-
2
-
-
2742606973
-
Transition-metal catalysis of the Michael reaction of 1,3-dicarbonyl compounds and acceptor-activated alkenes
-
For a review, see: Christoffers J. Transition-metal catalysis of the Michael reaction of 1,3-dicarbonyl compounds and acceptor-activated alkenes. Eur J Org Chem 1998;10:1259-1266.
-
(1998)
Eur J Org Chem
, vol.10
, pp. 1259-1266
-
-
Christoffers, J.1
-
4
-
-
0034740372
-
Recent developments in lanthanide mediated organic synthesis
-
Steel PG. Recent developments in lanthanide mediated organic synthesis. J Chem Soc Perkin Trans 1 2001;2727-2751.
-
(2001)
J Chem Soc Perkin Trans 1
, pp. 2727-2751
-
-
Steel, P.G.1
-
5
-
-
0035126119
-
Recent advances in catalytic enantioselective Michael additions
-
Krause N, Hoffann-Roder A. Recent advances in catalytic enantioselective Michael additions. Synthesis 2001;171-196.
-
(2001)
Synthesis
, pp. 171-196
-
-
Krause, N.1
Hoffann-Roder, A.2
-
6
-
-
0034612973
-
Enantioselective conjugate additions
-
Sibi MP, Manyem S. Enantioselective conjugate additions. Tetrahedron 2000;56:8033-8061.
-
(2000)
Tetrahedron
, vol.56
, pp. 8033-8061
-
-
Sibi, M.P.1
Manyem, S.2
-
7
-
-
0000679263
-
Conjugate addition of organometallic reagents
-
Jacobsen EN, Pfaltz A, Yamamoto H, editors. Berlin: Springer
-
Tomioka K, Nagaoka Y. Conjugate addition of organometallic reagents. In: Jacobsen EN, Pfaltz A, Yamamoto H, editors. Comprehensive asymmetric catalysis, vol. 3. Berlin: Springer; 1999. p 1105-1120.
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.3
, pp. 1105-1120
-
-
Tomioka, K.1
Nagaoka, Y.2
-
8
-
-
0000957502
-
Conjugate addition of stabilized carbanions
-
Jacobsen EN, Pfaltz A, Yamamoto H, editors. Berlin: Springer
-
Yamaguchi M. Conjugate addition of stabilized carbanions. In: Jacobsen EN, Pfaltz A, Yamamoto H, editors. Comprehensive asymmetric catalysis, vol. 3. Berlin: Springer; 1999. p 1121-1139.
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.3
, pp. 1121-1139
-
-
Yamaguchi, M.1
-
9
-
-
1842580008
-
Control of asymmetry through conjugate addition reactions
-
Leonard J, Diez-Barra E, Merino S. Control of asymmetry through conjugate addition reactions. Eur J Org Chem 1998;10:2051-2061.
-
(1998)
Eur J Org Chem
, vol.10
, pp. 2051-2061
-
-
Leonard, J.1
Diez-Barra, E.2
Merino, S.3
-
10
-
-
0037174368
-
Direct generation of nucleophilic chiral palladium enolate from 1,3-dicarbonyl compounds: Catalytic enantioselective Michael reaction with enones
-
Hamashima Y, Hotta D, Sodeoka M. Direct generation of nucleophilic chiral palladium enolate from 1,3-dicarbonyl compounds: catalytic enantioselective Michael reaction with enones. J Am Chem Soc 2002;124:11240-11241.
-
(2002)
J Am Chem Soc
, vol.124
, pp. 11240-11241
-
-
Hamashima, Y.1
Hotta, D.2
Sodeoka, M.3
-
11
-
-
0035905575
-
Enantioselective construction of quaternary stereocenters
-
Christoffers J, Mann A. Enantioselective construction of quaternary stereocenters. Angew Chem Int Ed 2001;40:4591-4597.
-
(2001)
Angew Chem Int Ed
, vol.40
, pp. 4591-4597
-
-
Christoffers, J.1
Mann, A.2
-
12
-
-
0037007934
-
Novel asymmetric Michael addition of α-cyanopropionates to acrolein by the use of a bis(oxazolinyl)phenylstannane-derived rhodium(III) complex as a chiral lewis acid catalyst
-
Motoyama Y, Koga Y, Kobayashi K, Aoki K, Nishiyama H. Novel asymmetric Michael addition of α-cyanopropionates to acrolein by the use of a bis(oxazolinyl)phenylstannane-derived rhodium(III) complex as a chiral lewis acid catalyst. Eur Chem J 2002;8:2968-2975.
-
(2002)
Eur Chem J
, vol.8
, pp. 2968-2975
-
-
Motoyama, Y.1
Koga, Y.2
Kobayashi, K.3
Aoki, K.4
Nishiyama, H.5
-
13
-
-
0000396889
-
Stereochemical aspects in the asymmetric Michael addition of chiral imines to substituted electrophilic alkenes
-
Cave C, Desmael D, D'Angelo J, Riche C, Chiaroni A. Stereochemical aspects in the asymmetric Michael addition of chiral imines to substituted electrophilic alkenes. J Org Chem 1996;61:4361-4368.
-
(1996)
J Org Chem
, vol.61
, pp. 4361-4368
-
-
Cave, C.1
Desmael, D.2
D'Angelo, J.3
Riche, C.4
Chiaroni, A.5
-
14
-
-
0030781212
-
A new methodology for the stereoselective synthesis of 4-substituted butenolides: Asymmetric Michael addition reaction of 2-(trimethylsilyloxy)furans to oxazolidinone enoates
-
Kitajima H, Ito K, Katsuki T. A new methodology for the stereoselective synthesis of 4-substituted butenolides: asymmetric Michael addition reaction of 2-(trimethylsilyloxy)furans to oxazolidinone enoates. Tetrahedron 1997;53:17015-17028.
-
(1997)
Tetrahedron
, vol.53
, pp. 17015-17028
-
-
Kitajima, H.1
Ito, K.2
Katsuki, T.3
-
15
-
-
0033789684
-
Diastereoselective alkylation of acetoacetates of chiral inductors. Synthetic applications
-
(a) Gálvez N, Molins E, Moreno-Mañas M, Sebastian RM, Serra N, Trepat E, Vallribera AJ. Diastereoselective alkylation of acetoacetates of chiral inductors. Synthetic applications. J Heterocyclic Chem 2000;37:895-905.
-
(2000)
J Heterocyclic Chem
, vol.37
, pp. 895-905
-
-
Gálvez, N.1
Molins, E.2
Moreno-Mañas, M.3
Sebastian, R.M.4
Serra, N.5
Trepat, E.6
Vallribera, A.J.7
-
16
-
-
0033523087
-
Nickel (II)-catalyzed Michael additions. Formation of quaternary centers and diastereoselective addition of enantiopure N-acetoacetyl-4-benzyloxazolidin-2-one
-
(b) Clariana J, Gálvez N, Marchi C, Moreno-Mañas M, Vallribera A, Molins E. Nickel (II)-catalyzed Michael additions. Formation of quaternary centers and diastereoselective addition of enantiopure N-acetoacetyl-4-benzyloxazolidin-2-one. Tetrahedron 1999;55:7331-7344.
-
(1999)
Tetrahedron
, vol.55
, pp. 7331-7344
-
-
Clariana, J.1
Gálvez, N.2
Marchi, C.3
Moreno-Mañas, M.4
Vallribera, A.5
Molins, E.6
-
17
-
-
0037043171
-
Nickel (II)-catalyzed Michael additions. 2. Dynamic kinetic resolution in the reduction of chiral α-hydrazino-β-ketoacid derivatives
-
(c) Marchi C, Trepat E, Moreno-Mañas M, Vallribera A, Molins E. Nickel (II)-catalyzed Michael additions. 2. Dynamic kinetic resolution in the reduction of chiral α-hydrazino-β-ketoacid derivatives. Tetrahedron 2002;58:5699-5708.
-
(2002)
Tetrahedron
, vol.58
, pp. 5699-5708
-
-
Marchi, C.1
Trepat, E.2
Moreno-Mañas, M.3
Vallribera, A.4
Molins, E.5
-
20
-
-
0042616601
-
-
note
-
The compounds 1a and 1b were prepared by standard protocol as reported in Ref. 15b.
-
-
-
-
21
-
-
0037206789
-
Electrochemically initiated Michael addition of chiral acetoacetic derivatives to methyl vinyl ketone: Stereocontrolled construction of quaternary carbon centers
-
Palombi L, Spinella A, Feroci M, Orsini M, Inesi A. Electrochemically initiated Michael addition of chiral acetoacetic derivatives to methyl vinyl ketone: stereocontrolled construction of quaternary carbon centers. Tetrahedron Asymm 2002;13:2311-2316.
-
(2002)
Tetrahedron Asymm
, vol.13
, pp. 2311-2316
-
-
Palombi, L.1
Spinella, A.2
Feroci, M.3
Orsini, M.4
Inesi, A.5
-
22
-
-
33845471613
-
Asymmetric acylation reactions of chiral imide enolates. The first direct approach to the construction of chiral β-dicarbonyl synthons
-
Evans DA, Ennis MD, Le T. Asymmetric acylation reactions of chiral imide enolates. The first direct approach to the construction of chiral β-dicarbonyl synthons. J Am Chem Soc 1984;1154-1156.
-
(1984)
J Am Chem Soc
, pp. 1154-1156
-
-
Evans, D.A.1
Ennis, M.D.2
Le, T.3
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