novel chiral biheteroaromatic diphosphine oxides for Lewis base activation of Lewis acids in enantioselective allylation and epoxide opening. Adv Synth Catal 2008; 350: 561-564.
-
(2008)
Adv Synth Catal
, vol.350
, pp. 561-564
-
-
Simonini, V.1
Benaglia, M.2
Benincori, T.3
|