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Volumn 115, Issue 17, 2015, Pages 9388-9409

Development and Applications of Disulfonimides in Enantioselective Organocatalysis

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOSELECTIVITY; TRANSITION METALS;

EID: 84941032548     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/acs.chemrev.5b00128     Document Type: Review
Times cited : (253)

References (122)
  • 1
    • 2342570203 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 12
    • 84871951289 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 21
    • 77956485890 scopus 로고    scopus 로고
    • 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
  • 23
    • 84886007342 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 34
    • 84872002336 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • PhD Thesis; Universität zu Köln, Köln, Germany
    • Hoffmann, S. PhD Thesis; Universität zu Köln, Köln, Germany, 2008.
    • (2008)
    • Hoffmann, S.1
  • 40
    • 84860783753 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 43
    • 16844374787 scopus 로고    scopus 로고
    • "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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 47
    • 79960043047 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 52
    • 33947587428 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 56
    • 0032493772 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 68
    • 0028308010 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • PhD Thesis; Universität zu Köln: Köln, Germany
    • Ratjen, L. PhD Thesis; Universität zu Köln: Köln, Germany, 2012.
    • (2012)
    • Ratjen, L.1
  • 73
    • 22744443220 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 99
    • 37349005457 scopus 로고    scopus 로고
    • 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
  • 101
    • 84886875117 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 104
    • 84915766639 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 122
    • 78349296042 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.