-
1
-
-
37049084246
-
Knoevenagel reactions with β-oxo acids. Regiospecific enol equivalents for syntheses of α,β-unsaturated ketones and of some β-ketols
-
Grayson D H, Tuite M R J. Knoevenagel reactions with β-oxo acids. Regiospecific enol equivalents for syntheses of α,β-unsaturated ketones and of some β-ketols. J Chem Soc, Perkin Trans 1, 1986, 2137-2142.
-
(1986)
J Chem Soc, Perkin Trans
, vol.1
, pp. 2137-2142
-
-
Grayson, D.H.1
Tuite, M.R.J.2
-
2
-
-
0037189273
-
A new protocol for a regioselective aldol condensation as an alternative convenient synthesis of β-ketols and α,β-unsaturated ketones
-
Kourouli T, Kefalas P, Ragoussis N, et al. A new protocol for a regioselective aldol condensation as an alternative convenient synthesis of β-ketols and α,β-unsaturated ketones. J Org Chem, 2002, 67: 4615-4618.
-
(2002)
J Org Chem
, vol.67
, pp. 4615-4618
-
-
Kourouli, T.1
Kefalas, P.2
Ragoussis, N.3
-
3
-
-
0002071853
-
Die aldolkondensation zwischen aldehyden und β-ketosäuren und ihre bedeutung für die biogenese einiger naturstoffe
-
Schöpf C, Thierfelder K. Die aldolkondensation zwischen aldehyden und β-ketosäuren und ihre bedeutung für die biogenese einiger naturstoffe. Justus Liebigs Ann Chem, 1935, 518: 127-155.
-
(1935)
Justus Liebigs Ann Chem
, vol.518
, pp. 127-155
-
-
Schöpf, C.1
Thierfelder, K.2
-
4
-
-
33750940316
-
Catalyst selectivity in the reactions of unsymmetrical ketones; Reaction of butanone with benzaldehyde and p-nitrobenzaldehyde
-
Stiles M, Wolf D, Hudson G V. Catalyst selectivity in the reactions of unsymmetrical ketones; Reaction of butanone with benzaldehyde and p-nitrobenzaldehyde. J Am Chem Soc, 1959, 81: 628-632.
-
(1959)
J Am Chem Soc
, vol.81
, pp. 628-632
-
-
Stiles, M.1
Wolf, D.2
Hudson, G.V.3
-
5
-
-
79953186649
-
Stereoselective direct amine-catalyzed decarboxylative aldol addition
-
Rohr K, Mahrwald R. Stereoselective direct amine-catalyzed decarboxylative aldol addition. Org Lett, 2011, 13: 1878-1880.
-
(2011)
Org Lett
, vol.13
, pp. 1878-1880
-
-
Rohr, K.1
Mahrwald, R.2
-
6
-
-
0041999503
-
Stabilisation of 3, 4-dihydro-2H-pyrrole (1-pyrroline) by complexation with zinc iodide
-
Baxter G, Melville J, Robins D J. Stabilisation of 3, 4-dihydro-2H-pyrrole (1-pyrroline) by complexation with zinc iodide. Synlett, 1991, 359-360.
-
(1991)
Synlett
, pp. 359-360
-
-
Baxter, G.1
Melville, J.2
Robins, D.J.3
-
7
-
-
34447318611
-
Synthesis, in vitro and in vivo cytotoxicity of 6,7-diaryl-2,3,8,8a-tetrahydroindolizin-5(1H)-ones
-
Kimball F S, Tunoori A R, Victory S F, et al. Synthesis, in vitro and in vivo cytotoxicity of 6, 7-diaryl-2, 3, 8, 8a-tetrahydroindolizin-5(1H)-ones. Bioorg Med Chem Lett, 2007, 17: 4703-4707.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 4703-4707
-
-
Kimball, F.S.1
Tunoori, A.R.2
Victory, S.F.3
-
8
-
-
0016232003
-
Decarboxylation reactions. Reaction of conjugated unsaturated ketones and nitriles with carboxylic acids
-
Fujii M, Terao Y, Sekiya M. Decarboxylation reactions. Reaction of conjugated unsaturated ketones and nitriles with carboxylic acids. Chem Pharm Bull, 1974, 22: 2675-2679.
-
(1974)
Chem Pharm Bull
, vol.22
, pp. 2675-2679
-
-
Fujii, M.1
Terao, Y.2
Sekiya, M.3
-
9
-
-
84862511337
-
A novel decarboxylative condensation of β-keto acids with 2-cyclohexen-1-one
-
Yasuda M. A novel decarboxylative condensation of β-keto acids with 2-cyclohexen-1-one. Chem Lett, 1975, 89-90.
-
(1975)
Chem Lett
, pp. 89-90
-
-
Yasuda, M.1
-
10
-
-
35048868490
-
Scope and mechanism of enantioselective Michael additions of 1,3-dicarbonyl compounds to nitroalkenes catalyzed by nickel(II)-diamine complexes
-
Evans D A, Mito S, Seidel D. Scope and mechanism of enantioselective Michael additions of 1, 3-dicarbonyl compounds to nitroalkenes catalyzed by nickel(II)-diamine complexes. J Am Chem Soc, 2007, 129: 11583-11592.
-
(2007)
J Am Chem Soc
, vol.129
, pp. 11583-11592
-
-
Evans, D.A.1
Mito, S.2
Seidel, D.3
-
11
-
-
33845374102
-
Palladium-catalyzed decarboxylative allylic alkylation of allylic acetates with β-keto acids
-
Tsuda T, Okada M, Nishi S, et al. Palladium-catalyzed decarboxylative allylic alkylation of allylic acetates with β-keto acids. J Org Chem, 1986, 51: 421-426.
-
(1986)
J Org Chem
, vol.51
, pp. 421-426
-
-
Tsuda, T.1
Okada, M.2
Nishi, S.3
-
12
-
-
0000530383
-
Palladium-catalyzed reaction of 1,3-diene monoepoxides with β-keto acids. Allylic alkylation and isomerization of 1,3-diene monoepoxides
-
Tsuda T, Tokai M, Ishida T, et al. Palladium-catalyzed reaction of 1, 3-diene monoepoxides with β-keto acids. Allylic alkylation and isomerization of 1, 3-diene monoepoxides. J Org Chem, 1986, 51: 5216-5221.
-
(1986)
J Org Chem
, vol.51
, pp. 5216-5221
-
-
Tsuda, T.1
Tokai, M.2
Ishida, T.3
-
13
-
-
79960394242
-
Catalytic decarboxylative alkylation of β-keto acids with sulfonamides via the cleavage of carbon-nitrogen and carbon-carbon bonds
-
Yang C F, Wang J Y, Tian S K. Catalytic decarboxylative alkylation of β-keto acids with sulfonamides via the cleavage of carbon-nitrogen and carbon-carbon bonds. Chem Commun, 2011, 47: 8343-8345.
-
(2011)
Chem Commun
, vol.47
, pp. 8343-8345
-
-
Yang, C.F.1
Wang, J.Y.2
Tian, S.K.3
-
14
-
-
58449134253
-
Selective benzylic and allylic alkylation of protic nucleophiles with sulfonamides through double lewis acid catalyzed cleavage of sp3 carbon-nitrogen bonds
-
Liu C R, Li M B, Yang C F, et al. Selective benzylic and allylic alkylation of protic nucleophiles with sulfonamides through double lewis acid catalyzed cleavage of sp3 carbon-nitrogen bonds. Chem Eur J, 2009, 15: 793-797.
-
(2009)
Chem Eur J
, vol.15
, pp. 793-797
-
-
Liu, C.R.1
Li, M.B.2
Yang, C.F.3
-
15
-
-
67149097945
-
3 C-N bond cleavage at room temperature
-
3 C-N bond cleavage at room temperature. Org Lett, 2009, 11: 2543-2545.
-
(2009)
Org Lett
, vol.11
, pp. 2543-2545
-
-
Liu, C.R.1
Li, M.B.2
Cheng, D.J.3
-
16
-
-
77956205958
-
Catalytic regioselective synthesis of structurally diverse indene derivatives from N-benzylic sulfonamides and disubstituted alkynes
-
Liu C R, Yang F L, Jin Y Z, et al. Catalytic regioselective synthesis of structurally diverse indene derivatives from N-benzylic sulfonamides and disubstituted alkynes. Org Lett, 2010, 12: 3832-3835.
-
(2010)
Org Lett
, vol.12
, pp. 3832-3835
-
-
Liu, C.R.1
Yang, F.L.2
Jin, Y.Z.3
-
17
-
-
77955785933
-
Catalytic coupling of N-benzylic sulfonamides with silylated nucleophiles at room temperature
-
Yang B L, Tian S K. Catalytic coupling of N-benzylic sulfonamides with silylated nucleophiles at room temperature. Chem Commun, 2010, 46: 6180-6182.
-
(2010)
Chem Commun
, vol.46
, pp. 6180-6182
-
-
Yang, B.L.1
Tian, S.K.2
-
19
-
-
80054098215
-
Catalytic asymmetric α-alkylation of ketones and aldehydes with N-benzylic sulfonamides through carbon-nitrogen bond cleavage
-
Weng Z T, Li Y, Tian S K. Catalytic asymmetric α-alkylation of ketones and aldehydes with N-benzylic sulfonamides through carbon-nitrogen bond cleavage. J Org Chem, 2011, 76: 8095-8099.
-
(2011)
J Org Chem
, vol.76
, pp. 8095-8099
-
-
Weng, Z.T.1
Li, Y.2
Tian, S.K.3
-
20
-
-
84055191469
-
Catalytic asymmetric cleavage of sp3 C-N bonds for access to highly enantioenriched N-benzylic sulfonamides
-
Wu X S, Tian S K. Catalytic asymmetric cleavage of sp3 C-N bonds for access to highly enantioenriched N-benzylic sulfonamides. Chem Commun, 2012, 48: 898-900.
-
(2012)
Chem Commun
, vol.48
, pp. 898-900
-
-
Wu, X.S.1
Tian, S.K.2
-
22
-
-
70349845760
-
Iron(III) chloride-catalysed direct nucleophilic α-substitution of Morita-Baylis-Hillman alcohols with alcohols, arenes, 1,3-dicarbonyl compounds, and thiols
-
Zhang X, Rao W, Chan P W H. Iron(III) chloride-catalysed direct nucleophilic α-substitution of Morita-Baylis-Hillman alcohols with alcohols, arenes, 1, 3-dicarbonyl compounds, and thiols. Org Biomol Chem, 2009, 7: 4186-4193.
-
(2009)
Org Biomol Chem
, vol.7
, pp. 4186-4193
-
-
Zhang, X.1
Rao, W.2
Chan, P.W.H.3
-
24
-
-
22244490027
-
Substitution of benzylic hydroxyl groups with vinyl moieties using vinylboron dihalides
-
Kabalka W G, Yao M L, Borella S, et al. Substitution of benzylic hydroxyl groups with vinyl moieties using vinylboron dihalides. Org Lett, 2005, 7: 2865-2867.
-
(2005)
Org Lett
, vol.7
, pp. 2865-2867
-
-
Kabalka, W.G.1
Yao, M.L.2
Borella, S.3
-
25
-
-
33846451020
-
Bismuth-catalyzed direct substitution of the hydroxy group in alcohols with sulfonamides, carbamates, and carboxamides
-
Qin H, Yamagiwa N, Matsunaga S, et al. Bismuth-catalyzed direct substitution of the hydroxy group in alcohols with sulfonamides, carbamates, and carboxamides. Angew Chem Int Ed, 2007, 46: 409-413.
-
(2007)
Angew Chem Int Ed
, vol.46
, pp. 409-413
-
-
Qin, H.1
Yamagiwa, N.2
Matsunaga, S.3
-
26
-
-
53749093735
-
Three-component synthesis of amine derivatives using benzylic and allylic alcohols as N-alkylating agents in the absence of external catalysts and additives
-
Li H H, Dong D J, Tian S K. Three-component synthesis of amine derivatives using benzylic and allylic alcohols as N-alkylating agents in the absence of external catalysts and additives. Eur J Org Chem, 2008, 3623-3626.
-
(2008)
Eur J Org Chem
, pp. 3623-3626
-
-
Li, H.H.1
Dong, D.J.2
Tian, S.K.3
-
27
-
-
68149100771
-
Controllable stereoselective synthesis of trisubstituted alkenes by a catalytic three-component reaction of terminal alkynes, benzylic alcohols, and simple arenes
-
Li H H, Jin Y H, Wang J Q, et al. Controllable stereoselective synthesis of trisubstituted alkenes by a catalytic three-component reaction of terminal alkynes, benzylic alcohols, and simple arenes. Org Bio Chem, 2009, 7: 3219-3221.
-
(2009)
Org Bio Chem
, vol.7
, pp. 3219-3221
-
-
Li, H.H.1
Jin, Y.H.2
Wang, J.Q.3
-
28
-
-
73149122781
-
An expeditious entry to benzylic and allylic sulfones through byproduct-catalyzed reaction of alcohols with sulfinyl chlorides
-
Li H H, Dong D J, Jin Y H, et al. An expeditious entry to benzylic and allylic sulfones through byproduct-catalyzed reaction of alcohols with sulfinyl chlorides. J Org Chem, 2009, 74: 9501-9504.
-
(2009)
J Org Chem
, vol.74
, pp. 9501-9504
-
-
Li, H.H.1
Dong, D.J.2
Jin, Y.H.3
-
30
-
-
11144323895
-
Iron-catalyzed reactions in organic synthesis
-
Bolm C, Legros J, Le Paih J, et al. Iron-catalyzed reactions in organic synthesis. Chem Rev, 2004, 104: 6217-6254.
-
(2004)
Chem Rev
, vol.104
, pp. 6217-6254
-
-
Bolm, C.1
Legros, J.2
Le Paih, J.3
-
31
-
-
56749104228
-
Iron(III)-catalyzed addition of benzylic alcohols to aryl alkynes-A new synthesis of substituted aryl ketones
-
Jana U, Biswas S, Maiti S. Iron(III)-catalyzed addition of benzylic alcohols to aryl alkynes-A new synthesis of substituted aryl ketones. Eur J Org Chem, 2008, 5798-5804.
-
(2008)
Eur J Org Chem
, pp. 5798-5804
-
-
Jana, U.1
Biswas, S.2
Maiti, S.3
-
32
-
-
57649159510
-
3-catalyzed propargylation-cycloisomerization tandem reaction: A facile one-pot synthesis of substituted furans
-
3-catalyzed propargylation-cycloisomerization tandem reaction: A facile one-pot synthesis of substituted furans. Synlett, 2008, 3046-3052.
-
(2008)
Synlett
, pp. 3046-3052
-
-
Ji, W.H.1
Pan, Y.M.2
Zhao, S.Y.3
-
34
-
-
67650022790
-
2O-catalyzed intramolecular Friedel-Crafts reaction of aryl-substituted allylic alcohols
-
2O-catalyzed intramolecular Friedel-Crafts reaction of aryl-substituted allylic alcohols. Tetrahedron Lett, 2009, 50: 4978-4982.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 4978-4982
-
-
Wang, J.1
Zhang, L.2
Jing, Y.3
-
35
-
-
31444456960
-
Direct carbon-carbon bond formation from alcohols and active methylenes, alkoxyketones, or indoles catalyzed by indium trichloride
-
Yasuda M, Somyo T, Baba A. Direct carbon-carbon bond formation from alcohols and active methylenes, alkoxyketones, or indoles catalyzed by indium trichloride. Angew Chem Int Ed, 2006, 45: 793-796.
-
(2006)
Angew Chem Int Ed
, vol.45
, pp. 793-796
-
-
Yasuda, M.1
Somyo, T.2
Baba, A.3
-
36
-
-
37649003787
-
3-catalyzed amidation reaction of secondary benzylic and allylic alcohols with carboxamides or p-toluenesulfonamide
-
3-catalyzed amidation reaction of secondary benzylic and allylic alcohols with carboxamides or p-toluenesulfonamide. Tetrahedron Lett, 2008, 49: 858-862.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 858-862
-
-
Jana, U.1
Maiti, S.2
Biswas, S.3
|