-
1
-
-
33645381883
-
Ueber einen Aldehyd-Alkohol.
-
Wurtz, A. Ueber einen Aldehyd-Alkohol. J. Prakt. Chemie, 1872, 5(1), 457-464.
-
(1872)
J. Prakt. Chemie
, vol.5
, Issue.1
, pp. 457-464
-
-
Wurtz, A.1
-
2
-
-
33846463792
-
Highly selective acetate aldol additions using mesityl-substituted chiral auxiliaries
-
Crimmins, M. T.; Shamszad, M. Highly selective acetate aldol additions using mesityl-substituted chiral auxiliaries. Org. Lett. 2007, 9, 149-152.
-
(2007)
Org. Lett
, vol.9
, pp. 149-152
-
-
Crimmins, M.T.1
Shamszad, M.2
-
3
-
-
35348861428
-
Enantioselective direct aldol reaction: The blossoming of modern organocatalysis
-
Guillena, G.; Nájera, C.; Ramón, D. J. Enantioselective direct aldol reaction: the blossoming of modern organocatalysis. Tetrahedron: Asymmetry 2007, 2249-2293.
-
(2007)
Tetrahedron: Asymmetry
, pp. 2249-2293
-
-
Guillena, G.1
Nájera, C.2
Ramón, D.J.3
-
4
-
-
33845219123
-
Modern aldol methods for the total synthesis of polyketides
-
Mahrwald, R.; Schetter, B. Modern aldol methods for the total synthesis of polyketides. Angew. Chem. 2006, 45, 7506-7525.
-
(2006)
Angew. Chem
, vol.45
, pp. 7506-7525
-
-
Mahrwald, R.1
Schetter, B.2
-
5
-
-
34547130040
-
Lewis base activation of lewis acids: Catalytic, enantioselective with high regio- and stereoselectivity
-
For Lewis base activation of Lewis acids, see
-
For Lewis base activation of Lewis acids, see Denmark, S. E.; Heemstra, J. R. Lewis base activation of lewis acids: Catalytic, enantioselective with high regio- and stereoselectivity. J. Org. Chem. 2007, 72, 5668-5688.
-
(2007)
J. Org. Chem
, vol.72
, pp. 5668-5688
-
-
Denmark, S.E.1
Heemstra, J.R.2
-
6
-
-
34250189569
-
Small organic molecule in enatioselective, direct aldol reaction in Water
-
Aratake, S.; Itoh, T.; Okano, T.; Usui, T.; Shoji, M.; Hayashi, Y. Small organic molecule in enatioselective, direct aldol reaction "in Water." Chem Comm. 2007, 2524-2426.
-
(2007)
Chem Comm
, pp. 2524-2426
-
-
Aratake, S.1
Itoh, T.2
Okano, T.3
Usui, T.4
Shoji, M.5
Hayashi, Y.6
-
7
-
-
34547144181
-
Highly Enantioselective Organocatalytic direct aldol reaction in an aqueous medium
-
Maya, V.; Raj, M.; Singh, V. K. Highly Enantioselective Organocatalytic direct aldol reaction in an aqueous medium. Org Lett. 2007, 9, 2593-2595.
-
(2007)
Org Lett
, vol.9
, pp. 2593-2595
-
-
Maya, V.1
Raj, M.2
Singh, V.K.3
-
8
-
-
0012016624
-
Enantioselective aldol condensations 2. erythro-selective chiral aldol condensations via boron enolates
-
Evans, D. A.; Bartroli, J.; Shih, T. L. Enantioselective aldol condensations 2. erythro-selective chiral aldol condensations via boron enolates. J. Am. Chem. Soc. 1981, 103, 2127-2129.
-
(1981)
J. Am. Chem. Soc
, vol.103
, pp. 2127-2129
-
-
Evans, D.A.1
Bartroli, J.2
Shih, T.L.3
-
9
-
-
0035830561
-
Asymmetric aldol additions: Use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones
-
Crimmins, M. T.; King, B. W.; Tabet, E. A.; Chaudhary, K. Asymmetric aldol additions: use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones. J. Org. Chem. 2001, 66, 894-902.
-
(2001)
J. Org. Chem
, vol.66
, pp. 894-902
-
-
Crimmins, M.T.1
King, B.W.2
Tabet, E.A.3
Chaudhary, K.4
-
10
-
-
0033955174
-
Steroselectivity in aldol reactions of chiral N-acyl selones
-
Li, Z.; Wu, R.; Michalczyk, R.; Dunlap, R. B.; Odom, J. D.; Silks, L. A. P. Steroselectivity in aldol reactions of chiral N-acyl selones. J. Am. Chem. Soc. 2000, 122, 386-387.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 386-387
-
-
Li, Z.1
Wu, R.2
Michalczyk, R.3
Dunlap, R.B.4
Odom, J.D.5
Silks, L.A.P.6
-
11
-
-
0037669293
-
Anti-selective aldol reactions with titanium enolates of N-glycolyloxazolidinethiones
-
Also see
-
Also see, Crimmins, M. T.; McDougall, P. J. Anti-selective aldol reactions with titanium enolates of N-glycolyloxazolidinethiones. Org. Lett. 2003, 5, 591-594.
-
(2003)
Org. Lett
, vol.5
, pp. 591-594
-
-
Crimmins, M.T.1
McDougall, P.J.2
-
12
-
-
0034283378
-
77Se HMQC NMR spectroscopy and x-ray crystallography
-
and references therein
-
77Se HMQC NMR spectroscopy and x-ray crystallography. Angew. Chem. Int. Ed. 2000, 39, 3067-3070, and references therein.
-
(2000)
Angew. Chem. Int. Ed
, vol.39
, pp. 3067-3070
-
-
Michalczyk, R.1
Schmidt, J.G.2
Moody, E.3
Li, Z.4
Wu, R.5
Dunlap, B.6
Odom, J.D.7
Silks III, L.A.8
-
13
-
-
0344430143
-
Determining the solution state orientation of a Ti enolate via stable isotope labelling. NMR spectroscopy, and modeling studies
-
Kimball, D. B.; Michalczyk, R.; Moody, E.; Ollivault-Shiflett, M.; De Jesus, K.; Silks, L. A. III. Determining the solution state orientation of a Ti enolate via stable isotope labelling. NMR spectroscopy, and modeling studies. J. Am. Chem. Soc. 2003, 125, 14666-14667.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 14666-14667
-
-
Kimball, D.B.1
Michalczyk, R.2
Moody, E.3
Ollivault-Shiflett, M.4
De Jesus, K.5
Silks III, L.A.6
-
14
-
-
61849176987
-
-
Kimball, D. B.; Silks, L. A. P. Unpublished results; (b) Kimball, D. B.; Silks, L. A. P.; Ollivault-Shiflett, M.; Michalczyk, R.; Moody, E. Abstracts of Papers of the American Chemical Society 2003, 226, U209-U210.
-
(a) Kimball, D. B.; Silks, L. A. P. Unpublished results; (b) Kimball, D. B.; Silks, L. A. P.; Ollivault-Shiflett, M.; Michalczyk, R.; Moody, E. Abstracts of Papers of the American Chemical Society 2003, 226, U209-U210.
-
-
-
-
15
-
-
0037182708
-
Practical and highly selective oxazolidinethionebased asymmetric acetate aldol reactions with aliphatic aldehydes
-
and references therein;
-
(a) Guz, N. R.; Phillips, A. J. Practical and highly selective oxazolidinethionebased asymmetric acetate aldol reactions with aliphatic aldehydes. Org. Lett. 2002, 4, 2253-2256, and references therein;
-
(2002)
Org. Lett
, vol.4
, pp. 2253-2256
-
-
Guz, N.R.1
Phillips, A.J.2
-
16
-
-
0033521679
-
Diastereoselective aldol reaction with an acetate enolate: 2,6-bis(2-isopropylphenyl)-3,5- dimethylphenol as an extremely effective chiral auxiliary
-
and references therein;
-
(b) Saito, S.; Hatanaka, K.; Kano, T.; Yamamoto, H. Diastereoselective aldol reaction with an acetate enolate: 2,6-bis(2-isopropylphenyl)-3,5- dimethylphenol as an extremely effective chiral auxiliary. Angew. Chem. Int. Ed. 1998, 37, 3378-3381, and references therein;
-
(1998)
Angew. Chem. Int. Ed
, vol.37
, pp. 3378-3381
-
-
Saito, S.1
Hatanaka, K.2
Kano, T.3
Yamamoto, H.4
-
17
-
-
0033523219
-
Boron-mediated double aldol reaction of carboxylic esters
-
(c) Abiko, A.; Liu, J.-F.; Buske, D. C.; Moriyama, S.; Masamune, S. Boron-mediated double aldol reaction of carboxylic esters. J. Am Chem. Soc. 1999, 121, 7168-7169;
-
(1999)
J. Am Chem. Soc
, vol.121
, pp. 7168-7169
-
-
Abiko, A.1
Liu, J.-F.2
Buske, D.C.3
Moriyama, S.4
Masamune, S.5
-
18
-
-
0037064482
-
Asymmetric double aldol reaction of chiral acetyloxazolidinone
-
(d) Furuno, H.; Inoue, T.; Abiko, A. Asymmetric double aldol reaction of chiral acetyloxazolidinone. Tetrahedron Lett. 2002, 43, 8297-8299;
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 8297-8299
-
-
Furuno, H.1
Inoue, T.2
Abiko, A.3
-
19
-
-
84973329202
-
Amino acid catalyzed direct asymmetric aldol reactions: A bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions
-
(e) Braun, M. Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions. Angew. Chem., Int. Ed. Engl. 1987, 26, 24-37;
-
(1987)
Angew. Chem., Int. Ed. Engl
, vol.26
, pp. 24-37
-
-
Braun, M.1
-
20
-
-
11844259698
-
-
Mahrwald, R, Ed, Wiley-VCH: Weinheim
-
(f) Modern Aldol Reactions; Mahrwald, R., Ed.; Wiley-VCH: Weinheim, 2004; vol. 1-2;
-
(2004)
Modern Aldol Reactions
, vol.1-2
-
-
-
21
-
-
1642386775
-
Current progress in the asymmetric aldol addition reaction
-
(g) Palomo, C.; Oiarbide, M.; García, J. M. Current progress in the asymmetric aldol addition reaction. Chem. Soc. Rev. 2004, 33, 65-75;
-
(2004)
Chem. Soc. Rev
, vol.33
, pp. 65-75
-
-
Palomo, C.1
Oiarbide, M.2
García, J.M.3
-
22
-
-
0034678591
-
The Catalytic asymmetric aldol reaction
-
(h) Machajewski, T. D.; Wong, C.-H. The Catalytic asymmetric aldol reaction. Angew. Chem. Int. Ed. 2000, 39, 1352-1374;
-
(2000)
Angew. Chem. Int. Ed
, vol.39
, pp. 1352-1374
-
-
Machajewski, T.D.1
Wong, C.-H.2
-
23
-
-
33749434107
-
Current progress in the acetate/methyl ketone aldol reaction
-
(i) Kimball, D. B.; Silks, L. A. P. Current progress in the acetate/methyl ketone aldol reaction. Curr. Org. Chem. 2006, 10, 1975-1992.
-
(2006)
Curr. Org. Chem
, vol.10
, pp. 1975-1992
-
-
Kimball, D.B.1
Silks, L.A.P.2
-
24
-
-
39749135372
-
Indene-based thiazolidinethione chiral auxiliary for propionate and acetate aldol additions
-
Osorio-Lozada, A.; Olivo, H. F. Indene-based thiazolidinethione chiral auxiliary for propionate and acetate aldol additions. Org. Lett. 2008, 617-620.
-
(2008)
Org. Lett
, pp. 617-620
-
-
Osorio-Lozada, A.1
Olivo, H.F.2
-
25
-
-
0026541844
-
Highly enantioselective aldol reaction - development of a new chiral auxiliary from cis-1-amino-2- hydroxyindan
-
Ghosh, A. K.; Duong, T. T.; Mckee, S. P. Highly enantioselective aldol reaction - development of a new chiral auxiliary from cis-1-amino-2- hydroxyindan. J. Chem. Soc., Chem. Commun. 1992, 1673-1674.
-
(1992)
J. Chem. Soc., Chem. Commun
, pp. 1673-1674
-
-
Ghosh, A.K.1
Duong, T.T.2
Mckee, S.P.3
-
26
-
-
0000629154
-
Quantitative detection of remotely disposed chiral centers using Se-77 NMR spectroscopy
-
Silks, L. A.; Dunlap, R. B.; Odom, J. D. Quantitative detection of remotely disposed chiral centers using Se-77 NMR spectroscopy. J. Am Chem. Soc. 1990, 112, 4979-4982.
-
(1990)
J. Am Chem. Soc
, vol.112
, pp. 4979-4982
-
-
Silks, L.A.1
Dunlap, R.B.2
Odom, J.D.3
-
27
-
-
0001497764
-
Syntheses Via-2-oxazolines 1: Formylation of grignard reagents in presence of hexamethylphosphoramide
-
(a) Meyers, A. I.; Collington, E. W. Syntheses Via-2-oxazolines 1: Formylation of grignard reagents in presence of hexamethylphosphoramide. J. Am. Chem. Soc. 1970, 92, 6676-6678;
-
(1970)
J. Am. Chem. Soc
, vol.92
, pp. 6676-6678
-
-
Meyers, A.I.1
Collington, E.W.2
-
28
-
-
0000618195
-
A rapid and efficient synthesis of chiral 2-hydro-2-oxazolines
-
(b) Leonard, W. R.; Romine, J. L.; Meyers, A. I. A rapid and efficient synthesis of chiral 2-hydro-2-oxazolines. J. Org. Chem. 1991, 56, 1961-1963;
-
(1991)
J. Org. Chem
, vol.56
, pp. 1961-1963
-
-
Leonard, W.R.1
Romine, J.L.2
Meyers, A.I.3
-
29
-
-
0001467882
-
Synthesis and characterization of chiral oxazolidine-2-selone: A general one-step procedure from readily available oxazolines
-
(c) Peng, J.; Barr, M. E.; Ashburn, D. A.; Odom, J. D.; Dunlap, R. B.; Silks, L. A. Synthesis and characterization of chiral oxazolidine-2-selone: a general one-step procedure from readily available oxazolines. J. Org. Chem. 1994, 59, 4977-4987.
-
(1994)
J. Org. Chem
, vol.59
, pp. 4977-4987
-
-
Peng, J.1
Barr, M.E.2
Ashburn, D.A.3
Odom, J.D.4
Dunlap, R.B.5
Silks, L.A.6
-
30
-
-
33947085552
-
Nuclear magnetic-resonance enantiomer reagents - configurational correlations via nuclear magnetic-resonance chemical-shifts of diastereomeric mandelate, O-methylmandelate, and alpha-methoxy-alpha- trifluoromethylphenylacetate (MTPA) Esters
-
Dale, J. A.; Mosher, H. S. Nuclear magnetic-resonance enantiomer reagents - configurational correlations via nuclear magnetic-resonance chemical-shifts of diastereomeric mandelate, O-methylmandelate, and alpha-methoxy-alpha- trifluoromethylphenylacetate (MTPA) Esters. J. Am. Chem. Soc. 1973, 95, 512.
-
(1973)
J. Am. Chem. Soc
, vol.95
, pp. 512
-
-
Dale, J.A.1
Mosher, H.S.2
-
31
-
-
84958315401
-
Stereoselective aldol reactions of chlorotitanium enolates - an efficient method for the assemblage of polypropionate-related synthons
-
Evans, D. A.; Rieger, D. L.; Bilodeau, M. T.; Urpi, F. Stereoselective aldol reactions of chlorotitanium enolates - an efficient method for the assemblage of polypropionate-related synthons. J. Am Chem. Soc. 1991, 113, 1047-1049.
-
(1991)
J. Am Chem. Soc
, vol.113
, pp. 1047-1049
-
-
Evans, D.A.1
Rieger, D.L.2
Bilodeau, M.T.3
Urpi, F.4
-
32
-
-
33749989298
-
Stereoselective titanium-mediated aldol reactions of (S)-2-tert-butyldimethylsilyloxy-3- pentanone
-
Nebot, J.; Figueras, S.; Romea, P.; Urpi, F.; Ji, J. Stereoselective titanium-mediated aldol reactions of (S)-2-tert-butyldimethylsilyloxy-3- pentanone. Tetrahedron 2006, 62, 11090-11099.
-
(2006)
Tetrahedron
, vol.62
, pp. 11090-11099
-
-
Nebot, J.1
Figueras, S.2
Romea, P.3
Urpi, F.4
Ji, J.5
-
33
-
-
41449100799
-
Unconventional biradical character of titanium enolates
-
Moreira, I.; De, P. R.; Bofill, J. M.; Anglada, J. M.; Solsona, J. G.; Nebot, J.; Romea, P.; Urpi, F. Unconventional biradical character of titanium enolates. J. Am. Chem. Soc. 2008, 130(11), 3242-3244.
-
(2008)
J. Am. Chem. Soc
, vol.130
, Issue.11
, pp. 3242-3244
-
-
Moreira, I.1
De, P.R.2
Bofill, J.M.3
Anglada, J.M.4
Solsona, J.G.5
Nebot, J.6
Romea, P.7
Urpi, F.8
-
34
-
-
0000376088
-
-
Carreira, E. M.; Singer, R. A.; Lee, W. Catalytic, Enantioselective aldol additions with methyl and ethyl-acetate O-silyl enolates - a chiral tridentate chelate as a ligand for titanium(IV). J. Am. Chem. Soc. 1994, 116, 8837-8838.
-
Carreira, E. M.; Singer, R. A.; Lee, W. Catalytic, Enantioselective aldol additions with methyl and ethyl-acetate O-silyl enolates - a chiral tridentate chelate as a ligand for titanium(IV). J. Am. Chem. Soc. 1994, 116, 8837-8838.
-
-
-
|