-
1
-
-
0032840976
-
Rigid and sterically regular chiral 1,10-binaphthyl polymers in asymmetric catalysis
-
Reviews: a
-
Reviews: (a) Pu, L. Rigid and sterically regular chiral 1,10-binaphthyl polymers in asymmetric catalysis. Chem. Eur. J. 1999, 5, 2227-2232;
-
(1999)
Chem. Eur. J
, vol.5
, pp. 2227-2232
-
-
Pu, L.1
-
2
-
-
0035962701
-
Polymer-supported catalysis in synthetic organic chemistry
-
(b) Clapham, B.; Reger, T. S.; Janda, K. D. Polymer-supported catalysis in synthetic organic chemistry. Tetrahedron 2001, 57, 4637-4662;
-
(2001)
Tetrahedron
, vol.57
, pp. 4637-4662
-
-
Clapham, B.1
Reger, T.S.2
Janda, K.D.3
-
3
-
-
0036811245
-
Preparation of polymer-supported ligands and metal complexes for use in catalysis
-
(c) Leadbeater, N. E.; Marco, M. Preparation of polymer-supported ligands and metal complexes for use in catalysis. Chem. Rev. 2002, 102, 3217-3273.
-
(2002)
Chem. Rev
, vol.102
, pp. 3217-3273
-
-
Leadbeater, N.E.1
Marco, M.2
-
4
-
-
0033849947
-
Soluble polymer-supported organic synthesis
-
Review
-
Review: Toy, P. H.; Janda, K. D. Soluble polymer-supported organic synthesis. Acc. Chem. Res. 2000, 33, 546-554.
-
(2000)
Acc. Chem. Res
, vol.33
, pp. 546-554
-
-
Toy, P.H.1
Janda, K.D.2
-
5
-
-
0030956225
-
-
Some selected application of poly(ethylene glycol)-supported catalysts: (a) Nandanan, E.; Sudalai, A.; Ravindranathan, T. New polymer supported cinchona alkaloids for heterogeneous catalytic asymmetric dihydroxylation of olefins. Tetrahedron Lett. 1997, 38, 2577-2580;
-
Some selected application of poly(ethylene glycol)-supported catalysts: (a) Nandanan, E.; Sudalai, A.; Ravindranathan, T. New polymer supported cinchona alkaloids for heterogeneous catalytic asymmetric dihydroxylation of olefins. Tetrahedron Lett. 1997, 38, 2577-2580;
-
-
-
-
6
-
-
0032511939
-
Expanding on the purification methodology of polyethylene glycol (PEG) bound molecules: The synthesis of 3,5-pyrazolidinediones
-
(b) Zhao, X.-Y.; Metz, W. A.; Sieber, F.; Janda, K. D. Expanding on the purification methodology of polyethylene glycol (PEG) bound molecules: The synthesis of 3,5-pyrazolidinediones. Tetrahedron Lett. 1998, 39, 8433-8436;
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 8433-8436
-
-
Zhao, X.-Y.1
Metz, W.A.2
Sieber, F.3
Janda, K.D.4
-
7
-
-
0000431168
-
A soluble polymer-bound ruthenium carbene complex: A robust and reusable catalyst for ring-closing olefin metathesis
-
(c) Yao, Q. A soluble polymer-bound ruthenium carbene complex: A robust and reusable catalyst for ring-closing olefin metathesis. Angew. Chem. 2000, 112, 4060;
-
(2000)
Angew. Chem
, vol.112
, pp. 4060
-
-
Yao, Q.1
-
9
-
-
0001682147
-
Poly(ethylene glycol)-supported proline: A versatile catalyst for the enantioselective aldol and iminoaldol reactions
-
(d) Benaglia, M.; Cinquini, M.; Cozzi, F.; Puglisi, A.; Celentano, G. Poly(ethylene glycol)-supported proline: A versatile catalyst for the enantioselective aldol and iminoaldol reactions. Adv. Synth. Catal. 2002, 344, 533-542;
-
(2002)
Adv. Synth. Catal
, vol.344
, pp. 533-542
-
-
Benaglia, M.1
Cinquini, M.2
Cozzi, F.3
Puglisi, A.4
Celentano, G.5
-
10
-
-
14644430938
-
A poly(ethylene glycol) supported chiral auxiliary for asymmetric Michael reactions
-
and references cited therein
-
(e) Kreidler, B.; Baro, A.; Christoffers, J. A poly(ethylene glycol) supported chiral auxiliary for asymmetric Michael reactions. Synlett 2005, 465-468, and references cited therein.
-
(2005)
Synlett
, pp. 465-468
-
-
Kreidler, B.1
Baro, A.2
Christoffers, J.3
-
11
-
-
4243893500
-
Selective reactions using allylic metals
-
Reviews: a
-
Reviews: (a) Yamamoto, Y.; Asao, N. Selective reactions using allylic metals. Chem. Rev. 1993, 93, 2207-2293;
-
(1993)
Chem. Rev
, vol.93
, pp. 2207-2293
-
-
Yamamoto, Y.1
Asao, N.2
-
12
-
-
2742513413
-
2-symmetric ligand for stereoselective carbon-carbon bond forming reactions
-
2-symmetric ligand for stereoselective carbon-carbon bond forming reactions. J. Prakt. Chem. 1997, 339, 758-762;
-
(1997)
J. Prakt. Chem
, vol.339
, pp. 758-762
-
-
Zimmer, R.1
Suhrbier, J.2
-
13
-
-
0000718373
-
1,1′-Binaphthyl dimers, oligomers, and polymers: Molecular recognition, asymmetric catalysis, and new materials
-
(c) Pu, L. 1,1′-Binaphthyl dimers, oligomers, and polymers: Molecular recognition, asymmetric catalysis, and new materials. Chem. Rev. 1998, 98, 2405-2494;
-
(1998)
Chem. Rev
, vol.98
, pp. 2405-2494
-
-
Pu, L.1
-
14
-
-
0042880939
-
Modified BINOL ligands in asymmetric catalysis
-
(d) Chen, Y.; Yekta, S.; Yudin, A. K. Modified BINOL ligands in asymmetric catalysis. Chem. Rev. 2003, 103, 3155-3211;
-
(2003)
Chem. Rev
, vol.103
, pp. 3155-3211
-
-
Chen, Y.1
Yekta, S.2
Yudin, A.K.3
-
15
-
-
17244369977
-
A versatile chiral reagent
-
(e) Brunel, J. M. BINOL: A versatile chiral reagent. Chem. Rev. 2005, 105, 857-897.
-
(2005)
Chem. Rev
, vol.105
, pp. 857-897
-
-
Brunel, J.1
BINOL, M.2
-
16
-
-
0000186325
-
Chiral catalyst optimization using both solid-phase and liquid-phase methods in asymmetric aza Diels-Alder reactions
-
Kobayashi, S.; Kusakabe, K.-I.; Ishitani, H. Chiral catalyst optimization using both solid-phase and liquid-phase methods in asymmetric aza Diels-Alder reactions. Org. Lett. 2000, 2, 1225-1227.
-
(2000)
Org. Lett
, vol.2
, pp. 1225-1227
-
-
Kobayashi, S.1
Kusakabe, K.-I.2
Ishitani, H.3
-
17
-
-
0034723297
-
Polymer-supported BINOL ligand for the titanium-catalyzed diethylzinc addition to aldehydes: A remarkable positive influence of the support on the enantioselectivity of the catalyst
-
(a) Yang, X.-W.; Sheng, J.-H.; Da, C.-S.; Wang, H.-S.; Su, W.; Wang, R.; Chan, A. S. C. Polymer-supported BINOL ligand for the titanium-catalyzed diethylzinc addition to aldehydes: A remarkable positive influence of the support on the enantioselectivity of the catalyst. J. Org. Chem. 2000, 65, 295-296;
-
(2000)
J. Org. Chem
, vol.65
, pp. 295-296
-
-
Yang, X.-W.1
Sheng, J.-H.2
Da, C.-S.3
Wang, H.-S.4
Su, W.5
Wang, R.6
Chan, A.S.C.7
-
18
-
-
0034717175
-
Preparation and application of polymer-grafted Ti-BINOL complexes as chiral catalysts in the enantioselective addition of diethylzinc to aldehydes
-
(b) Yang, X. W.; Su, W.; Liu, D. X.; Wang, H.-S.; Sheng, J.-H.; Da, C.-S.; Wang, R.; Chan, A. S. C. Preparation and application of polymer-grafted Ti-BINOL complexes as chiral catalysts in the enantioselective addition of diethylzinc to aldehydes. Tetrahedron 2000, 56, 3511-3516;
-
(2000)
Tetrahedron
, vol.56
, pp. 3511-3516
-
-
Yang, X.W.1
Su, W.2
Liu, D.X.3
Wang, H.-S.4
Sheng, J.-H.5
Da, C.-S.6
Wang, R.7
Chan, A.S.C.8
-
19
-
-
0035888807
-
Synthesis and catalytic applications of soluble polymer-supported BINOL
-
(c) Jayaprakash, D.; Sasai, H. Synthesis and catalytic applications of soluble polymer-supported BINOL. Tetrahedron: Asymmetry 2001, 12, 2589-2595;
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 2589-2595
-
-
Jayaprakash, D.1
Sasai, H.2
-
20
-
-
32344449946
-
Immobilization of a BINOLate-titanium catalyst by use of aggregation phenomenon
-
(d) Harada, T.; Nakatsugawa, M. Immobilization of a BINOLate-titanium catalyst by use of aggregation phenomenon. Synlett 2006, 321-323;
-
(2006)
Synlett
, pp. 321-323
-
-
Harada, T.1
Nakatsugawa, M.2
-
21
-
-
33745411906
-
Enantioselective addition of diethylzinc to aldehydes using immobilized chiral BINOL-Ti complex on ordered mesoporous silicas
-
(e) Pathak, K.; Bhatt, A. P.; Abdi, S. H. R.; Kureshy, R. I.; Khan, N.-U. H.; Ahmad, I.; Jasra, R. V. Enantioselective addition of diethylzinc to aldehydes using immobilized chiral BINOL-Ti complex on ordered mesoporous silicas. Tetrahedron: Asymmetry 2006, 17, 1506-1513.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 1506-1513
-
-
Pathak, K.1
Bhatt, A.P.2
Abdi, S.H.R.3
Kureshy, R.I.4
Khan, N.-U.H.5
Ahmad, I.6
Jasra, R.V.7
-
22
-
-
22044445168
-
Self-supported heterogeneous titanium catalysts for enantioselective carbonyl-ene and sulfoxidation reactions
-
Wang, X.; Wang, X.; Guo, H.; Wang, Z.; Ding, K. Self-supported heterogeneous titanium catalysts for enantioselective carbonyl-ene and sulfoxidation reactions. Chem. Eur. J. 2005, 11, 4078-4088.
-
(2005)
Chem. Eur. J
, vol.11
, pp. 4078-4088
-
-
Wang, X.1
Wang, X.2
Guo, H.3
Wang, Z.4
Ding, K.5
-
23
-
-
33749238329
-
An easy synthesis of robust polymer-supported chiral 1,1′-bi-(2- naphthol)s (BINOLs): Application to the catalysis of the oxidation of prochiral thioethers to chiral sulfoxides
-
Yuan, X.-Y.; Li, H.-Y.; Hodge, P.; Kilner, M.; Tastard, C. Y.; Zhang, Z.-P. An easy synthesis of robust polymer-supported chiral 1,1′-bi-(2- naphthol)s (BINOLs): Application to the catalysis of the oxidation of prochiral thioethers to chiral sulfoxides. Tetrahedron: Asymmetry 2006, 17, 2401-2407.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 2401-2407
-
-
Yuan, X.-Y.1
Li, H.-Y.2
Hodge, P.3
Kilner, M.4
Tastard, C.Y.5
Zhang, Z.-P.6
-
24
-
-
0035825054
-
Enantioselective Strecker-type reaction promoted by polymer-supported bifunctional catalyst
-
Nogami, H.; Matsunaga, S.; Kanai, M.; Shibasaki, M. Enantioselective Strecker-type reaction promoted by polymer-supported bifunctional catalyst. Tetrahedron Lett. 2001, 42, 279-283.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 279-283
-
-
Nogami, H.1
Matsunaga, S.2
Kanai, M.3
Shibasaki, M.4
-
25
-
-
14644439193
-
Synthesis of 6,6′- and 6-MeO-PEG-BINOL-Ca soluble polymer bound ligands and their application in asymmetric Michael and epoxidation reactions
-
Kumaraswamy, G.; Jena, N.; Sastry, M. N. V.; Venkata Rao, G.; Ankamma, K. Synthesis of 6,6′- and 6-MeO-PEG-BINOL-Ca soluble polymer bound ligands and their application in asymmetric Michael and epoxidation reactions. J. Mol. Catal. A 2005, 230, 59-67.
-
(2005)
J. Mol. Catal. A
, vol.230
, pp. 59-67
-
-
Kumaraswamy, G.1
Jena, N.2
Sastry, M.N.V.3
Venkata Rao, G.4
Ankamma, K.5
-
26
-
-
0038399955
-
Enantioselective epoxidation of α,β-unsaturated ketones using polymer-supported lanthanoid-BINOL complexes
-
Jayaprakash, D.; Kobayashi, Y.; Watanabe, S.; Arai, T.; Sasai, H. Enantioselective epoxidation of α,β-unsaturated ketones using polymer-supported lanthanoid-BINOL complexes. Tetrahedron: Asymmetry 2003, 14, 1587-1592.
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 1587-1592
-
-
Jayaprakash, D.1
Kobayashi, Y.2
Watanabe, S.3
Arai, T.4
Sasai, H.5
-
27
-
-
0030970084
-
An unusual selectivity in Pd catalyzed crosscoupling of terminal alkynes with "unactivated" alkynes
-
Trost, B. M.; McIntosh, M. C. An unusual selectivity in Pd catalyzed crosscoupling of terminal alkynes with "unactivated" alkynes. Tetrahedron Lett. 1997, 38, 3207-3210.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 3207-3210
-
-
Trost, B.M.1
McIntosh, M.C.2
-
28
-
-
0344074650
-
A first example of macromolecular Ti(IV) Lewis acid in the catalytic enantioselective Mukaiyama reaction
-
(a) Mandoli, A.; Pini, D.; Orlandi, S.;Mazzini, F.; Salvadori, P. A first example of macromolecular Ti(IV) Lewis acid in the catalytic enantioselective Mukaiyama reaction. Tetrahedron: Asymmetry 1998, 9, 1479-1482;
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 1479-1482
-
-
Mandoli, A.1
Pini, D.2
Orlandi, S.3
Mazzini, F.4
Salvadori, P.5
-
29
-
-
10244222363
-
Enantioselective catalysis in water: Mukaiyama-aldol condensation promoted by copper complexes of bisoxazolines supported on poly(ethylene glycol)
-
(b) Benaglia, M.; Cinquini, M.; Cozzi, F.; Celentano, G. Enantioselective catalysis in water: Mukaiyama-aldol condensation promoted by copper complexes of bisoxazolines supported on poly(ethylene glycol). Org. Biomol. Chem. 2004, 2, 3401-3407;
-
(2004)
Org. Biomol. Chem
, vol.2
, pp. 3401-3407
-
-
Benaglia, M.1
Cinquini, M.2
Cozzi, F.3
Celentano, G.4
-
30
-
-
27944434660
-
Asymmetric Mukaiyama aldol reaction of silyl enol ethers with aldehydes using a polymer-supported chiral Lewis acid catalyst
-
(c) Itsuno, S.; Arima, S.; Haraguchi, N. Asymmetric Mukaiyama aldol reaction of silyl enol ethers with aldehydes using a polymer-supported chiral Lewis acid catalyst. Tetrahedron 2005, 61, 12074-12080.
-
(2005)
Tetrahedron
, vol.61
, pp. 12074-12080
-
-
Itsuno, S.1
Arima, S.2
Haraguchi, N.3
-
31
-
-
11844259698
-
-
Mahrwald, R, Ed, Wiley-VCH: Weinheim
-
Mahrwald, R. (Ed.). Modern Aldol Reaction; Wiley-VCH: Weinheim, 2004.
-
(2004)
Modern Aldol Reaction
-
-
-
32
-
-
0000013894
-
-
Keck, G. E.; Krishnamurthy, D. Pronounced solvent and concentration effects in an enantioselective Mukaiyama aldol condensation using BINOL-titanium(IV) catalysts. J. Am. Chem. Soc. 1995, 117, 2363-2364.
-
Keck, G. E.; Krishnamurthy, D. Pronounced solvent and concentration effects in an enantioselective Mukaiyama aldol condensation using BINOL-titanium(IV) catalysts. J. Am. Chem. Soc. 1995, 117, 2363-2364.
-
-
-
-
33
-
-
0001087242
-
Asymmetric catalytic aldol-type reaction with ketene silyl acetals - Possible intervention of the silatropic ene pathway
-
Mikami, K.; Matsukawa, S. Asymmetric catalytic aldol-type reaction with ketene silyl acetals - Possible intervention of the silatropic ene pathway. J. Am. Chem. Soc. 1994, 116, 4077-4078.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 4077-4078
-
-
Mikami, K.1
Matsukawa, S.2
-
34
-
-
0028844801
-
Highly enantioselective catalysis of the Mukaiyama aldol reaction by BINOL-Ti perfluorophenoxide and enoxysilacyclobutane
-
Matsukawa, S.; Mikami, K. Highly enantioselective catalysis of the Mukaiyama aldol reaction by BINOL-Ti perfluorophenoxide and enoxysilacyclobutane. Tetrahedron: Asymmetry 1995, 6, 2571-2574.
-
(1995)
Tetrahedron: Asymmetry
, vol.6
, pp. 2571-2574
-
-
Matsukawa, S.1
Mikami, K.2
-
35
-
-
2742513913
-
Asymmetric catalysis of the Mukaiyama aldol reaction with fluoral - A highly enantioselctive access to fluorine-containing aldols
-
Mikami, K.; Takasaki, T.; Matsukawa, S.; Maruta, M. Asymmetric catalysis of the Mukaiyama aldol reaction with fluoral - A highly enantioselctive access to fluorine-containing aldols. Synlett 1995, 1057.
-
(1995)
Synlett
, pp. 1057
-
-
Mikami, K.1
Takasaki, T.2
Matsukawa, S.3
Maruta, M.4
-
36
-
-
0029656027
-
Asymmetric catalysis of carbonyl-ene and aldol reactions with fluoral by chiral binaphthol-derived titanium complex
-
Mikami, K.; Yajima, T.; Takasaki, T.; Matsukawa, S.; Terada, M.; Uchimaru, T.; Maruta, M. Asymmetric catalysis of carbonyl-ene and aldol reactions with fluoral by chiral binaphthol-derived titanium complex. Tetrahedron 1996, 52, 85-98.
-
(1996)
Tetrahedron
, vol.52
, pp. 85-98
-
-
Mikami, K.1
Yajima, T.2
Takasaki, T.3
Matsukawa, S.4
Terada, M.5
Uchimaru, T.6
Maruta, M.7
-
37
-
-
0002227151
-
Chiral drugging: Chiral activator-induced enantiomer selective activation of racemic catalyst for asymmetric amplifying catalysis
-
Matsukawa, S.; Mikami, K. Chiral drugging: Chiral activator-induced enantiomer selective activation of racemic catalyst for asymmetric amplifying catalysis. Enantiomer 1996, 1, 69-73.
-
(1996)
Enantiomer
, vol.1
, pp. 69-73
-
-
Matsukawa, S.1
Mikami, K.2
-
38
-
-
0031575791
-
Asymmetric carbonyl addition reactions to benzyloxyaldehydes by binaphthol-titanium catalyst: Anti- vs. syn-diastereofacial preference in anomalous nonchelation complexation
-
Mikami, K.; Matsukawa, S.; Sawa, E.; Harada, A.; Koga, N. Asymmetric carbonyl addition reactions to benzyloxyaldehydes by binaphthol-titanium catalyst: Anti- vs. syn-diastereofacial preference in anomalous nonchelation complexation. Tetrahedron Lett. 1997, 38, 1951-1954.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 1951-1954
-
-
Mikami, K.1
Matsukawa, S.2
Sawa, E.3
Harada, A.4
Koga, N.5
-
39
-
-
0034616874
-
Highly anti-selective catalytic asymmetric aldol reactions
-
Ishitani, H.; Yamashita, Y.; Shimizu, H.; Kobayashi, S. Highly anti-selective catalytic asymmetric aldol reactions. J. Am. Chem. Soc. 2000, 122, 5403-5404.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 5403-5404
-
-
Ishitani, H.1
Yamashita, Y.2
Shimizu, H.3
Kobayashi, S.4
-
40
-
-
0036774726
-
Optimisation, scope and limitations of enantioselective aldol reactions of an S-ketene silyl acetal with aliphatic aldehydes under (R)-BINOL-titanium(IV) catalysis conditions
-
Zimmer, R.; Peritz, A.; Czerwonka, R.; Schefzig, L.; Reissig, H.-U. Optimisation, scope and limitations of enantioselective aldol reactions of an S-ketene silyl acetal with aliphatic aldehydes under (R)-BINOL-titanium(IV) catalysis conditions. Eur. J. Org. Chem. 2002, 3419-3428.
-
(2002)
Eur. J. Org. Chem
, pp. 3419-3428
-
-
Zimmer, R.1
Peritz, A.2
Czerwonka, R.3
Schefzig, L.4
Reissig, H.-U.5
-
41
-
-
3042707283
-
Functionalized BINOL derivatives as ligands for enantioselectively catalyzed aldol additions: Highly enantioselective synthesis of chiral β-hydroxy thioesters
-
Zimmer, R.; Schefzig, L.; Peritz, A.; Dekaris, V.; Reissig, H.-U. Functionalized BINOL derivatives as ligands for enantioselectively catalyzed aldol additions: Highly enantioselective synthesis of chiral β-hydroxy thioesters. Synthesis 2004, 1439-1445.
-
(2004)
Synthesis
, pp. 1439-1445
-
-
Zimmer, R.1
Schefzig, L.2
Peritz, A.3
Dekaris, V.4
Reissig, H.-U.5
-
42
-
-
0034684178
-
Application of complex aldol reactions to the total synthesis of phorboxazole B
-
Evans, D. A.; Fitch, D. M.; Smith, T. E.; Cee, V. J. Application of complex aldol reactions to the total synthesis of phorboxazole B. J. Am. Chem. Soc. 2000, 122, 10033-10046.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 10033-10046
-
-
Evans, D.A.1
Fitch, D.M.2
Smith, T.E.3
Cee, V.J.4
-
43
-
-
0034693109
-
Combinatorial liquid-phase synthesis of [1,4]oxazepine-7-ones via the Baylis-Hillman reaction
-
Räcker, R.; Döring, K.; Reiser, O. Combinatorial liquid-phase synthesis of [1,4]oxazepine-7-ones via the Baylis-Hillman reaction. J. Org. Chem. 2000, 65, 6932-6939.
-
(2000)
J. Org. Chem
, vol.65
, pp. 6932-6939
-
-
Räcker, R.1
Döring, K.2
Reiser, O.3
-
44
-
-
0037182223
-
Efficient synthesis of 6-mono-bromo-1,1′-bi-2-naphthol
-
(a) Cai, D.; Larsen, R. D.; Reider, P. J. Efficient synthesis of 6-mono-bromo-1,1′-bi-2-naphthol. Tetrahedron Lett. 2002, 43, 4055-4057;
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 4055-4057
-
-
Cai, D.1
Larsen, R.D.2
Reider, P.J.3
-
45
-
-
0037467687
-
A simple synthetic approach to homochiral 6-and 6′-substituted 1,1′-binaphthyl derivatives
-
(b) Hocke, H.; Uozumi, Y. A simple synthetic approach to homochiral 6-and 6′-substituted 1,1′-binaphthyl derivatives. Tetrahedron 2003, 59, 619-630.
-
(2003)
Tetrahedron
, vol.59
, pp. 619-630
-
-
Hocke, H.1
Uozumi, Y.2
-
46
-
-
0343456237
-
Host-guest complexation 14: Host covalently bound to polystyrene resin for chromatographic resolution of enantiomers of amino acid and ester salts
-
Dotsevi Yao Sogah, G.; Cram, D. J. Host-guest complexation 14: Host covalently bound to polystyrene resin for chromatographic resolution of enantiomers of amino acid and ester salts. J. Am. Chem. Soc. 1979, 101, 3035-3042;
-
(1979)
J. Am. Chem. Soc
, vol.101
, pp. 3035-3042
-
-
Dotsevi Yao Sogah, G.1
Cram, D.J.2
-
47
-
-
33751386025
-
Catalytic asymmetric allylation reactions 3: Extension to methallylstannane, comparison of procedures, and observation of a nonlinar effect
-
Keck, G. E.; Krishnamurthy, D.; Grier, M. C. Catalytic asymmetric allylation reactions 3: Extension to methallylstannane, comparison of procedures, and observation of a nonlinar effect. J. Org. Chem. 1993, 58, 6543-6544.
-
(1993)
J. Org. Chem
, vol.58
, pp. 6543-6544
-
-
Keck, G.E.1
Krishnamurthy, D.2
Grier, M.C.3
-
48
-
-
0001684888
-
Asymmetric activation
-
Review on asymmetric activation
-
Review on asymmetric activation: Mikami, K.; Terada, M.; Korenaga, T.; Matsumoto, Y.; Ueki, M.; Angelaud, R. Asymmetric activation. Angew. Chem. 2000, 112, 3676-3701;
-
(2000)
Angew. Chem
, vol.112
, pp. 3676-3701
-
-
Mikami, K.1
Terada, M.2
Korenaga, T.3
Matsumoto, Y.4
Ueki, M.5
Angelaud, R.6
-
49
-
-
0034675555
-
-
Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
-
(2000)
Angew. Chem. Int. Ed
, vol.39
, pp. 3532-3556
-
-
-
50
-
-
0037458692
-
-
4 catalyst with phenolic additives for the enantioselective alkynylation of aldehydes. Tetrahedron: Asymmetry 2003, 14, 449-452.
-
4 catalyst with phenolic additives for the enantioselective alkynylation of aldehydes. Tetrahedron: Asymmetry 2003, 14, 449-452.
-
-
-
-
51
-
-
0001842782
-
-
With molecular sieves; (b) Terada, M, Matsumoto, Y, Nakamura, Y, Mikami, K. Anomalous role of molecular sieves 4Å in the preparation of a binaphthol-derived active μ3-oxo titanium catalyst. Chem. Commun. 1997, 281-282
-
3-oxo titanium catalyst. Chem. Commun. 1997, 281-282.
-
-
-
-
52
-
-
60849126290
-
-
With alcohols; (c) Waltz, K. M.; Gavenonis, J.; Walsh, P. J. A simple, reliable, catalytic asymmetric allylation of ketones. Angew. Chem. 2002, 114, 3849-3852;
-
With alcohols; (c) Waltz, K. M.; Gavenonis, J.; Walsh, P. J. A simple, reliable, catalytic asymmetric allylation of ketones. Angew. Chem. 2002, 114, 3849-3852;
-
-
-
-
53
-
-
0037020373
-
-
Angew. Chem. Int. Ed. 2002, 41, 3697-3699.
-
(2002)
Angew. Chem. Int. Ed
, vol.41
, pp. 3697-3699
-
-
-
54
-
-
0001588160
-
Self-assembly of several components into a highly enantioselective Ti catalyst for carbonyl-ene reactions
-
For chiral activators, see
-
For chiral activators, see Mikami, K.; Matsukawa, S.; Volk, T.; Terada, M. Self-assembly of several components into a highly enantioselective Ti catalyst for carbonyl-ene reactions. Angew. Chem. 1997, 109, 2936-2939;
-
(1997)
Angew. Chem
, vol.109
, pp. 2936-2939
-
-
Mikami, K.1
Matsukawa, S.2
Volk, T.3
Terada, M.4
-
56
-
-
33745728242
-
-
Application of chiral ionic liquid: Martin, D.; Kehrli, S.; D'Augustin, M.; Clavier, H.; Mauduit, M.; Alexakis, A. Copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted enones: Construction of all-carbon quaternary chiral centers. J. Am. Chem. Soc. 2006, 128, 8416-8417.
-
Application of chiral ionic liquid: Martin, D.; Kehrli, S.; D'Augustin, M.; Clavier, H.; Mauduit, M.; Alexakis, A. Copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted enones: Construction of all-carbon quaternary chiral centers. J. Am. Chem. Soc. 2006, 128, 8416-8417.
-
-
-
-
57
-
-
33846376783
-
Functionalized ionic liquids catalyzed direct aldol reactions
-
For catalyzed direct aldol reactions, see
-
For catalyzed direct aldol reactions, see Luo, S.; Mi, X.; Zhang, L.; Liu, S.; Xu, H.; Cheng, J.-P. Functionalized ionic liquids catalyzed direct aldol reactions. Tetrahedron 2007, 59, 1923-1930.
-
(2007)
Tetrahedron
, vol.59
, pp. 1923-1930
-
-
Luo, S.1
Mi, X.2
Zhang, L.3
Liu, S.4
Xu, H.5
Cheng, J.-P.6
-
58
-
-
0030734711
-
A bis-steroidal phosphine as new chiral hydrogenation ligand
-
(a) Enev, V.; Ewers, C. L. J.; Harre, M.; Nickisch, K.; Mohr, J. T. A bis-steroidal phosphine as new chiral hydrogenation ligand. J. Org. Chem. 1997, 62, 7092-7093;
-
(1997)
J. Org. Chem
, vol.62
, pp. 7092-7093
-
-
Enev, V.1
Ewers, C.L.J.2
Harre, M.3
Nickisch, K.4
Mohr, J.T.5
-
59
-
-
0037175460
-
A new family of substituted steroidal BINOL-type ligands
-
(b) Schneider, M. F.; Harre, M.; Pieper, C. A new family of substituted steroidal BINOL-type ligands. Tetrahedron Lett. 2002, 43, 8751-8754.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 8751-8754
-
-
Schneider, M.F.1
Harre, M.2
Pieper, C.3
-
60
-
-
0010640653
-
α-Methoxy-α- trifluoromethylphenylacetic acid, a versatile reagent for determination of enantiomeric composition of alcohols and amines
-
Dale, J. A.; Dull, D. L.; Mosher, H. S. α-Methoxy-α- trifluoromethylphenylacetic acid, a versatile reagent for determination of enantiomeric composition of alcohols and amines. J. Org. Chem. 1969, 34, 2543.
-
(1969)
J. Org. Chem
, vol.34
, pp. 2543
-
-
Dale, J.A.1
Dull, D.L.2
Mosher, H.S.3
-
61
-
-
33746512827
-
Michael addition of carbothioates - Application to synthesis of (+/-)-jasmine ketolactone
-
Gerlach, H.; Künzler, P. Michael addition of carbothioates - Application to synthesis of (+/-)-jasmine ketolactone. Helv. Chim. Acta 1978, 61, 2503-2509.
-
(1978)
Helv. Chim. Acta
, vol.61
, pp. 2503-2509
-
-
Gerlach, H.1
Künzler, P.2
-
62
-
-
0034629447
-
Enantioselective synthesis of (S)- and (R)-6-hydroxy-8-nonene- carboxylates by asymmetric catalysis: α-lipoic acid and its (S)-antipode
-
Zimmer, R.; Hain, U.; Berndt, M.; Gewald, R.; Reissig, H.-U. Enantioselective synthesis of (S)- and (R)-6-hydroxy-8-nonene- carboxylates by asymmetric catalysis: α-lipoic acid and its (S)-antipode. Tetrahedron: Asymmetry 2000, 11, 879-887.
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 879-887
-
-
Zimmer, R.1
Hain, U.2
Berndt, M.3
Gewald, R.4
Reissig, H.-U.5
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