-
1
-
-
0027465609
-
First general synthesis of monosilyl acetals. Trimethylsilyl trapping of the intermediate in DIBALH reduction of carboxylic acid esters using trimethylsilyl trifluoromethanesulfonate
-
(a) Kiyooka S, Shirouchi M, Kaneko Y. First general synthesis of monosilyl acetals. Trimethylsilyl trapping of the intermediate in DIBALH reduction of carboxylic acid esters using trimethylsilyl trifluoromethanesulfonate. Tetrahedron Lett 1993;34:1491-1494.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 1491-1494
-
-
Kiyooka, S.1
Shirouchi, M.2
Kaneko, Y.3
-
2
-
-
0001268766
-
General synthesis of α-acetoxy ethers from esters by DIBALH reduction and acetylation
-
(b) Dahanukar VH, Rychnovsky SD. General synthesis of α-acetoxy ethers from esters by DIBALH reduction and acetylation. J Org Chem 1996; 61:8317-8320,
-
(1996)
J Org Chem
, vol.61
, pp. 8317-8320
-
-
Dahanukar, V.H.1
Rychnovsky, S.D.2
-
3
-
-
33845375690
-
Acylation of organolithium reagents by esters in the presence of chlorotrimethylsilane
-
(c) Cooke MP Jr. Acylation of organolithium reagents by esters in the presence of chlorotrimethylsilane. J Org Chem 1986; 51:951-953.
-
(1986)
J Org Chem
, vol.51
, pp. 951-953
-
-
Cooke M.P., Jr.1
-
4
-
-
0010247489
-
Preparation of alkyl silyl acetals from carboxylic esters with tert-butyldimethylsilyldihalomethyllithium. 1,3-Rearrangement of silyl group from carbon to oxide
-
Shinokubo H, Oshima K, Utimoto K. Preparation of alkyl silyl acetals from carboxylic esters with tert-butyldimethylsilyldihalomethyllithium. 1,3-Rearrangement of silyl group from carbon to oxide. Chem Lett 1995;461-462.
-
(1995)
Chem Lett
, pp. 461-462
-
-
Shinokubo, H.1
Oshima, K.2
Utimoto, K.3
-
7
-
-
0002633617
-
A simple preparation of trimethylsilylacetonitrile and a novel ring-opening of epoxides with trimethylsilylacetonitrile anion
-
(a) Matsuda I, Murata S, Ishii Y. A simple preparation of trimethylsilylacetonitrile and a novel ring-opening of epoxides with trimethylsilylacetonitrile anion. J Chem Soc Perkin Trans 1 1979:26-30.
-
(1979)
J Chem Soc Perkin Trans 1
, pp. 26-30
-
-
Matsuda, I.1
Murata, S.2
Ishii, Y.3
-
8
-
-
0001261296
-
A simple synthesis of α-ylidene γ-lactones from γ-trimethylsiloxy nitriles
-
(b) Matsuda I, Murata S, Izumi Y. A simple synthesis of α-ylidene γ-lactones from γ-trimethylsiloxy nitriles. Bull Chem Soc Jpn 1979;52:2389-2393.
-
(1979)
Bull Chem Soc Jpn
, vol.52
, pp. 2389-2393
-
-
Matsuda, I.1
Murata, S.2
Izumi, Y.3
-
9
-
-
0001441950
-
N-substituted organo(silyliminomethyl)stannanes: Synthetic equivalent to organosilylcarbonyl anion and carbonyl dianion
-
(c) Ito Y, Matsuura T, Murakami M. N-substituted organo(silyliminomethyl)stannanes: Synthetic equivalent to organosilylcarbonyl anion and carbonyl dianion. J Am Chem Soc 1987;109:7888-7890.
-
(1987)
J Am Chem Soc
, vol.109
, pp. 7888-7890
-
-
Ito, Y.1
Matsuura, T.2
Murakami, M.3
-
10
-
-
0344070356
-
Reaction of β-heteroatom-substituted α,β-unsaturated acylsilanes with ketone enolates: A new [3 + 2] annulation based on Brook rearrangement
-
(d) Takeda K, Fujisawa M, Makino T, Yoshii E. Reaction of β-heteroatom-substituted α,β-unsaturated acylsilanes with ketone enolates: A new [3 + 2] annulation based on Brook rearrangement. J Am Chem Soc 1993; 115:9351-9352.
-
(1993)
J Am Chem Soc
, vol.115
, pp. 9351-9352
-
-
Takeda, K.1
Fujisawa, M.2
Makino, T.3
Yoshii, E.4
-
12
-
-
84988058001
-
2-symmetrical enantiopure 1,5-diols and β,β′-dihydroxyketones as well as of enantiopure 1,3,5-triols
-
2-symmetrical enantiopure 1,5-diols and β,β′-dihydroxyketones as well as of enantiopure 1,3,5-triols. Synlett 1994:511-512.
-
(1994)
Synlett
, pp. 511-512
-
-
Tietze, L.F.1
Geissler, H.2
Gewert, J.A.3
Jacobi, U.4
-
13
-
-
0001006337
-
New [3 + 4] annulation. Reactions of (β-(trimethylsilyl)acryloyl)silanes with the lithium enolates of α,β-unsaturated methyl ketones
-
(g) Takeda K, Takeda M, Nakajima A, Yoshii E. New [3 + 4] annulation. Reactions of (β-(trimethylsilyl)acryloyl)silanes with the lithium enolates of α,β-unsaturated methyl ketones. J Am Chem Soc 1995;117:6400-6401.
-
(1995)
J Am Chem Soc
, vol.117
, pp. 6400-6401
-
-
Takeda, K.1
Takeda, M.2
Nakajima, A.3
Yoshii, E.4
-
14
-
-
0030812082
-
Multicomponent linchpin couplings of silyl dithianes via solvent-controlled Brook rearrangement
-
(h) Smith AB III, Boldi AM. Multicomponent linchpin couplings of silyl dithianes via solvent-controlled Brook rearrangement. J Am Chem Soc 1997;119:6925-6926.
-
(1997)
J Am Chem Soc
, vol.119
, pp. 6925-6926
-
-
Smith A.B. III1
Boldi, A.M.2
-
15
-
-
0032560046
-
Sequential carbon-carbon bond formation reaction using 1-silyl-2-propenyllithium
-
(i) Takaku K, Shinokubo H, Oshima K. Sequential carbon-carbon bond formation reaction using 1-silyl-2-propenyllithium. Tetrahedron Lett 1998;39:2575-2578.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2575-2578
-
-
Takaku, K.1
Shinokubo, H.2
Oshima, K.3
-
16
-
-
0025095596
-
1,2-Addition of dimethyl(phenyl)silyllithium to cyclic α,β-unsaturated ketones and regiospecific generation of cyclic silyl enol ethers through Brook rearrangement of 1,2-addition products
-
(j) Koreeda M, Koo S. 1,2-Addition of dimethyl(phenyl)silyllithium to cyclic α,β-unsaturated ketones and regiospecific generation of cyclic silyl enol ethers through Brook rearrangement of 1,2-addition products. Tetrahedron Lett 1990;31:831-834.
-
(1990)
Tetrahedron Lett
, vol.31
, pp. 831-834
-
-
Koreeda, M.1
Koo, S.2
-
17
-
-
0002688377
-
Tandem transformations initiated by the migration of a silyl group. Some new synthetic applications of silyloxiranes
-
Jankowski P, Raubo P, Wicha J. Tandem transformations initiated by the migration of a silyl group. Some new synthetic applications of silyloxiranes. Synlett 1994:985-992.
-
(1994)
Synlett
, pp. 985-992
-
-
Jankowski, P.1
Raubo, P.2
Wicha, J.3
-
18
-
-
0027471608
-
tert-butyldimethylsilyldihalomethyllithium as a dihalomethylene dianion synthon. 1,3-Rearrangement of silyl group from carbon to oxide
-
(a) Shinokubo H, Miura K, Oshima K, Utimoto K. tert-butyldimethylsilyldihalomethyllithium as a dihalomethylene dianion synthon. 1,3-Rearrangement of silyl group from carbon to oxide. Tetrahedron Lett 1993;34:1951-1954.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 1951-1954
-
-
Shinokubo, H.1
Miura, K.2
Oshima, K.3
Utimoto, K.4
-
19
-
-
0030030939
-
tert-butyldimethylsilyldihalomethyllithium as a dihalomethylene dianion synthon. 1,3-Rearrangement and 1,4-rearrangement of silyl group from carbon to oxide
-
(b) Shinokubo H, Miura K, Oshima K, Utimoto K. tert-butyldimethylsilyldihalomethyllithium as a dihalomethylene dianion synthon. 1,3-Rearrangement and 1,4-rearrangement of silyl group from carbon to oxide. Tetrahedron 1996;52:503-514.
-
(1996)
Tetrahedron
, vol.52
, pp. 503-514
-
-
Shinokubo, H.1
Miura, K.2
Oshima, K.3
Utimoto, K.4
-
20
-
-
0000407979
-
Enantioselective chiral borane-mediated aldol reactions of silyl ketene acetals with aldehydes. Novel effect of the trialkylsilyl group of the silyl ketene acetal on the reaction course
-
(a) Kiyooka S, Kaneko Y, Matsuo H, Nakano M. Enantioselective chiral borane-mediated aldol reactions of silyl ketene acetals with aldehydes. Novel effect of the trialkylsilyl group of the silyl ketene acetal on the reaction course. J Org Chem 1991;56:2276-2278.
-
(1991)
J Org Chem
, vol.56
, pp. 2276-2278
-
-
Kiyooka, S.1
Kaneko, Y.2
Matsuo, H.3
Nakano, M.4
-
21
-
-
0001631795
-
Stereoselective synthesis of allyl vinyl ethers from silyl enol ethers
-
(b) Maeda K, Shinokubo H, Oshima K, Utimoto K. Stereoselective synthesis of allyl vinyl ethers from silyl enol ethers. J Org Chem 1996;61:2262-2263.
-
(1996)
J Org Chem
, vol.61
, pp. 2262-2263
-
-
Maeda, K.1
Shinokubo, H.2
Oshima, K.3
Utimoto, K.4
-
22
-
-
0001569781
-
Facile preparation of vicinal allylsiloxy- and vinylsiloxyhaloalkanes and their radical cyclization reaction
-
(c) Shinokubo H, Oshima K, Utimoto K. Facile preparation of vicinal allylsiloxy- and vinylsiloxyhaloalkanes and their radical cyclization reaction. Bull Chem Soc Jpn 1997;70:2255-2263.
-
(1997)
Bull Chem Soc Jpn
, vol.70
, pp. 2255-2263
-
-
Shinokubo, H.1
Oshima, K.2
Utimoto, K.3
-
23
-
-
0000778448
-
Lewis acid-induced chemo- and stereoselective allylation of β-iodo mixed acetal with allylsilane
-
(d) Maeda K, Shinokubo H, Oshima K. Lewis acid-induced chemo- and stereoselective allylation of β-iodo mixed acetal with allylsilane. J Org Chem 1997;62:6429-6429.
-
(1997)
J Org Chem
, vol.62
, pp. 6429
-
-
Maeda, K.1
Shinokubo, H.2
Oshima, K.3
-
24
-
-
0028361224
-
One-pot synthesis of α,β-unsaturated ketones from tert-butyldimethylsilyldibromomethane and two different aldehydes
-
(a) Shinokubo H, Oshima K, Utimoto K. One-pot synthesis of α,β-unsaturated ketones from tert-butyldimethylsilyldibromomethane and two different aldehydes. Tetrahedron Lett 1994;35:3741-3744.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 3741-3744
-
-
Shinokubo, H.1
Oshima, K.2
Utimoto, K.3
-
25
-
-
0030580396
-
Facile syntheses of α-bromo-α-silyl ketones and α-bromoacylsilanes from tert-butyldimethylsilyldibromomethane and carbonyl compounds
-
(b) Shinokubo H, Oshima K, Utimoto K. Facile syntheses of α-bromo-α-silyl ketones and α-bromoacylsilanes from tert-butyldimethylsilyldibromomethane and carbonyl compounds. Tetrahedron 1996;54:14533-14542.
-
(1996)
Tetrahedron
, vol.54
, pp. 14533-14542
-
-
Shinokubo, H.1
Oshima, K.2
Utimoto, K.3
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