-
1
-
-
0000487061
-
The Aldol reaction group I and group II enolates
-
Heathcock CH, Trost BM, Flemming I, editors. Oxford: Pergamon Press
-
Heathcock CH. The Aldol reaction group I and group II enolates. In: Heathcock CH, Trost BM, Flemming I, editors. Comprehensive Organic Synthesis vol. 2. Oxford: Pergamon Press; 1991. p 181.
-
(1991)
Comprehensive Organic Synthesis
, vol.2
, pp. 181
-
-
Heathcock, C.H.1
-
2
-
-
0001752812
-
Aldol-additions to α- and β-alkoxy aldehydes
-
(a) Reetz MT, Kesseler K, Jung A. Aldol-additions to α- and β-alkoxy aldehydes. Tetrahedron 1984;40:4327-4336.
-
(1984)
Tetrahedron
, vol.40
, pp. 4327-4336
-
-
Reetz, M.T.1
Kesseler, K.2
Jung, A.3
-
3
-
-
33845557437
-
Double stereodifferentiation with mutual kinetic resolution
-
(b) Heathcock CH, Pirrung MC, Lampe L, Buse CT, Young SD, Double stereodifferentiation with mutual kinetic resolution, J Org Chem 1981;46:2290-2300.
-
(1981)
J Org Chem
, vol.46
, pp. 2290-2300
-
-
Heathcock, C.H.1
Pirrung, M.C.2
Lampe, L.3
Buse, C.T.4
Young, S.D.5
-
4
-
-
0000110756
-
Steric effects, as well as -orbital energies, are important in diastereoface differentiation in additions to chiral aldehydes
-
(c) Lodge EP, Heathcock, CH. Steric effects, as well as -orbital energies, are important in diastereoface differentiation in additions to chiral aldehydes. J Am Chem Soc 1987;109:3353-3361.
-
(1987)
J Am Chem Soc
, vol.109
, pp. 3353-3361
-
-
Lodge, E.P.1
Heathcock, C.H.2
-
6
-
-
0000324950
-
Highly diastereoselective reactions of ytterbium-mediated alkynyl-lithium and alkynylmagnesium reagents with chiral 2-acyl-1,3-oxathianes: Reversal of diastereoselectivity
-
(b) Utimoto K, Nakamura A, Matsubara S. Highly diastereoselective reactions of ytterbium-mediated alkynyl-lithium and alkynylmagnesium reagents with chiral 2-acyl-1,3-oxathianes: Reversal of diastereoselectivity. J Am Chem Soc 1990;112: 8189-8190.
-
(1990)
J Am Chem Soc
, vol.112
, pp. 8189-8190
-
-
Utimoto, K.1
Nakamura, A.2
Matsubara, S.3
-
7
-
-
0001127065
-
Asymmetric reactions based on 1,3-oxathianes
-
Ko KY, Frazee WJ, Eliel EL. Asymmetric reactions based on 1,3-oxathianes. Tetrahedron 1984;40:1333-1343
-
(1984)
Tetrahedron
, vol.40
, pp. 1333-1343
-
-
Ko, K.Y.1
Frazee, W.J.2
Eliel, E.L.3
-
9
-
-
33847086035
-
Mild preparation of samarium iodide and ytterbium iodide and their use as reducing or coupling agents
-
(a) Girard P, Namy JL, Kagan H, Mild preparation of samarium iodide and ytterbium iodide and their use as reducing or coupling agents. J Am Chem Soc 1980; 102:2693,
-
(1980)
J Am Chem Soc
, vol.102
, pp. 2693
-
-
Girard, P.1
Namy, J.L.2
Kagan, H.3
-
10
-
-
0002774789
-
Divalent lanthanides
-
London: Academic Press
-
(b) Imamoto T. Divalent lanthanides. In: Lanthanides in Organic Synthesis. London: Academic Press; 1994. p 21.
-
(1994)
Lanthanides in Organic Synthesis
, pp. 21
-
-
Imamoto, T.1
-
11
-
-
0027539960
-
Divalent lanthanides in organic chemistry
-
(a) Kagan HB, Collin J, Namy JL, Bied C, Dallemer F, Lebrun A. Divalent lanthanides in organic chemistry, J Alloys Comp 1993;192: 191-196.
-
(1993)
J Alloys Comp
, vol.192
, pp. 191-196
-
-
Kagan, H.B.1
Collin, J.2
Namy, J.L.3
Bied, C.4
Dallemer, F.5
Lebrun, A.6
-
12
-
-
84989528750
-
Organosamariums from reaction of alkyl halides with samarium(II) derivatives
-
(b) Namy JL, Collin J, Bied C, Kagan HB. Organosamariums from reaction of alkyl halides with samarium(II) derivatives, Synlett 1992;733-734.
-
(1992)
Synlett
, pp. 733-734
-
-
Namy, J.L.1
Collin, J.2
Bied, C.3
Kagan, H.B.4
-
13
-
-
0001938996
-
A mild and convenient method for the reduction of organic halides by using a samarium diiodide-THF solution in the presence of hexamethylphosphoric triamide
-
(c) Inanaga J, Ishikawa M, Yamaguchi M. A mild and convenient method for the reduction of organic halides by using a samarium diiodide-THF solution in the presence of hexamethylphosphoric triamide. Chem Lett 1987;1485-1486.
-
(1987)
Chem Lett
, pp. 1485-1486
-
-
Inanaga, J.1
Ishikawa, M.2
Yamaguchi, M.3
-
14
-
-
85022594998
-
New mechanistic insights into reductions of halides and radicals with samarium(II) iodide
-
(d) Curran DP, Fevig TL, Jasperse CP, Totleben MJ. New mechanistic insights into reductions of halides and radicals with samarium(II) iodide. Synlett 1992; 943-961.
-
(1992)
Synlett
, pp. 943-961
-
-
Curran, D.P.1
Fevig, T.L.2
Jasperse, C.P.3
Totleben, M.J.4
-
15
-
-
26844562600
-
Stereoselective reaction with configurationally stable [α-(phenylthio)alkyl] samarium compounds
-
(e) Kasuga Y, Matsubara S, Utimoto K. Stereoselective reaction with configurationally stable [α-(phenylthio)alkyl] samarium compounds. Synlett 1998; 841-842.
-
(1998)
Synlett
, pp. 841-842
-
-
Kasuga, Y.1
Matsubara, S.2
Utimoto, K.3
-
16
-
-
0002786284
-
Ethyl γ-diiodosamario-β-oxobutanoates, generation by reaction of ethyl bromoacetate with samarium diiodide and synthetic applications
-
(f) Utimoto K, Takai T, Matsui T, Matsubara S. Ethyl γ-diiodosamario-β-oxobutanoates, generation by reaction of ethyl bromoacetate with samarium diiodide and synthetic applications. Bull Soc Chim Fr 1997;134:365-369.
-
(1997)
Bull Soc Chim Fr
, vol.134
, pp. 365-369
-
-
Utimoto, K.1
Takai, T.2
Matsui, T.3
Matsubara, S.4
-
17
-
-
29244476757
-
Highly functionalized C4 chiral synthons via Lewis acid-catalysed ene reaction to (1S)-β-pinene and α-keto ester
-
Palmino G, Dosi I, Monti D, Pellegata R. Highly functionalized C4 chiral synthons via Lewis acid-catalysed ene reaction to (1S)-β-pinene and α-keto ester. J Chem Soc Perkin Trans 1 1990;1875.
-
(1990)
J Chem Soc Perkin Trans 1
, pp. 1875
-
-
Palmino, G.1
Dosi, I.2
Monti, D.3
Pellegata, R.4
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