-
1
-
-
2342570203
-
Enantioselective Mannich-Type Reaction Catalyzed by a Chiral Brønsted Acid
-
Akiyama, T.; Itoh, J.; Yokota, K.; Fuchibe, K. Enantioselective Mannich-Type Reaction Catalyzed by a Chiral Brønsted Acid Angew. Chem., Int. Ed. 2004, 43, 1566-1568
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1566-1568
-
-
Akiyama, T.1
Itoh, J.2
Yokota, K.3
Fuchibe, K.4
-
2
-
-
2342521907
-
Chiral Brønsted Acid-Catalyzed Direct Mannich Reactions via Electrophilic Activation
-
Uraguchi, D.; Terada, M. Chiral Brønsted Acid-Catalyzed Direct Mannich Reactions via Electrophilic Activation J. Am. Chem. Soc. 2004, 126, 5356-5357
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 5356-5357
-
-
Uraguchi, D.1
Terada, M.2
-
3
-
-
38349189109
-
Stronger Brønsted Acids
-
Akiyama, T. Stronger Brønsted Acids Chem. Rev. 2007, 107, 5744-5758
-
(2007)
Chem. Rev.
, vol.107
, pp. 5744-5758
-
-
Akiyama, T.1
-
4
-
-
51049088569
-
A powerful Brønsted acid catalyst for asymmetric synthesis
-
Adair, G.; Mukherjee, S.; List, B. A powerful Brønsted acid catalyst for asymmetric synthesis Aldrichim. Acta 2008, 42, 31-39
-
(2008)
Aldrichim. Acta
, vol.42
, pp. 31-39
-
-
Adair, G.1
Mukherjee, S.2
List, B.3
-
5
-
-
77950261392
-
Chiral Brønsted Acids for Asymmetric Organocatalysis
-
List, B. Springer: Berlin/Heidelberg, Germany
-
Kampen, D.; Reisinger, C. M.; List, B. Chiral Brønsted Acids for Asymmetric Organocatalysis. In Asymmetric Organocatalysis; List, B., Ed.; Springer: Berlin/Heidelberg, Germany, 2009; Vol. 291, pp 1-37.
-
(2009)
Asymmetric Organocatalysis
, vol.291
, pp. 1-37
-
-
Kampen, D.1
Reisinger, C.M.2
List, B.3
-
6
-
-
84908249055
-
Complete Field Guide to Asymmetric BINOL-Phosphate Derived Brønsted Acid and Metal Catalysis: History and Classification by Mode of Activation; Brønsted Acidity, Hydrogen Bonding, Ion Pairing, and Metal Phosphates
-
Parmar, D.; Sugiono, E.; Raja, S.; Rueping, M. Complete Field Guide to Asymmetric BINOL-Phosphate Derived Brønsted Acid and Metal Catalysis: History and Classification by Mode of Activation; Brønsted Acidity, Hydrogen Bonding, Ion Pairing, and Metal Phosphates Chem. Rev. 2014, 114, 9047-9153
-
(2014)
Chem. Rev.
, vol.114
, pp. 9047-9153
-
-
Parmar, D.1
Sugiono, E.2
Raja, S.3
Rueping, M.4
-
7
-
-
84864186595
-
Double axially chiral bisphosphorylimides as novel Brønsted acids in asymmetric three-component Mannich reaction
-
Chen, Y.-Y.; Jiang, Y.-J.; Fan, Y.-S.; Sha, D.; Wang, Q.; Zhang, G.; Zheng, L.; Zhang, S. Double axially chiral bisphosphorylimides as novel Brønsted acids in asymmetric three-component Mannich reaction Tetrahedron: Asymmetry 2012, 23, 904-909
-
(2012)
Tetrahedron: Asymmetry
, vol.23
, pp. 904-909
-
-
Chen, Y.-Y.1
Jiang, Y.-J.2
Fan, Y.-S.3
Sha, D.4
Wang, Q.5
Zhang, G.6
Zheng, L.7
Zhang, S.8
-
8
-
-
84858257928
-
Asymmetric spiroacetalization catalysed by confined Brønsted acids
-
Čorić, I.; List, B. Asymmetric spiroacetalization catalysed by confined Brønsted acids Nature 2012, 483, 315-319
-
(2012)
Nature
, vol.483
, pp. 315-319
-
-
Čorić, I.1
List, B.2
-
9
-
-
84863521201
-
2 by Chiral Confined Brønsted Acids: A Highly Enantioselective Catalytic Sulfoxidation
-
2 by Chiral Confined Brønsted Acids: A Highly Enantioselective Catalytic Sulfoxidation J. Am. Chem. Soc. 2012, 134, 10765-10768
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 10765-10768
-
-
Liao, S.1
Čorić, I.2
Wang, Q.3
List, B.4
-
10
-
-
84870689663
-
Developing Catalytic Asymmetric Acetalizations
-
Gooßen, L. J. Springer: Berlin/Heidelberg, Germany
-
Čorić, I.; Vellalath, S.; Müller, S.; Cheng, X.; List, B., Developing Catalytic Asymmetric Acetalizations. In Inventing Reactions; Gooßen, L. J., Ed.; Springer: Berlin/Heidelberg, Germany, 2013; Vol. 44, pp 165-193.
-
(2013)
Inventing Reactions
, vol.44
, pp. 165-193
-
-
Čorić, I.1
Vellalath, S.2
Müller, S.3
Cheng, X.4
List, B.5
-
11
-
-
84876245033
-
The Catalytic Asymmetric Acetalization
-
Kim, J. H.; Čorić, I.; Vellalath, S.; List, B. The Catalytic Asymmetric Acetalization Angew. Chem., Int. Ed. 2013, 52, 4474-4477
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 4474-4477
-
-
Kim, J.H.1
Čorić, I.2
Vellalath, S.3
List, B.4
-
12
-
-
84871951289
-
Double Axially Chiral Bisphosphorylimides Catalyzed Highly Enantioselective and Efficient Friedel-Crafts Reaction of Indoles with Imines
-
Wu, K.; Jiang, Y.-J.; Fan, Y.-S.; Sha, D.; Zhang, S. Double Axially Chiral Bisphosphorylimides Catalyzed Highly Enantioselective and Efficient Friedel-Crafts Reaction of Indoles with Imines Chem.-Eur. J. 2013, 19, 474-478
-
(2013)
Chem.-Eur. J.
, vol.19
, pp. 474-478
-
-
Wu, K.1
Jiang, Y.-J.2
Fan, Y.-S.3
Sha, D.4
Zhang, S.5
-
13
-
-
84894524215
-
Enantioselective Synthesis of Triarylmethanes by Chiral Imidodiphosphoric Acids Catalyzed Friedel-Crafts Reactions
-
Zhuo, M.-H.; Jiang, Y.-J.; Fan, Y.-S.; Gao, Y.; Liu, S.; Zhang, S. Enantioselective Synthesis of Triarylmethanes by Chiral Imidodiphosphoric Acids Catalyzed Friedel-Crafts Reactions Org. Lett. 2014, 16, 1096-1099
-
(2014)
Org. Lett.
, vol.16
, pp. 1096-1099
-
-
Zhuo, M.-H.1
Jiang, Y.-J.2
Fan, Y.-S.3
Gao, Y.4
Liu, S.5
Zhang, S.6
-
14
-
-
79952855341
-
Super Brønsted acid catalysis
-
Cheon, C. H.; Yamamoto, H. Super Brønsted acid catalysis Chem. Commun. 2011, 47, 3043-3056
-
(2011)
Chem. Commun.
, vol.47
, pp. 3043-3056
-
-
Cheon, C.H.1
Yamamoto, H.2
-
15
-
-
79960219398
-
Modulating the Acidity: Highly Acidic Brønsted Acids in Asymmetric Catalysis
-
Rueping, M.; Nachtsheim, B. J.; Ieawsuwan, W.; Atodiresei, I. Modulating the Acidity: Highly Acidic Brønsted Acids in Asymmetric Catalysis Angew. Chem., Int. Ed. 2011, 50, 6706-6720
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 6706-6720
-
-
Rueping, M.1
Nachtsheim, B.J.2
Ieawsuwan, W.3
Atodiresei, I.4
-
16
-
-
33746654536
-
Design of Chiral N-Triflyl Phosphoramide as a Strong Chiral Brønsted Acid and Its Application to Asymmetric Diels-Alder Reaction
-
Nakashima, D.; Yamamoto, H. Design of Chiral N-Triflyl Phosphoramide as a Strong Chiral Brønsted Acid and Its Application to Asymmetric Diels-Alder Reaction J. Am. Chem. Soc. 2006, 128, 9626-9627
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 9626-9627
-
-
Nakashima, D.1
Yamamoto, H.2
-
17
-
-
58049202980
-
Pyridinium 1,1′-Binaphthyl-2,2′-disulfonates as Highly Effective Chiral Brønsted Acid-Base Combined Salt Catalysts for Enantioselective Mannich-Type Reaction
-
Hatano, M.; Maki, T.; Moriyama, K.; Arinobe, M.; Ishihara, K. Pyridinium 1,1′-Binaphthyl-2,2′-disulfonates as Highly Effective Chiral Brønsted Acid-Base Combined Salt Catalysts for Enantioselective Mannich-Type Reaction J. Am. Chem. Soc. 2008, 130, 16858-16860
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 16858-16860
-
-
Hatano, M.1
Maki, T.2
Moriyama, K.3
Arinobe, M.4
Ishihara, K.5
-
18
-
-
52149105532
-
Brønsted Acid-Catalyzed Three-Component Hosomi-Sakurai Reactions
-
Kampen, D.; Ladépêche, A.; Claßen, G.; List, B. Brønsted Acid-Catalyzed Three-Component Hosomi-Sakurai Reactions Adv. Synth. Catal. 2008, 350, 962-966
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 962-966
-
-
Kampen, D.1
Ladépêche, A.2
Claßen, G.3
List, B.4
-
19
-
-
40149102853
-
The Catalytic Acylcyanation of Imines
-
Pan, S. C.; List, B. The Catalytic Acylcyanation of Imines Chem.-Asian J. 2008, 3, 430-437
-
(2008)
Chem.-Asian J.
, vol.3
, pp. 430-437
-
-
Pan, S.C.1
List, B.2
-
20
-
-
70349785016
-
A Powerful Chiral Counteranion Motif for Asymmetric Catalysis
-
García-García, P.; Lay, F.; García-García, P.; Rabalakos, C.; List, B. A Powerful Chiral Counteranion Motif for Asymmetric Catalysis Angew. Chem., Int. Ed. 2009, 48, 4363-4366
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 4363-4366
-
-
García-García, P.1
Lay, F.2
García-García, P.3
Rabalakos, C.4
List, B.5
-
21
-
-
77956485890
-
Synthesis and Structural Characterization of a New Class of Strong Chiral Brønsted Acids: 1,1′-Binaphthyl-2,2′-bis(sulfuryl)imides (JINGLEs)
-
Berkessel, A.; Christ, P.; Leconte, N.; Neudörfl, J.-M.; Schäfer, M. Synthesis and Structural Characterization of a New Class of Strong Chiral Brønsted Acids: 1,1′-Binaphthyl-2,2′-bis(sulfuryl)imides (JINGLEs) Eur. J. Org. Chem. 2010, 5165-5170
-
(2010)
Eur. J. Org. Chem.
, pp. 5165-5170
-
-
Berkessel, A.1
Christ, P.2
Leconte, N.3
Neudörfl, J.-M.4
Schäfer, M.5
-
22
-
-
79960536604
-
a Values of Chiral Brønsted Acid Catalysts: Phosphoric Acids/Amides, Sulfonyl/Sulfuryl Imides, and Perfluorinated TADDOLs (TEFDDOLs)
-
a Values of Chiral Brønsted Acid Catalysts: Phosphoric Acids/Amides, Sulfonyl/Sulfuryl Imides, and Perfluorinated TADDOLs (TEFDDOLs) Chem.-Eur. J. 2011, 17, 8524-8528
-
(2011)
Chem.-Eur. J.
, vol.17
, pp. 8524-8528
-
-
Christ, P.1
Lindsay, A.G.2
Vormittag, S.S.3
Neudörfl, J.-M.4
Berkessel, A.5
ODonoghue, A.C.6
-
23
-
-
84886007342
-
On the Acidity and Reactivity of Highly Effective Chiral Brønsted Acid Catalysts: Establishment of an Acidity Scale
-
Kaupmees, K.; Tolstoluzhsky, N.; Raja, S.; Rueping, M.; Leito, I. On the Acidity and Reactivity of Highly Effective Chiral Brønsted Acid Catalysts: Establishment of an Acidity Scale Angew. Chem., Int. Ed. 2013, 52, 11569-11572
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 11569-11572
-
-
Kaupmees, K.1
Tolstoluzhsky, N.2
Raja, S.3
Rueping, M.4
Leito, I.5
-
24
-
-
84880547246
-
Theoretical Study on the Acidities of Chiral Phosphoric Acids in Dimethyl Sulfoxide: Hints for Organocatalysis
-
Yang, C.; Xue, X.-S.; Jin, J.-L.; Li, X.; Cheng, J.-P. Theoretical Study on the Acidities of Chiral Phosphoric Acids in Dimethyl Sulfoxide: Hints for Organocatalysis J. Org. Chem. 2013, 78, 7076-7085
-
(2013)
J. Org. Chem.
, vol.78
, pp. 7076-7085
-
-
Yang, C.1
Xue, X.-S.2
Jin, J.-L.3
Li, X.4
Cheng, J.-P.5
-
25
-
-
84900852336
-
Computational Study on the Acidic Constants of Chiral Brønsted Acids in Dimethyl Sulfoxide
-
Yang, C.; Xue, X.-S.; Li, X.; Cheng, J.-P. Computational Study on the Acidic Constants of Chiral Brønsted Acids in Dimethyl Sulfoxide J. Org. Chem. 2014, 79, 4340-4351
-
(2014)
J. Org. Chem.
, vol.79
, pp. 4340-4351
-
-
Yang, C.1
Xue, X.-S.2
Li, X.3
Cheng, J.-P.4
-
26
-
-
79957510172
-
Enantioselective Friedel-Crafts Aminoalkylation Catalyzed by Chiral Ammonium 1,1′-Binaphthyl-2,2′-disulfonates
-
Hatano, M.; Sugiura, Y.; Akakura, M.; Ishihara, K. Enantioselective Friedel-Crafts Aminoalkylation Catalyzed by Chiral Ammonium 1,1′-Binaphthyl-2,2′-disulfonates Synlett 2011, 1247-1250
-
(2011)
Synlett
, pp. 1247-1250
-
-
Hatano, M.1
Sugiura, Y.2
Akakura, M.3
Ishihara, K.4
-
27
-
-
84860336485
-
Enantioselective direct aminalization with primary carboxamides catalyzed by chiral ammonium 1,1′-binaphthyl-2,2′-disulfonates
-
Hatano, M.; Ozaki, T.; Sugiura, Y.; Ishihara, K. Enantioselective direct aminalization with primary carboxamides catalyzed by chiral ammonium 1,1′-binaphthyl-2,2′-disulfonates Chem. Commun. 2012, 48, 4986-4988
-
(2012)
Chem. Commun.
, vol.48
, pp. 4986-4988
-
-
Hatano, M.1
Ozaki, T.2
Sugiura, Y.3
Ishihara, K.4
-
28
-
-
84899016139
-
Chiral 1,1′-Binaphthyl-2,2′-Disulfonic Acid (BINSA) and Its Derivatives for Asymmetric Catalysis
-
Hatano, M.; Ishihara, K. Chiral 1,1′-Binaphthyl-2,2′-Disulfonic Acid (BINSA) and Its Derivatives for Asymmetric Catalysis Asian J. Org. Chem. 2014, 3, 352-365
-
(2014)
Asian J. Org. Chem.
, vol.3
, pp. 352-365
-
-
Hatano, M.1
Ishihara, K.2
-
29
-
-
77953570285
-
ACDC-Nicht nur für Heavy-Metal-Fans
-
Ratjen, L.; Müller, S.; List, B. ACDC-Nicht nur für Heavy-Metal-Fans Nachr. Chem. 2010, 58, 640-646
-
(2010)
Nachr. Chem.
, vol.58
, pp. 640-646
-
-
Ratjen, L.1
Müller, S.2
List, B.3
-
30
-
-
84864271772
-
Asymmetric Counteranion-Directed Catalysis (ACDC): A Remarkably General Approach to Enantioselective Synthesis
-
Mahlau, M.; List, B. Asymmetric Counteranion-Directed Catalysis (ACDC): A Remarkably General Approach to Enantioselective Synthesis Isr. J. Chem. 2012, 52, 630-638
-
(2012)
Isr. J. Chem.
, vol.52
, pp. 630-638
-
-
Mahlau, M.1
List, B.2
-
31
-
-
84886342610
-
Asymmetric Counteranion-Directed Catalysis (ACDC)
-
Christmann, M. Bräse, S. Wiley-VCH: Weinheim, Germany
-
Mahlau, M.; List, B. Asymmetric Counteranion-Directed Catalysis (ACDC). In Asymmetric Synthesis II: More Methods and Applications; Christmann, M.; Bräse, S., Eds.; Wiley-VCH: Weinheim, Germany, 2012; pp 79-84.
-
(2012)
Asymmetric Synthesis II: More Methods and Applications
, pp. 79-84
-
-
Mahlau, M.1
List, B.2
-
32
-
-
84864370494
-
The progression of chiral anions from concepts to applications in asymmetric catalysis
-
Phipps, R. J.; Hamilton, G. L.; Toste, F. D. The progression of chiral anions from concepts to applications in asymmetric catalysis Nat. Chem. 2012, 4, 603-614
-
(2012)
Nat. Chem.
, vol.4
, pp. 603-614
-
-
Phipps, R.J.1
Hamilton, G.L.2
Toste, F.D.3
-
33
-
-
84871966452
-
Asymmetric Ion-Pairing Catalysis
-
Brak, K.; Jacobsen, E. N. Asymmetric Ion-Pairing Catalysis Angew. Chem., Int. Ed. 2013, 52, 534-561
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 534-561
-
-
Brak, K.1
Jacobsen, E.N.2
-
34
-
-
84872002336
-
Asymmetric Counteranion-Directed Catalysis: Concept, Definition, and Applications
-
Mahlau, M.; List, B. Asymmetric Counteranion-Directed Catalysis: Concept, Definition, and Applications Angew. Chem., Int. Ed. 2013, 52, 518-533
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 518-533
-
-
Mahlau, M.1
List, B.2
-
35
-
-
0000103208
-
Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent
-
Noyori, R.; Tomino, I.; Tanimoto, Y. Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent J. Am. Chem. Soc. 1979, 101, 3129-3131
-
(1979)
J. Am. Chem. Soc.
, vol.101
, pp. 3129-3131
-
-
Noyori, R.1
Tomino, I.2
Tanimoto, Y.3
-
36
-
-
0037436454
-
Privileged Chiral Catalysts
-
Yoon, T. P.; Jacobsen, E. N. Privileged Chiral Catalysts Science 2003, 299, 1691-1693
-
(2003)
Science
, vol.299
, pp. 1691-1693
-
-
Yoon, T.P.1
Jacobsen, E.N.2
-
37
-
-
84875216725
-
Catalytic properties and acidity of 1,2-benzenedisulfonimide and some of its derivatives. An experimental and computational study
-
Barbero, M.; Berto, S.; Cadamuro, S.; Daniele, P. G.; Dughera, S.; Ghigo, G. Catalytic properties and acidity of 1,2-benzenedisulfonimide and some of its derivatives. An experimental and computational study Tetrahedron 2013, 69, 3212-3217
-
(2013)
Tetrahedron
, vol.69
, pp. 3212-3217
-
-
Barbero, M.1
Berto, S.2
Cadamuro, S.3
Daniele, P.G.4
Dughera, S.5
Ghigo, G.6
-
38
-
-
67650689321
-
BINBAM-A New Motif for Strong and Chiral Brønsted Acids
-
Treskow, M.; Neudörfl, J.; Giernoth, R. BINBAM-A New Motif for Strong and Chiral Brønsted Acids Eur. J. Org. Chem. 2009, 3693-3697
-
(2009)
Eur. J. Org. Chem.
, pp. 3693-3697
-
-
Treskow, M.1
Neudörfl, J.2
Giernoth, R.3
-
39
-
-
85042961345
-
-
PhD Thesis; Universität zu Köln, Köln, Germany
-
Hoffmann, S. PhD Thesis; Universität zu Köln, Köln, Germany, 2008.
-
(2008)
-
-
Hoffmann, S.1
-
40
-
-
84860783753
-
O-Benzenedisulfonimide and its chiral derivative as Brønsted acids catalysts for one-pot three-component Strecker reaction. Synthetic and mechanistic aspects
-
Barbero, M.; Cadamuro, S.; Dughera, S.; Ghigo, G. o-Benzenedisulfonimide and its chiral derivative as Brønsted acids catalysts for one-pot three-component Strecker reaction. Synthetic and mechanistic aspects Org. Biomol. Chem. 2012, 10, 4058-4068
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 4058-4068
-
-
Barbero, M.1
Cadamuro, S.2
Dughera, S.3
Ghigo, G.4
-
41
-
-
84901264448
-
Chiral derivatives of 1,2-benzenedisulfonimide as efficient Brønsted acid catalysts in the Strecker reaction
-
Dughera, S.; Barbero, M.; Cadamuro, S.; Torregrossa, R. Chiral derivatives of 1,2-benzenedisulfonimide as efficient Brønsted acid catalysts in the Strecker reaction Org. Biomol. Chem. 2014, 12, 3902-3911
-
(2014)
Org. Biomol. Chem.
, vol.12
, pp. 3902-3911
-
-
Dughera, S.1
Barbero, M.2
Cadamuro, S.3
Torregrossa, R.4
-
42
-
-
84905748802
-
Towards High-Performance Lewis Acid Organocatalysis
-
Ratjen, L.; van Gemmeren, M.; Pesciaioli, F.; List, B. Towards High-Performance Lewis Acid Organocatalysis Angew. Chem., Int. Ed. 2014, 53, 8765-8769
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 8765-8769
-
-
Ratjen, L.1
Van Gemmeren, M.2
Pesciaioli, F.3
List, B.4
-
43
-
-
16844374787
-
"designer Acids": Combined Acid Catalysis for Asymmetric Synthesis
-
Yamamoto, H.; Futatsugi, K. "Designer Acids": Combined Acid Catalysis for Asymmetric Synthesis Angew. Chem., Int. Ed. 2005, 44, 1924-1942
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 1924-1942
-
-
Yamamoto, H.1
Futatsugi, K.2
-
44
-
-
77954995941
-
Practical Synthetic Approach to Chiral Sulfonimides (CSIs)-Chiral Brønsted Acids for Organocatalysis
-
He, H.; Chen, L.-Y.; Wong, W.-Y.; Chan, W.-H.; Lee, A. W. M. Practical Synthetic Approach to Chiral Sulfonimides (CSIs)-Chiral Brønsted Acids for Organocatalysis Eur. J. Org. Chem. 2010, 4181-4184
-
(2010)
Eur. J. Org. Chem.
, pp. 4181-4184
-
-
He, H.1
Chen, L.-Y.2
Wong, W.-Y.3
Chan, W.-H.4
Lee, A.W.M.5
-
45
-
-
84886415419
-
Synthesis of Optically Pure 3,3′-Diaryl Binaphthyl Disulfonic Acids via Stepwise N-S Bond Cleavage
-
Hatano, M.; Ozaki, T.; Nishikawa, K.; Ishihara, K. Synthesis of Optically Pure 3,3′-Diaryl Binaphthyl Disulfonic Acids via Stepwise N-S Bond Cleavage J. Org. Chem. 2013, 78, 10405-10413
-
(2013)
J. Org. Chem.
, vol.78
, pp. 10405-10413
-
-
Hatano, M.1
Ozaki, T.2
Nishikawa, K.3
Ishihara, K.4
-
46
-
-
84905857890
-
Catalytic Asymmetric Torgov Cyclization: A Concise Total Synthesis of (+)-Estrone
-
Prévost, S.; Dupré, N.; Leutzsch, M.; Wang, Q.; Wakchaure, V.; List, B. Catalytic Asymmetric Torgov Cyclization: A Concise Total Synthesis of (+)-Estrone Angew. Chem., Int. Ed. 2014, 53, 8770-8773
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 8770-8773
-
-
Prévost, S.1
Dupré, N.2
Leutzsch, M.3
Wang, Q.4
Wakchaure, V.5
List, B.6
-
47
-
-
79960043047
-
Synthesis of 3-aryl-4-methyl-1,2-benzenedisulfonimides, new chiral Brønsted acids. A combined experimental and theoretical study
-
Barbero, M.; Bazzi, S.; Cadamuro, S.; Di Bari, L.; Dughera, S.; Ghigo, G.; Padula, D.; Tabasso, S. Synthesis of 3-aryl-4-methyl-1,2-benzenedisulfonimides, new chiral Brønsted acids. A combined experimental and theoretical study Tetrahedron 2011, 67, 5789-5797
-
(2011)
Tetrahedron
, vol.67
, pp. 5789-5797
-
-
Barbero, M.1
Bazzi, S.2
Cadamuro, S.3
Di Bari, L.4
Dughera, S.5
Ghigo, G.6
Padula, D.7
Tabasso, S.8
-
48
-
-
80052184100
-
Chiral Sulfonimide as a Brønsted Acid Organocatalyst for Asymmetric Friedel-Crafts Alkylation of Indoles with Imines
-
Chen, L.-Y.; He, H.; Chan, W.-H.; Lee, A. W. M. Chiral Sulfonimide as a Brønsted Acid Organocatalyst for Asymmetric Friedel-Crafts Alkylation of Indoles with Imines J. Org. Chem. 2011, 76, 7141-7147
-
(2011)
J. Org. Chem.
, vol.76
, pp. 7141-7147
-
-
Chen, L.-Y.1
He, H.2
Chan, W.-H.3
Lee, A.W.M.4
-
49
-
-
0002469154
-
New syntheses of estrone, d,1-8-iso-oestrone and d,1-19-nortestosterone
-
Ananchenko, S. N.; Torgov, I. V. New syntheses of estrone, d,1-8-iso-oestrone and d,1-19-nortestosterone Tetrahedron Lett. 1963, 4, 1553-1558
-
(1963)
Tetrahedron Lett.
, vol.4
, pp. 1553-1558
-
-
Ananchenko, S.N.1
Torgov, I.V.2
-
50
-
-
0026716709
-
An enantioselective version of the AB + B → ABCD-type steroid total synthesis
-
Quinkert, G.; del Grosso, M.; Buchner, A.; Bauch, M.; Döring, W.; Bats, J. W.; Dürner, G. An enantioselective version of the AB + B → ABCD-type steroid total synthesis Tetrahedron Lett. 1992, 33, 3617-3620
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 3617-3620
-
-
Quinkert, G.1
Del Grosso, M.2
Buchner, A.3
Bauch, M.4
Döring, W.5
Bats, J.W.6
Dürner, G.7
-
51
-
-
0006114926
-
A Concise Route to (+)-Estrone
-
Tanaka, K.; Nakashima, H.; Taniguchi, T.; Ogasawara, K. A Concise Route to (+)-Estrone Org. Lett. 2000, 2, 1915-1917
-
(2000)
Org. Lett.
, vol.2
, pp. 1915-1917
-
-
Tanaka, K.1
Nakashima, H.2
Taniguchi, T.3
Ogasawara, K.4
-
52
-
-
33947587428
-
Formal Enantioselective Synthesis of (+)-Estrone
-
Soorukram, D.; Knochel, P. Formal Enantioselective Synthesis of (+)-Estrone Org. Lett. 2007, 9, 1021-1023
-
(2007)
Org. Lett.
, vol.9
, pp. 1021-1023
-
-
Soorukram, D.1
Knochel, P.2
-
53
-
-
34548248667
-
Conversion of Torgovs Synthesis of Estrone into a Highly Enantioselective and Efficient Process
-
Yeung; Chein, R.-J.; Corey, E. J. Conversion of Torgovs Synthesis of Estrone into a Highly Enantioselective and Efficient Process J. Am. Chem. Soc. 2007, 129, 10346-10347
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 10346-10347
-
-
Yeung1
Chein, R.-J.2
Corey, E.J.3
-
54
-
-
49649124668
-
Highly Enantioselective [4 + 2] Cycloaddition Reactions Catalyzed by a Chiral N-Methyl-oxazaborolidinium Cation
-
Canales, E.; Corey, E. J. Highly Enantioselective [4 + 2] Cycloaddition Reactions Catalyzed by a Chiral N-Methyl-oxazaborolidinium Cation Org. Lett. 2008, 10, 3271-3273
-
(2008)
Org. Lett.
, vol.10
, pp. 3271-3273
-
-
Canales, E.1
Corey, E.J.2
-
55
-
-
84898895111
-
Organocatalytic Asymmetric Formation of Steroids
-
Halskov, K. S.; Donslund, B. S.; Barfüsser, S.; Jørgensen, K. A. Organocatalytic Asymmetric Formation of Steroids Angew. Chem., Int. Ed. 2014, 53, 4137-4141
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 4137-4141
-
-
Halskov, K.S.1
Donslund, B.S.2
Barfüsser, S.3
Jørgensen, K.A.4
-
56
-
-
0032493772
-
The first Lewis acid mediated asymmetric Torgov cyclisation
-
Enev, V. S.; Mohr, J.; Harre, M.; Nickisch, K. The first Lewis acid mediated asymmetric Torgov cyclisation Tetrahedron: Asymmetry 1998, 9, 2693-2699
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 2693-2699
-
-
Enev, V.S.1
Mohr, J.2
Harre, M.3
Nickisch, K.4
-
57
-
-
2342556510
-
The Regioisomeric Triphenylaminoethanols-Comparison of Their Efficiency in Enantioselective Catalysis
-
Braun, M.; Fleischer, R.; Mai, B.; Schneider, M.-A.; Lachenicht, S. The Regioisomeric Triphenylaminoethanols-Comparison of Their Efficiency in Enantioselective Catalysis Adv. Synth. Catal. 2004, 346, 474-482
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 474-482
-
-
Braun, M.1
Fleischer, R.2
Mai, B.3
Schneider, M.-A.4
Lachenicht, S.5
-
58
-
-
84918022463
-
Ueber die künstliche Bildung der Milchsäure und einen neuen, dem Glycocoll homologen Körper
-
Strecker, A. Ueber die künstliche Bildung der Milchsäure und einen neuen, dem Glycocoll homologen Körper Justus Liebigs Ann. Chem. 1850, 75, 27-45
-
(1850)
Justus Liebigs Ann. Chem.
, vol.75
, pp. 27-45
-
-
Strecker, A.1
-
59
-
-
0035793657
-
Recent Developments in Catalytic Asymmetric Strecker-Type Reactions
-
Yet, L. Recent Developments in Catalytic Asymmetric Strecker-Type Reactions Angew. Chem., Int. Ed. 2001, 40, 875-877
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 875-877
-
-
Yet, L.1
-
60
-
-
80755152396
-
Asymmetric Strecker Reactions
-
Wang, J.; Liu, X.; Feng, X. Asymmetric Strecker Reactions Chem. Rev. 2011, 111, 6947-6983
-
(2011)
Chem. Rev.
, vol.111
, pp. 6947-6983
-
-
Wang, J.1
Liu, X.2
Feng, X.3
-
61
-
-
0041378065
-
Catalytic Enantioselective Strecker Reactions and Analogous Syntheses
-
Gröger, H. Catalytic Enantioselective Strecker Reactions and Analogous Syntheses Chem. Rev. 2003, 103, 2795-2828
-
(2003)
Chem. Rev.
, vol.103
, pp. 2795-2828
-
-
Gröger, H.1
-
62
-
-
84898937478
-
Kinetics of the Chiral Disulfonimide-Catalyzed Mukaiyama Aldol Reaction
-
Zhang, Z.; List, B. Kinetics of the Chiral Disulfonimide-Catalyzed Mukaiyama Aldol Reaction Asian J. Org. Chem. 2013, 2, 957-960
-
(2013)
Asian J. Org. Chem.
, vol.2
, pp. 957-960
-
-
Zhang, Z.1
List, B.2
-
63
-
-
33746286405
-
Asymmetric Counteranion-Directed Catalysis
-
Mayer, S.; List, B. Asymmetric Counteranion-Directed Catalysis Angew. Chem., Int. Ed. 2006, 45, 4193-4195
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 4193-4195
-
-
Mayer, S.1
List, B.2
-
64
-
-
0025813363
-
Catalytic asymmetric aldol reaction of the silyl enol ether of acetic acid thioester with aldehydes using chiral tin(II) Lewis acid
-
Kobayashi, S.; Furuya, M.; Ohtsubo, A.; Mukaiyama, T. Catalytic asymmetric aldol reaction of the silyl enol ether of acetic acid thioester with aldehydes using chiral tin(II) Lewis acid Tetrahedron: Asymmetry 1991, 2, 635-638
-
(1991)
Tetrahedron: Asymmetry
, vol.2
, pp. 635-638
-
-
Kobayashi, S.1
Furuya, M.2
Ohtsubo, A.3
Mukaiyama, T.4
-
65
-
-
0026525179
-
The catalytic asymmetric aldol reaction of aldehydes with unsubstituted and monosubstituted silyl ketene acetals: Formation of anti-β-hydroxy-α-methyl esters
-
Parmee, E. R.; Hong, Y.; Tempkin, O.; Masamune, S. The catalytic asymmetric aldol reaction of aldehydes with unsubstituted and monosubstituted silyl ketene acetals: Formation of anti-β-hydroxy-α-methyl esters Tetrahedron Lett. 1992, 33, 1729-1732
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 1729-1732
-
-
Parmee, E.R.1
Hong, Y.2
Tempkin, O.3
Masamune, S.4
-
66
-
-
0000376088
-
Catalytic, Enantioselective Aldol Additions with Methyl and Ethyl Acetate O-Silyl Enolates: A Chiral Tridentate Chelate as a Ligand for Titanium(IV)
-
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
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 8837-8838
-
-
Carreira, E.M.1
Singer, R.A.2
Lee, W.3
-
67
-
-
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
-
68
-
-
0028308010
-
Metal versus silyl triflate catalysis in the Mukaiyama aldol addition reaction
-
Carreira, E. M.; Singer, R. A. Metal versus silyl triflate catalysis in the Mukaiyama aldol addition reaction Tetrahedron Lett. 1994, 35, 4323-4326
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 4323-4326
-
-
Carreira, E.M.1
Singer, R.A.2
-
69
-
-
1542520958
-
Homogeneous Catalysis. Mechanisms of the Catalytic Mukaiyama Aldol and Sakurai Allylation Reactions
-
Hollis, T. K.; Bosnich, B. Homogeneous Catalysis. Mechanisms of the Catalytic Mukaiyama Aldol and Sakurai Allylation Reactions J. Am. Chem. Soc. 1995, 117, 4570-4581
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 4570-4581
-
-
Hollis, T.K.1
Bosnich, B.2
-
70
-
-
33646200367
-
Crucial Role of the Conjugate Base for Silyl Lewis Acid Induced Mukaiyama Aldol Reactions
-
Hiraiwa, Y.; Ishihara, K.; Yamamoto, H. Crucial Role of the Conjugate Base for Silyl Lewis Acid Induced Mukaiyama Aldol Reactions Eur. J. Org. Chem. 2006, 1837-1844
-
(2006)
Eur. J. Org. Chem.
, pp. 1837-1844
-
-
Hiraiwa, Y.1
Ishihara, K.2
Yamamoto, H.3
-
71
-
-
0036075713
-
Crucial role of the ligand of silyl Lewis acid in the Mukaiyama aldol reaction
-
Ishihara, K.; Hiraiwa, Y.; Yamamoto, H. Crucial role of the ligand of silyl Lewis acid in the Mukaiyama aldol reaction Chem. Commun. 2002, 1564-1565
-
(2002)
Chem. Commun.
, pp. 1564-1565
-
-
Ishihara, K.1
Hiraiwa, Y.2
Yamamoto, H.3
-
72
-
-
85043003687
-
-
PhD Thesis; Universität zu Köln: Köln, Germany
-
Ratjen, L. PhD Thesis; Universität zu Köln: Köln, Germany, 2012.
-
(2012)
-
-
Ratjen, L.1
-
73
-
-
22744443220
-
Reaction Progress Kinetic Analysis: A Powerful Methodology for Mechanistic Studies of Complex Catalytic Reactions
-
Blackmond, D. G. Reaction Progress Kinetic Analysis: A Powerful Methodology for Mechanistic Studies of Complex Catalytic Reactions Angew. Chem., Int. Ed. 2005, 44, 4302-4320
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4302-4320
-
-
Blackmond, D.G.1
-
74
-
-
0009297190
-
The Principle of Vinylogy
-
Fuson, R. C. The Principle of Vinylogy Chem. Rev. 1935, 16, 1-27
-
(1935)
Chem. Rev.
, vol.16
, pp. 1-27
-
-
Fuson, R.C.1
-
75
-
-
0343248968
-
The Application of the Principle of Vinylogy to Unsaturated Ketones
-
Christ, R. E.; Fuson, R. C. The Application of the Principle of Vinylogy to Unsaturated Ketones J. Am. Chem. Soc. 1937, 59, 893-897
-
(1937)
J. Am. Chem. Soc.
, vol.59
, pp. 893-897
-
-
Christ, R.E.1
Fuson, R.C.2
-
76
-
-
78651383697
-
Disulfonimide-Catalyzed Asymmetric Vinylogous and Bisvinylogous Mukaiyama Aldol Reactions
-
Ratjen, L.; García-García, P.; Lay, F.; Beck, M. E.; List, B. Disulfonimide-Catalyzed Asymmetric Vinylogous and Bisvinylogous Mukaiyama Aldol Reactions Angew. Chem., Int. Ed. 2011, 50, 754-758
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 754-758
-
-
Ratjen, L.1
García-García, P.2
Lay, F.3
Beck, M.E.4
List, B.5
-
77
-
-
0001151356
-
Catalytic, Enantioselective Dienolate Additions to Aldehydes: Preparation of Optically Active Acetoacetate Aldol Adducts
-
Singer, R. A.; Carreira, E. M. Catalytic, Enantioselective Dienolate Additions to Aldehydes: Preparation of Optically Active Acetoacetate Aldol Adducts J. Am. Chem. Soc. 1995, 117, 12360-12361
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 12360-12361
-
-
Singer, R.A.1
Carreira, E.M.2
-
78
-
-
0038475549
-
Apparent Catalytic Generation of Chiral Metal Enolates: Enantioselective Dienolate Additions to Aldehydes Mediated by Tol-BINAP·Cu(II) Fluoride Complexes
-
Krüger, J.; Carreira, E. M. Apparent Catalytic Generation of Chiral Metal Enolates: Enantioselective Dienolate Additions to Aldehydes Mediated by Tol-BINAP·Cu(II) Fluoride Complexes J. Am. Chem. Soc. 1998, 120, 837-838
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 837-838
-
-
Krüger, J.1
Carreira, E.M.2
-
79
-
-
0035847523
-
Vinylogous Mukaiyama aldol reactions with triarylboranes
-
Christmann, M.; Kalesse, M. Vinylogous Mukaiyama aldol reactions with triarylboranes Tetrahedron Lett. 2001, 42, 1269-1271
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 1269-1271
-
-
Christmann, M.1
Kalesse, M.2
-
80
-
-
0346162171
-
Highly Enantioselective Cr(salen)-catalyzed Reaction of 2-(Trimethylsilyloxy)furan and Aldehydes. Effect of Alcohol on Enantioselectivity
-
Onitsuka, S.; Matsuoka, Y.; Irie, R.; Katsuki, T. Highly Enantioselective Cr(salen)-catalyzed Reaction of 2-(Trimethylsilyloxy)furan and Aldehydes. Effect of Alcohol on Enantioselectivity Chem. Lett. 2003, 32, 974-975
-
(2003)
Chem. Lett.
, vol.32
, pp. 974-975
-
-
Onitsuka, S.1
Matsuoka, Y.2
Irie, R.3
Katsuki, T.4
-
81
-
-
30744451484
-
Recent Advances in Vinylogous Aldol Reactions and Their Applications in the Syntheses of Natural Products
-
Mulzer, J. Springer: Berlin/Heidelberg, Germany
-
Kalesse, M. Recent Advances in Vinylogous Aldol Reactions and Their Applications in the Syntheses of Natural Products. In Natural Products Synthesis II; Mulzer, J., Ed.; Springer: Berlin/Heidelberg, Germany, 2005; Vol. 244, pp 43-76.
-
(2005)
Natural Products Synthesis II
, vol.244
, pp. 43-76
-
-
Kalesse, M.1
-
82
-
-
62349099126
-
Highly Stereoselective Aldol Reactions in the Total Syntheses of Complex Natural Products
-
Brodmann, T.; Lorenz, M.; Schäckel, R.; Simsek, S.; Kalesse, M. Highly Stereoselective Aldol Reactions in the Total Syntheses of Complex Natural Products Synlett 2009, 174-192
-
(2009)
Synlett
, pp. 174-192
-
-
Brodmann, T.1
Lorenz, M.2
Schäckel, R.3
Simsek, S.4
Kalesse, M.5
-
83
-
-
77952703010
-
Organocatalyzed Highly Enantioselective and anti-Selective Construction of γ-Butenolides through Vinylogous Mukaiyama Aldol Reaction
-
Zhu, N.; Ma, B.-C.; Zhang, Y.; Wang, W. Organocatalyzed Highly Enantioselective and anti-Selective Construction of γ-Butenolides through Vinylogous Mukaiyama Aldol Reaction Adv. Synth. Catal. 2010, 352, 1291-1295
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1291-1295
-
-
Zhu, N.1
Ma, B.-C.2
Zhang, Y.3
Wang, W.4
-
84
-
-
84865428726
-
Highly Enantioselective Hetero-Diels-Alder Reaction of 1,3-Bis(silyloxy)-1,3-dienes with Aldehydes Catalyzed by Chiral Disulfonimide
-
Guin, J.; Rabalakos, C.; List, B. Highly Enantioselective Hetero-Diels-Alder Reaction of 1,3-Bis(silyloxy)-1,3-dienes with Aldehydes Catalyzed by Chiral Disulfonimide Angew. Chem., Int. Ed. 2012, 51, 8859-8863
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 8859-8863
-
-
Guin, J.1
Rabalakos, C.2
List, B.3
-
85
-
-
33847805195
-
Useful diene for the Diels-Alder reaction
-
Danishefsky, S.; Kitahara, T. Useful diene for the Diels-Alder reaction J. Am. Chem. Soc. 1974, 96, 7807-7808
-
(1974)
J. Am. Chem. Soc.
, vol.96
, pp. 7807-7808
-
-
Danishefsky, S.1
Kitahara, T.2
-
86
-
-
0000570755
-
Lewis acid catalyzed cyclocondensations of functionalized dienes with aldehydes
-
Danishefsky, S.; Kerwin, J. F.; Kobayashi, S. Lewis acid catalyzed cyclocondensations of functionalized dienes with aldehydes J. Am. Chem. Soc. 1982, 104, 358-360
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 358-360
-
-
Danishefsky, S.1
Kerwin, J.F.2
Kobayashi, S.3
-
87
-
-
26844544456
-
Biocatalytic Approaches to Hetero-Diels-Alder Adducts of Carbonyl Compounds
-
Gouverneur, V.; Reiter, M. Biocatalytic Approaches to Hetero-Diels-Alder Adducts of Carbonyl Compounds Chem.-Eur. J. 2005, 11, 5806-5815
-
(2005)
Chem.-Eur. J.
, vol.11
, pp. 5806-5815
-
-
Gouverneur, V.1
Reiter, M.2
-
88
-
-
61849131140
-
Asymmetric hetero-Diels-Alder reactions of carbonyl compounds
-
Pellissier, H. Asymmetric hetero-Diels-Alder reactions of carbonyl compounds Tetrahedron 2009, 65, 2839-2877
-
(2009)
Tetrahedron
, vol.65
, pp. 2839-2877
-
-
Pellissier, H.1
-
89
-
-
84907820575
-
The Asymmetric Hetero-Diels-Alder Reaction in the Syntheses of Biologically Relevant Compounds
-
Eschenbrenner-Lux, V.; Kumar, K.; Waldmann, H. The Asymmetric Hetero-Diels-Alder Reaction in the Syntheses of Biologically Relevant Compounds Angew. Chem., Int. Ed. 2014, 53, 11146-11157
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 11146-11157
-
-
Eschenbrenner-Lux, V.1
Kumar, K.2
Waldmann, H.3
-
90
-
-
0000146865
-
Asymmetric hetero Diels-Alder reactions catalyzed by novel chiral vanadium(IV) bis(1,3-diketonato) complexes
-
Togni, A. Asymmetric hetero Diels-Alder reactions catalyzed by novel chiral vanadium(IV) bis(1,3-diketonato) complexes Organometallics 1990, 9, 3106-3113
-
(1990)
Organometallics
, vol.9
, pp. 3106-3113
-
-
Togni, A.1
-
91
-
-
0027269527
-
Stereocontrolled Syntheses of Polysubstituted 2,3-Dihydro-4H-pyran-4-ones by Cyclocondensation of β-Acyloxy-ketones
-
Oppolzer, W.; Rodriguez, I. Stereocontrolled Syntheses of Polysubstituted 2,3-Dihydro-4H-pyran-4-ones by Cyclocondensation of β-Acyloxy-ketones Helv. Chim. Acta 1993, 76, 1282-1291
-
(1993)
Helv. Chim. Acta
, vol.76
, pp. 1282-1291
-
-
Oppolzer, W.1
Rodriguez, I.2
-
92
-
-
13444311672
-
A Catalytic Asymmetric Bioorganic Route to Enantioenriched Tetrahydro- and Dihydropyranones
-
Baker-Glenn, C.; Hodnett, N.; Reiter, M.; Ropp, S.; Ancliff, R.; Gouverneur, V. A Catalytic Asymmetric Bioorganic Route to Enantioenriched Tetrahydro- and Dihydropyranones J. Am. Chem. Soc. 2005, 127, 1481-1486
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 1481-1486
-
-
Baker-Glenn, C.1
Hodnett, N.2
Reiter, M.3
Ropp, S.4
Ancliff, R.5
Gouverneur, V.6
-
93
-
-
26844452226
-
Highly Enantioselective Synthesis of 2,6-Disubstituted and 2,2,6-Trisubstituted Dihydropyrones: A One-Step Synthesis of (R)-(+)-Hepialone and Its Analogues
-
Yang, W.; Shang, D.; Liu, Y.; Du, Y.; Feng, X. Highly Enantioselective Synthesis of 2,6-Disubstituted and 2,2,6-Trisubstituted Dihydropyrones: A One-Step Synthesis of (R)-(+)-Hepialone and Its Analogues J. Org. Chem. 2005, 70, 8533-8537
-
(2005)
J. Org. Chem.
, vol.70
, pp. 8533-8537
-
-
Yang, W.1
Shang, D.2
Liu, Y.3
Du, Y.4
Feng, X.5
-
94
-
-
38849089406
-
New 7,8-benzoflavanones as potent aromatase inhibitors: Synthesis and biological evaluation
-
Yahiaoui, S.; Fagnere, C.; Pouget, C.; Buxeraud, J.; Chulia, A.-J. New 7,8-benzoflavanones as potent aromatase inhibitors: Synthesis and biological evaluation Bioorg. Med. Chem. 2008, 16, 1474-1480
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 1474-1480
-
-
Yahiaoui, S.1
Fagnere, C.2
Pouget, C.3
Buxeraud, J.4
Chulia, A.-J.5
-
95
-
-
79955618401
-
Lead optimization of 4-imidazolylflavans: New promising aromatase inhibitors
-
Yahiaoui, S.; Pouget, C.; Buxeraud, J.; Chulia, A. J.; Fagnère, C. Lead optimization of 4-imidazolylflavans: New promising aromatase inhibitors Eur. J. Med. Chem. 2011, 46, 2541-2545
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 2541-2545
-
-
Yahiaoui, S.1
Pouget, C.2
Buxeraud, J.3
Chulia, A.J.4
Fagnère, C.5
-
96
-
-
0032557195
-
Determination of the Nucleophilicities of Silyl and Alkyl Enol Ethers
-
Burfeindt, J.; Patz, M.; Müller, M.; Mayr, H. Determination of the Nucleophilicities of Silyl and Alkyl Enol Ethers J. Am. Chem. Soc. 1998, 120, 3629-3634
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 3629-3634
-
-
Burfeindt, J.1
Patz, M.2
Müller, M.3
Mayr, H.4
-
97
-
-
84857552255
-
Low-loading asymmetric organocatalysis
-
Giacalone, F.; Gruttadauria, M.; Agrigento, P.; Noto, R. Low-loading asymmetric organocatalysis Chem. Soc. Rev. 2012, 41, 2406-2447
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 2406-2447
-
-
Giacalone, F.1
Gruttadauria, M.2
Agrigento, P.3
Noto, R.4
-
99
-
-
37349005457
-
Organocatalytic Asymmetric Mannich Reactions: New Methodology, Catalyst Design, and Synthetic Applications
-
Ting, A.; Schaus, S. E. Organocatalytic Asymmetric Mannich Reactions: New Methodology, Catalyst Design, and Synthetic Applications Eur. J. Org. Chem. 2007, 2007, 5797-5815
-
(2007)
Eur. J. Org. Chem.
, vol.2007
, pp. 5797-5815
-
-
Ting, A.1
Schaus, S.E.2
-
100
-
-
38149118178
-
Organocatalysed asymmetric Mannich reactions
-
Verkade, J. M. M.; Hemert, L. J. C. v.; Quaedflieg, P. J. L. M.; Rutjes, F. P. J. T. Organocatalysed asymmetric Mannich reactions Chem. Soc. Rev. 2008, 37, 29-41
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 29-41
-
-
Verkade, J.M.M.1
Hemert, L.J.C.V.2
Quaedflieg, P.J.L.M.3
Rutjes, F.P.J.T.4
-
101
-
-
84886875117
-
Disulfonimide-Catalyzed Asymmetric Synthesis of β3-Amino Esters Directly from N-Boc-Amino Sulfones
-
Wang, Q.; Leutzsch, M.; van Gemmeren, M.; List, B. Disulfonimide-Catalyzed Asymmetric Synthesis of β3-Amino Esters Directly from N-Boc-Amino Sulfones J. Am. Chem. Soc. 2013, 135, 15334-15337
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 15334-15337
-
-
Wang, Q.1
Leutzsch, M.2
Van Gemmeren, M.3
List, B.4
-
102
-
-
0346732156
-
The First Catalytic Highly Enantioselective Alkylation of Ketimines-A Novel Approach to Optically Active Quaternary α-Amino Acids
-
Saaby, S.; Nakama, K.; Lie, M. A.; Hazell, R. G.; Jørgensen, K. A. The First Catalytic Highly Enantioselective Alkylation of Ketimines-A Novel Approach to Optically Active Quaternary α-Amino Acids Chem.-Eur. J. 2003, 9, 6145-6154
-
(2003)
Chem.-Eur. J.
, vol.9
, pp. 6145-6154
-
-
Saaby, S.1
Nakama, K.2
Lie, M.A.3
Hazell, R.G.4
Jørgensen, K.A.5
-
103
-
-
84891583943
-
-
Wiley-VCH: Weinheim, Germany
-
Schneider, C.; Sickert, M. Chiral Amine Synthesis-Methods, Developments and Applications; Wiley-VCH: Weinheim, Germany, 2010; p 523.
-
(2010)
Chiral Amine Synthesis-Methods, Developments and Applications
, pp. 523
-
-
Schneider, C.1
Sickert, M.2
-
104
-
-
84915766639
-
Asymmetric Disulfonimide-Catalyzed Synthesis of -Amino-β-Ketoester Derivatives by Vinylogous Mukaiyama-Mannich Reactions
-
Wang, Q.; van Gemmeren, M.; List, B. Asymmetric Disulfonimide-Catalyzed Synthesis of -Amino-β-Ketoester Derivatives by Vinylogous Mukaiyama-Mannich Reactions Angew. Chem., Int. Ed. 2014, 53, 13592-13595
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 13592-13595
-
-
Wang, Q.1
Van Gemmeren, M.2
List, B.3
-
105
-
-
49549128832
-
Syntheses of γ,-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride
-
Hosomi, A.; Sakurai, H. Syntheses of γ,-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride Tetrahedron Lett. 1976, 17, 1295-1298
-
(1976)
Tetrahedron Lett.
, vol.17
, pp. 1295-1298
-
-
Hosomi, A.1
Sakurai, H.2
-
107
-
-
85022536996
-
Chiral (Acyloxy)borane Catalyzed Asymmetric Allylation of Aldehydes
-
Furuta, K.; Mouri, M.; Yamamoto, H. Chiral (Acyloxy)borane Catalyzed Asymmetric Allylation of Aldehydes Synlett 1991, 561-562
-
(1991)
Synlett
, pp. 561-562
-
-
Furuta, K.1
Mouri, M.2
Yamamoto, H.3
-
108
-
-
0000008279
-
Catalytic asymmetric allylation using a chiral (acyloxy)borane complex as a versatile Lewis acid catalyst
-
Ishihara, K.; Mouri, M.; Gao, Q.; Maruyama, T.; Furuta, K.; Yamamoto, H. Catalytic asymmetric allylation using a chiral (acyloxy)borane complex as a versatile Lewis acid catalyst J. Am. Chem. Soc. 1993, 115, 11490-11495
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 11490-11495
-
-
Ishihara, K.1
Mouri, M.2
Gao, Q.3
Maruyama, T.4
Furuta, K.5
Yamamoto, H.6
-
109
-
-
84870928356
-
Asymmetric Counteranion-Directed Catalytic Hosomi-Sakurai Reaction
-
Mahlau, M.; García-García, P.; List, B. Asymmetric Counteranion-Directed Catalytic Hosomi-Sakurai Reaction Chem.-Eur. J. 2012, 18, 16283-16287
-
(2012)
Chem.-Eur. J.
, vol.18
, pp. 16283-16287
-
-
Mahlau, M.1
García-García, P.2
List, B.3
-
110
-
-
33846906752
-
Recent developments in asymmetric catalytic addition to C-N bonds
-
Friestad, G. K.; Mathies, A. K. Recent developments in asymmetric catalytic addition to C-N bonds Tetrahedron 2007, 63, 2541-2569
-
(2007)
Tetrahedron
, vol.63
, pp. 2541-2569
-
-
Friestad, G.K.1
Mathies, A.K.2
-
111
-
-
79954999802
-
Allylation of Imines and Their Derivatives with Organoboron Reagents: Stereocontrolled Synthesis of Homoallylic Amines
-
Ramadhar, T. R.; Batey, R. A. Allylation of Imines and Their Derivatives with Organoboron Reagents: Stereocontrolled Synthesis of Homoallylic Amines Synthesis 2011, 9, 1321-1346
-
(2011)
Synthesis
, vol.9
, pp. 1321-1346
-
-
Ramadhar, T.R.1
Batey, R.A.2
-
112
-
-
83755178261
-
Catalytic Enantioselective Allylation of Carbonyl Compounds and Imines
-
Yus, M.; González-Gómez, J. C.; Foubelo, F. Catalytic Enantioselective Allylation of Carbonyl Compounds and Imines Chem. Rev. 2011, 111, 7774-7854
-
(2011)
Chem. Rev.
, vol.111
, pp. 7774-7854
-
-
Yus, M.1
González-Gómez, J.C.2
Foubelo, F.3
-
113
-
-
84874243120
-
Catalytic Asymmetric Three-Component Synthesis of Homoallylic Amines
-
Gandhi, S.; List, B. Catalytic Asymmetric Three-Component Synthesis of Homoallylic Amines Angew. Chem., Int. Ed. 2013, 52, 2573-2576
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 2573-2576
-
-
Gandhi, S.1
List, B.2
-
114
-
-
0037201534
-
Recent advances in the stereoselective synthesis of β-amino acids
-
Liu, M.; Sibi, M. P. Recent advances in the stereoselective synthesis of β-amino acids Tetrahedron 2002, 58, 7991-8035
-
(2002)
Tetrahedron
, vol.58
, pp. 7991-8035
-
-
Liu, M.1
Sibi, M.P.2
-
115
-
-
49249117085
-
Catalytic Enantioselective Hydrophosphonylation of Aldehydes and Imines
-
Merino, P.; Marqués-López, E.; Herrera, R. P. Catalytic Enantioselective Hydrophosphonylation of Aldehydes and Imines Adv. Synth. Catal. 2008, 350, 1195-1208
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1195-1208
-
-
Merino, P.1
Marqués-López, E.2
Herrera, R.P.3
-
116
-
-
84863229367
-
Recent developments in metal catalyzed asymmetric addition of phosphorus nucleophiles
-
Zhao, D.; Wang, R. Recent developments in metal catalyzed asymmetric addition of phosphorus nucleophiles Chem. Soc. Rev. 2012, 41, 2095-2108
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 2095-2108
-
-
Zhao, D.1
Wang, R.2
-
117
-
-
0036851640
-
How to Get the Most out of Two Phosphorus Chemistries. Studies on H-Phosphonates
-
Stawinski, J.; Kraszewski, A. How To Get the Most Out of Two Phosphorus Chemistries. Studies on H-Phosphonates Acc. Chem. Res. 2002, 35, 952-260
-
(2002)
Acc. Chem. Res.
, vol.35
, pp. 952-260
-
-
Stawinski, J.1
Kraszewski, A.2
-
118
-
-
0001645060
-
Reaction of dialkyl phosphites with aldehydes and ketones (a new method of synthesis of esters of hydroxyalkanephosphonic acids)
-
Abramov, V. S. Reaction of dialkyl phosphites with aldehydes and ketones (a new method of synthesis of esters of hydroxyalkanephosphonic acids) Dokl. Akad. Nauk SSSR 1950, 73, 487-489
-
(1950)
Dokl. Akad. Nauk SSSR
, vol.73
, pp. 487-489
-
-
Abramov, V.S.1
-
119
-
-
0001288911
-
Reaction of aldehydes with phosphites
-
Abramov, V. S. Reaction of aldehydes with phosphites Dokl. Akad. Nauk SSSR 1954, 95, 991-992
-
(1954)
Dokl. Akad. Nauk SSSR
, vol.95
, pp. 991-992
-
-
Abramov, V.S.1
-
120
-
-
0000418047
-
Silyl esters of phosphorous-Common intermediates in synthesis
-
Woźniak, L.; Chojnowski, J. Silyl esters of phosphorous-Common intermediates in synthesis Tetrahedron 1989, 45, 2465-2524
-
(1989)
Tetrahedron
, vol.45
, pp. 2465-2524
-
-
Woźniak, L.1
Chojnowski, J.2
-
121
-
-
84920153803
-
The Catalytic Asymmetric Abramov Reaction
-
Guin, J.; Wang, Q.; van Gemmeren, M.; List, B. The Catalytic Asymmetric Abramov Reaction Angew. Chem., Int. Ed. 2015, 54, 355-358
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 355-358
-
-
Guin, J.1
Wang, Q.2
Van Gemmeren, M.3
List, B.4
-
122
-
-
78349296042
-
Metal Triflimidates: Better than Metal Triflates as Catalysts in Organic Synthesis-The Effect of a Highly Delocalized Counteranion
-
Antoniotti, S.; Dalla, V.; Duñach, E. Metal Triflimidates: Better than Metal Triflates as Catalysts in Organic Synthesis-The Effect of a Highly Delocalized Counteranion Angew. Chem., Int. Ed. 2010, 49, 7860-7888
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 7860-7888
-
-
Antoniotti, S.1
Dalla, V.2
Duñach, E.3
|