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Volumn 85, Issue 8, 2009, Pages 290-313

Rational design of dynamic ammonium salt catalysts towards more flexible and selective function

Author keywords

2+2 cycloaddition reaction; Acid base combinsation chemistry; Dehydrative condensation; Diels Alder reaction; Dynamic salt complex; Mannich type reaction

Indexed keywords

ALNUS;

EID: 74949085498     PISSN: 03862208     EISSN: 13492896     Source Type: Journal    
DOI: 10.2183/pjab.85.290     Document Type: Review
Times cited : (27)

References (74)
  • 2
    • 33947728159 scopus 로고    scopus 로고
    • Design of highly functional small-molecule catalysts and related reactions based on acid-base combination chemistry
    • Ishihara, K., Sakakura, A. and Hatano, M. (2007) Design of highly functional small-molecule catalysts and related reactions based on acid-base combination chemistry. Synlett, no. 5, 686-703.
    • (2007) Synlett , vol.0 , Issue.5 , pp. 686-703
    • Ishihara, K.1    Sakakura, A.2    Hatano, M.3
  • 3
    • 58149183749 scopus 로고    scopus 로고
    • Dehydrative condensation catalyses
    • Ishihara, K. (2009) Dehydrative condensation catalyses. Tetrahedron 65, 1085-1109.
    • (2009) Tetrahedron , vol.65 , pp. 1085-1109
    • Ishihara, K.1
  • 4
    • 0034234818 scopus 로고    scopus 로고
    • Diphenylammonium triflate (DPAT): Efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols
    • Wakasugi, K., Misaki, T., Yamada, K. and Tanabe, Y. (2000) Diphenylammonium triflate (DPAT): Efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols. Tetrahedron Lett. 41, 5249-5252.
    • (2000) Tetrahedron Lett , vol.41 , pp. 5249-5252
    • Wakasugi, K.1    Misaki, T.2    Yamada, K.3    Tanabe, Y.4
  • 5
    • 33751359795 scopus 로고    scopus 로고
    • Pentafluorophenylammonium Triflate (PFPAT): An efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation
    • Funatomi, T., Wakasugi, K., Misaki, T. and Tanabe, Y. (2006) Pentafluorophenylammonium Triflate (PFPAT): An efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation. Green Chem. 8, 1022-1027.
    • (2006) Green Chem , vol.8 , pp. 1022-1027
    • Funatomi, T.1    Wakasugi, K.2    Misaki, T.3    Tanabe, Y.4
  • 6
    • 0034634399 scopus 로고    scopus 로고
    • Direct condensation of carboxylic acids with alcohols catalyzed by hafnium(IV) salts
    • Ishihara, K., Ohara, S. and Yamamoto, H. (2000) Direct condensation of carboxylic acids with alcohols catalyzed by hafnium(IV) salts. Science 290, 1140-1142.
    • (2000) Science , vol.290 , pp. 1140-1142
    • Ishihara, K.1    Ohara, S.2    Yamamoto, H.3
  • 7
    • 0034930214 scopus 로고    scopus 로고
    • A green method for the selective esterification of primary alcohols in the presence of secondary alcohols or aromatic alcohols
    • Ishihara, K., Nakayama, M., Ohara, S. and Yamamoto, H. (2001) A green method for the selective esterification of primary alcohols in the presence of secondary alcohols or aromatic alcohols. Synlett 7, 1117-1120.
    • (2001) Synlett , vol.7 , pp. 1117-1120
    • Ishihara, K.1    Nakayama, M.2    Ohara S3    Yamamoto, H.4
  • 8
    • 0037037934 scopus 로고    scopus 로고
    • Direct ester condensation from a 1:1 mixture of carboxylic acids and alcohols catalyzed by hafnium(IV) or zirconium(IV) salts
    • Ishihara, K., Nakayama, M., Ohara, S. and Yamamoto, H. (2002) Direct ester condensation from a 1:1 mixture of carboxylic acids and alcohols catalyzed by hafnium(IV) or zirconium(IV) salts. Tetrahedron 58, 8179-8188.
    • (2002) Tetrahedron , vol.58 , pp. 8179-8188
    • Ishihara, K.1    Nakayama, M.2    Ohara S3    Yamamoto, H.4
  • 9
    • 7044239414 scopus 로고    scopus 로고
    • Water-tolerant and reusable catalysts for direct ester condensation between equimolar amounts of carboxylic acids and alcohols
    • Nakayama, M., Sato, A., Ishihara, K and Yamamoto, H. (2004) Water-tolerant and reusable catalysts for direct ester condensation between equimolar amounts of carboxylic acids and alcohols. Adv. Synth. Catal. 346, 1275-1279.
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1275-1279
    • Nakayama, M.1    Sato, A.2    Ishihara, K.3    Yamamoto, H.4
  • 10
    • 24644458677 scopus 로고    scopus 로고
    • Zr(IV)-Fe(III), -Ga(III), and -SN(IV) binary metal complexes as synergistic and reusable esterification catalysts
    • Sato, A., Nakamura, Y., Maki, T., Ishihara, K. and Yamamoto, H. (2005) Zr(IV)-Fe(III), -Ga(III), and -SN(IV) binary metal complexes as synergistic and reusable esterification catalysts. Adv. Synth. Catal. 347, 1337-1340.
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 1337-1340
    • Sato, A.1    Nakamura, Y.2    Maki, T.3    Ishihara, K.4    Yamamoto, H.5
  • 11
    • 33748270464 scopus 로고    scopus 로고
    • Iron(III)-zirconium(IV) combines salt immobilized on N-(polystylylbutyl)pyridinium triflylimide as a reusable catalyst for a dehydrative esterification reaction
    • Nakamura, Y., Maki, T., Wang, X., Ishihara, K. and Yamamoto, H. (2006) Iron(III)-zirconium(IV) combines salt immobilized on N-(polystylylbutyl) pyridinium triflylimide as a reusable catalyst for a dehydrative esterification reaction. Adv. Synth. Catal. 348, 1505-1510.
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 1505-1510
    • Nakamura, Y.1    Maki, T.2    Wang, X.3    Ishihara, K.4    Yamamoto, H.5
  • 12
    • 16244400119 scopus 로고    scopus 로고
    • Bulky diarylammonium arenesulfonates as selective esterification catalysts
    • Ishihara, K., Nakagawa, S. and Sakakura, A. (2005) Bulky diarylammonium arenesulfonates as selective esterification catalysts. J. Am. Chem. Soc. 127, 4168-4169.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 4168-4169
    • Ishihara, K.1    Nakagawa, S.2    Sakakura, A.3
  • 13
    • 28944444304 scopus 로고    scopus 로고
    • Bulky diarlammonium arenesulfonates as mild and extremely active dehydrative ester condensation catalysts
    • Sakakura, A., Nakagawa, S. and Ishihara, K. (2006) Bulky diarlammonium arenesulfonates as mild and extremely active dehydrative ester condensation catalysts. Tetrahedron 62, 422-433.
    • (2006) Tetrahedron , vol.62 , pp. 422-433
    • Sakakura, A.1    Nakagawa, S.2    Ishihara, K.3
  • 14
    • 34548581078 scopus 로고    scopus 로고
    • Direct ester condensation catalyzed by bulky diarylammonium pentafluorobenzenesulfonates
    • Sakakura, A., Nakagawa, S. and Ishihara, K. (2007) Direct ester condensation catalyzed by bulky diarylammonium pentafluorobenzenesulfonates. Nature Protocols 2, 1746-1751.
    • (2007) Nature Protocols , vol.2 , pp. 1746-1751
    • Sakakura, A.1    Nakagawa, S.2    Ishihara, K.3
  • 15
    • 46749125277 scopus 로고    scopus 로고
    • Open-air and solvent-free ester condensation catalyzed by sulfonic acids
    • Sakakura, A., Koshikari, Y. and Ishihara, K. (2008) Open-air and solvent-free ester condensation catalyzed by sulfonic acids. Tetrahedron Lett. 49, 5017-5020.
    • (2008) Tetrahedron Lett , vol.49 , pp. 5017-5020
    • Sakakura, A.1    Koshikari, Y.2    Ishihara, K.3
  • 16
    • 34250794551 scopus 로고    scopus 로고
    • Unusual rate acceleration in Brønsted acid catalyzed dehydration reactions: Local hydrophobic environment in aggregated N-(2 6-diphenylphenyl)-N-mesitylammonium pentafluorobenzenesulfonates
    • Sakakura, A., Watanabe, H., Nakagawa, S. and Ishihara, K. (2007) Unusual rate acceleration in Brønsted acid catalyzed dehydration reactions: Local hydrophobic environment in aggregated N-(2,6-diphenylphenyl)-N-mesitylammonium pentafluorobenzenesulfonates. Chem. Asian J. 2, 477-483.
    • (2007) Chem. Asian J. , vol.2 , pp. 477-483
    • Sakakura, A.1    Watanabe, H.2    Nakagawa, S.3    Ishihara, K.4
  • 17
    • 0037429060 scopus 로고    scopus 로고
    • Esterification of sterically hindered acids and alcohols in fluorous media
    • Gacem, B. and Jenner, G. (2003) Esterification of sterically hindered acids and alcohols in fluorous media. Tetrahedron Lett. 44, 1391-1393.
    • (2003) Tetrahedron Lett , vol.44 , pp. 1391-1393
    • Gacem, B.1    Jenner, G.2
  • 19
    • 0010066824 scopus 로고
    • Determination of dissociation constants of acids in glacial acetic acid by proton magnetic resonance
    • Rode, B. M., Engelbrechit, A. and Schantl, J. (1973) Determination of dissociation constants of acids in glacial acetic acid by proton magnetic resonance. Z. Physik. Chem. (Leipzig) 253, 17-24.
    • (1973) Z. Physik. Chem. (Leipzig) , vol.253 , pp. 17-24
    • Rode, B.M.1    Engelbrechit, A.2    Schantl, J.3
  • 20
    • 16244389408 scopus 로고
    • o von pentafluorbenzenzolsulfonsxure und petafluorbenzoesxure in aceton
    • o von pentafluorbenzenzolsulfonsxure und petafluorbenzoesxure in aceton. J. Fluorine Chem. 20, 559-572.
    • (1982) J. Fluorine Chem. , vol.20 , pp. 559-572
    • Habel, W.1    Sartori, P.2
  • 21
    • 47749122232 scopus 로고    scopus 로고
    • Berkessel, H. and Gröger, H. (eds.) Wiley-VCH, Weinheim
    • Berkessel, H. and Gröger, H. (eds.) (2005) Asymmetric Organocatalysis. Wiley-VCH, Weinheim.
    • (2005) Asymmetric Organocatalysis
  • 22
    • 38349189109 scopus 로고    scopus 로고
    • Stronger Brønsted acids
    • Akiyama, T. (2007) Stronger Brønsted acids. Chem. Rev. 107, 5744-5758.
    • (2007) Chem. Rev. , vol.107 , pp. 5744-5758
    • Akiyama, T.1
  • 23
    • 0141923582 scopus 로고    scopus 로고
    • Asymmetric Morita-Baylis-Hillman reactions catalyzed by chiral Brønsted acids
    • McDougal, N. T. and Schaus, S. E. (2003) Asymmetric Morita-Baylis-Hillman reactions catalyzed by chiral Brønsted acids. J. Am. Chem. Soc. 125, 12094-12095.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 12094-12095
    • McDougal, N.T.1    Schaus, S.E.2
  • 24
    • 2342570203 scopus 로고    scopus 로고
    • Enantioselective Mannich-type reaction catalyzed by a chiral Brønsted acid
    • Akiyama, T., Itoh, J., Yokota, K. and Fuchibe, K. (2004) Enantioselective Mannich-type reaction catalyzed by a chiral Brønsted acid. Angew. Chem., Int. Ed. 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
  • 25
    • 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. and Yamamoto, H. (2006) Design of chiral N-triflyl phosphoramide as a strong chiral Brønsted acid and its application to asymmetric Diels-Alder reaction. J. Am. Chem. Soc. 128, 9626-9627.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9626-9627
    • Nakashima, D.1    Yamamoto, H.2
  • 26
    • 34548191726 scopus 로고    scopus 로고
    • Design of axially chiral dicarboxylic acid for asymmetric Mannich reaction of arylaldehyde N-Boc imines and diazo compounds
    • Hashimoto, T. and Maruoka, K. (2007) Design of axially chiral dicarboxylic acid for asymmetric Mannich reaction of arylaldehyde N-Boc imines and diazo compounds. J. Am. Chem. Soc. 129, 10054-10055.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 10054-10055
    • Hashimoto, T.1    Maruoka, K.2
  • 27
    • 2342521907 scopus 로고    scopus 로고
    • Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation
    • Uraguchi, D. and Terada, M. (2004) Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation. J. Am. Chem. Soc. 126, 5356-5357.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5356-5357
    • Uraguchi, D.1    Terada, M.2
  • 28
    • 30544448390 scopus 로고    scopus 로고
    • Phosphorodiamidic acid as a novel structural motif of Brønsted acid catalysts for direct Mannich reaction of N-acyl imines with 1,3-dicarbonyl compounds
    • Terada, M., Sorimachi, K. and Uraguchi, D. (2006) Phosphorodiamidic acid as a novel structural motif of Brønsted acid catalysts for direct Mannich reaction of N-acyl imines with 1,3-dicarbonyl compounds. Synlett, no. 1, 133-136.
    • (2006) Synlett , vol.0 , Issue.1 , pp. 133-136
    • Terada, M.1    Sorimachi, K.2    Uraguchi, D.3
  • 29
    • 33845454140 scopus 로고    scopus 로고
    • On the mechanism of stereoselection in direct Mannich reaction catalyzed by BINOL- derived phosphoric acids
    • Gridnev, I. D., Kouchi, M., Sorimachi, K. and Terada, M. (2007) On the mechanism of stereoselection in direct Mannich reaction catalyzed by BINOL- derived phosphoric acids. Tetrahedron Lett. 48, 497-500.
    • (2007) Tetrahedron Lett , vol.48 , pp. 497-500
    • Gridnev, I.D.1    Kouchi, M.2    Sorimachi, K.3    Terada, M.4
  • 30
    • 23044486704 scopus 로고    scopus 로고
    • Design of an organocatalyst for the enantioselective Diels-Alder reaction with α-acyloxyacroleins
    • (additions and corrections) 13079
    • Ishihara, K. and Nakano, K. (2005) Design of an organocatalyst for the enantioselective Diels-Alder reaction with α-acyloxyacroleins. J. Am. Chem. Soc. 127, 10504-10505, 13079 (additions and corrections).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10504-10505
    • Ishihara, K.1    Nakano, K.2
  • 31
    • 84985635661 scopus 로고
    • First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions
    • Corey, E. J. and Loh, T.-P. (1991) First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions. J. Am. Chem. Soc. 113, 8966-8967.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 8966-8967
    • Corey, E.J.1    Loh, T.-P.2
  • 32
    • 0010510433 scopus 로고
    • Enantioselective Diels-Alder reaction of α-bromo- α,β-enals with dienes under catalysis by CAB
    • Ishihara, K., Gao, Q. and Yamamoto, H. (1993) Enantioselective Diels-Alder reaction of α-bromo- α,β-enals with dienes under catalysis by CAB. J. Org. Chem. 58, 6917-6919.
    • (1993) J. Org. Chem. , vol.58 , pp. 6917-6919
    • Ishihara, K.1    Gao, Q.2    Yamamoto, H.3
  • 33
    • 37049164012 scopus 로고
    • Cyclic disulfides derived from diphenyl
    • Barber, H. J. and Smiles, S. (1928) Cyclic disulfides derived from diphenyl. J. Chem. Soc. 1141-1149.
    • (1928) J. Chem. Soc. , pp. 1141-1149
    • Barber, H.J.1    Smiles, S.2
  • 34
    • 11844279327 scopus 로고
    • Biaryl-2 2'-disulfonic acids and related compounds. III. Optical activity and optical stability in the 1,1'-binaphthyl series
    • Armarego, W. L. F. and Turner, E. E. (1957) Biaryl- 2,2'-disulfonic acids and related compounds. III. Optical activity and optical stability in the 1,1'-binaphthyl series. J. Chem. Soc. 13-22.
    • (1957) J. Chem. Soc. , pp. 13-22
    • Armarego, W.L.F.1    Turner, E.E.2
  • 35
    • 77349112067 scopus 로고    scopus 로고
    • Preparation of optically active binaphthalenesulfonic acids as chiral auxiliary agents
    • Takahashi, K. and Fukushi, K. (2005) Preparation of optically active binaphthalenesulfonic acids as chiral auxiliary agents. Jpn. Patent 2005132815.
    • (2005) Jpn. Patent , pp. 2005132815
    • Takahashi, K.1    Fukushi, K.2
  • 36
    • 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. and Ishihara, K. (2008) 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. 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
  • 37
    • 33751385897 scopus 로고
    • Preparation of enantiomerically pure 1,1'-binaphthalene-2,2'-diol and 1,1'-binaphthalene-2 2'-dithiol
    • Fabbri, D., Delogu, G. and De Lucchi, O. (1993) Preparation of enantiomerically pure 1,1'-binaphthalene-2,2'-diol and 1,1'-binaphthalene-2,2'-dithiol. J. Org. Chem. 58, 1748-1750.
    • (1993) J. Org. Chem. , vol.58 , pp. 1748-1750
    • Fabbri, D.1    Delogu, G.2    De Lucchi, O.3
  • 38
    • 0028205062 scopus 로고
    • Conformational polymorphism and thermorearrangement of 2,2'-bis-O(N,N-dimethylthiocarbamato)-1,1'-binaphthalene. A facile synthesis of 1,1'-binaphthalene-2 2'-dithiol
    • Bandarage, U. K., Simpson, J., Smith, R. A. J. and Weavers, R. T. (1994) Conformational polymorphism and thermorearrangement of 2,2'-bis-O(N,N-dimethylthiocarbamato)-1,1'-binaphthalene. A facile synthesis of 1,1'-binaphthalene-2,2'-dithiol. Tetrahedron 50, 3463-3472.
    • (1994) Tetrahedron , vol.50 , pp. 3463-3472
    • Bandarage, U.K.1    Simpson, J.2    Smith, R.A.J.3    Weavers, R.T.4
  • 40
    • 42149095108 scopus 로고    scopus 로고
    • The Newman-Kwart rearrangement: A microwave kinetic study
    • Gilday, J. P., Lenden, P., Moseley, J. D. and Cox, B. G. (2008) The Newman-Kwart rearrangement: A microwave kinetic study. J. Org. Chem. 73, 3130-3134.
    • (2008) J. Org. Chem , vol.73 , pp. 3130-3134
    • Gilday, J.P.1    Lenden, P.2    Moseley, J.D.3    Cox, B.G.4
  • 41
    • 0010429552 scopus 로고
    • The basecatalysed oxidation of aliphatic and aromatic thiols and disulphides to sulphonic acids
    • Wallace, T. J. and Schriesheim, A. (1965) The basecatalysed oxidation of aliphatic and aromatic thiols and disulphides to sulphonic acids. Tetrahedron 21, 2271-2280.
    • (1965) Tetrahedron , vol.21 , pp. 2271-2280
    • Wallace, T.J.1    Schriesheim, A.2
  • 42
    • 84963163672 scopus 로고
    • A Convenient access to chiral sulfonic acids
    • Agami, C., Prince, B. and Puchot, C. (1990) A Convenient access to chiral sulfonic acids. Synth. Commun. 20, 3289-3294.
    • (1990) Synth. Commun , vol.20 , pp. 3289-3294
    • Agami, C.1    Prince, B.2    Puchot, C.3
  • 43
    • 0001177854 scopus 로고
    • Reaction of β-diketones with peracids
    • House, H. O. and Gannon, W. F. (1958) Reaction of β-diketones with peracids. J. Org. Chem. 23, 879-884.
    • (1958) J. Org. Chem. , vol.23 , pp. 879-884
    • House, H.O.1    Gannon, W.F.2
  • 45
    • 0034600250 scopus 로고    scopus 로고
    • New strategies for organic catalysis: The first highly enantioselective organocatalytic Diels-Alder reaction
    • Arendt, K., Borths, C. J. and MacMillan, D. W. C. (2000) New strategies for organic catalysis: The first highly enantioselective organocatalytic Diels-Alder reaction. J. Am. Chem. Soc. 122, 4243-4244.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4243-4244
    • Arendt, K.1    Borths, C.J.2    MacMillan, D.W.C.3
  • 46
    • 0037139610 scopus 로고    scopus 로고
    • The first general enantioselective catalytic Diels-Alder reaction with simple α,β-unsaturated ketones
    • Northrup, A. B. and MacMillan, D. W. C. (2002) The first general enantioselective catalytic Diels-Alder reaction with simple α,β-unsaturated ketones. J. Am. Chem. Soc. 124, 2458-2460.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2458-2460
    • Northrup, A.B.1    MacMillan, D.W.C.2
  • 47
    • 0000778261 scopus 로고
    • Brønsted acid assisted chiral Lewis acid (BLA) catalyst for asymmetric Diels-Alder reaction
    • Ishihara, K. and Yamamoto, H. (1994) Brønsted acid assisted chiral Lewis acid (BLA) catalyst for asymmetric Diels-Alder reaction. J. Am. Chem. Soc. 116, 1561-1562.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 1561-1562
    • Ishihara, K.1    Yamamoto, H.2
  • 48
    • 0000358324 scopus 로고    scopus 로고
    • A new powerful and practical BLA catalyst for highly enantioselective Diels-Alder reaction: An extreme acceleration of reaction rate by Brønsted acid
    • Ishihara, K., Kurihara, H. and Yamamoto, H. (1996) A new powerful and practical BLA catalyst for highly enantioselective Diels-Alder reaction: An extreme acceleration of reaction rate by Brønsted acid. J. Am. Chem. Soc. 118, 3049-3050.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 3049-3050
    • Ishihara, K.1    Kurihara, H.2    Yamamoto, H.3
  • 49
    • 0032558078 scopus 로고    scopus 로고
    • Design of Brønsted acid- assisted chiral Lewis acid (BLA) catalysts for highly enantioselective Diels-Alder reactions
    • Ishihara, K., Kurihara, H., Matsumoto, M. and Yamamoto, H. (1998) Design of Brønsted acidassisted chiral Lewis acid (BLA) catalysts for highly enantioselective Diels-Alder reactions. J. Am. Chem. Soc. 120, 6920-6930.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 6920-6930
    • Ishihara, K.1    Kurihara, H.2    Matsumoto, M.3    Yamamoto, H.4
  • 50
    • 33745725832 scopus 로고    scopus 로고
    • chiral 1,1'-binaphthyl-2 2'-diammonium salt catalysts for the enantioselective Diels-Alder reaction with α-acyloxyacroleins
    • Sakakura, A., Suzuki, K., Nakano, K. and Ishihara, K. (2006) chiral 1,1'-binaphthyl-2,2'-diammonium salt catalysts for the enantioselective Diels-Alder reaction with α-acyloxyacroleins. Org. Lett. 8, 2229-2232.
    • (2006) Org. Lett. , vol.8 , pp. 2229-2232
    • Sakakura, A.1    Suzuki, K.2    Nakano, K.3    Ishihara, K.4
  • 51
    • 33845274327 scopus 로고    scopus 로고
    • Enantioselective Diels-Alder reaction of α-acyloxyacroleins catalyzed by chiral 1,1'-binaphthyl-2 2'diammonium salts
    • Sakakura, A., Suzuki, K. and Ishihara, K. (2006) Enantioselective Diels-Alder reaction of α-acyloxyacroleins catalyzed by chiral 1,1'-binaphthyl-2,2'diammonium salts. Adv. Synth. Catal. 348, 2457-2465.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 2457-2465
    • Sakakura, A.1    Suzuki, K.2    Ishihara, K.3
  • 52
    • 34547489631 scopus 로고    scopus 로고
    • Enantioselective [2+2] Cycloaddition of unactivated alkenes with α-acyloxyacroleins catalyzed by chiral organoammonium salts
    • Ishihara, K. and Nakano, K. (2007) Enantioselective [2+2] Cycloaddition of unactivated alkenes with α-acyloxyacroleins catalyzed by chiral organoammonium salts. J. Am. Chem. Soc. 129, 8930-8931.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 8930-8931
    • Ishihara, K.1    Nakano, K.2
  • 53
    • 0001368958 scopus 로고
    • Asymmetric [2+2] cycloaddition reaction catalyzed by a chiral titanium reagent
    • Narasaka, K., Hayashi, Y., Shimadzu, H. and Niihata, S. (1992) Asymmetric [2+2] cycloaddition reaction catalyzed by a chiral titanium reagent. J. Am. Chem. Soc. 114, 8869-8885.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 8869-8885
    • Narasaka, K.1    Hayashi, Y.2    Shimadzu, H.3    Niihata, S.4
  • 55
    • 33644902714 scopus 로고    scopus 로고
    • Catalytic enantioselective [2+2]-cycloaddition reaction of 2-methoxycarbonyl-2-cyclopenten- 1-one by chiral copper catalyst
    • Takenaka, Y., Ito, H., Hasegawa, M. and Iguchi, K. (2006) Catalytic enantioselective [2+2]-cycloaddition reaction of 2-methoxycarbonyl-2-cyclopenten1-one by chiral copper catalyst. Tetrahedron 62, 3380-3388.
    • (2006) Tetrahedron , vol.62 , pp. 3380-3388
    • Takenaka, Y.1    Ito, H.2    Hasegawa, M.3    Iguchi, K.4
  • 56
    • 33751551159 scopus 로고    scopus 로고
    • Enantioselective formal synthesis of (+)-precapnelladiene by chiral copper-catalyzed asymmetric [2+2]-cycloaddition reaction
    • Takenaka, Y., Ito, H. and Iguchi, K. (2007) Enantioselective formal synthesis of (+)-precapnelladiene by chiral copper-catalyzed asymmetric [2+2]-cycloaddition reaction. Tetrahedron 63, 510-513.
    • (2007) Tetrahedron , vol.63 , pp. 510-513
    • Takenaka, Y.1    Ito, H.2    Iguchi, K.3
  • 57
    • 33645940266 scopus 로고    scopus 로고
    • Rhcatalyzed enantioselective [2+2] cycloaddition of alkynyl esters and norbornene derivatives
    • Shibata, T., Takami, K. and Kawachi, A. (2006) Rhcatalyzed enantioselective [2+2] cycloaddition of alkynyl esters and norbornene derivatives. Org. Lett. 8, 1343-1345.
    • (2006) Org. Lett. , vol.8 , pp. 1343-1345
    • Shibata, T.1    Takami, K.2    Kawachi, A.3
  • 58
    • 1542377702 scopus 로고    scopus 로고
    • Lewis acid induced tandem Diels-Alder reaction/ring expansion as an equivalent of a [4+3] cycloaddition
    • Davies, H. M. L. and Dai, X. (2004) Lewis acid induced tandem Diels-Alder reaction/ring expansion as an equivalent of a [4+3] cycloaddition. J. Am. Chem. Soc. 126, 2692-2693.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 2692-2693
    • Davies, H.M.L.1    Dai, X.2
  • 59
    • 33845271922 scopus 로고    scopus 로고
    • Formal enantioselective [4+3] cycloaddition by a tandem Diels- Alder reaction/ring expansion
    • Dai, X. and Davies, H. M. L. (2006) Formal enantioselective [4+3] cycloaddition by a tandem Diels- Alder reaction/ring expansion. Adv. Synth. Catal. 348, 2449-2456.
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 2449-2456
    • Dai, X.1    Davies, H.M.L.2
  • 60
    • 25444492377 scopus 로고    scopus 로고
    • Total synthesis of (±)-taiwaniaquinol B via a domino intramolecular friedel|crafts acylation/carbonyl α-tert-alkylation reaction
    • Fillion, E. and Fishlock, D. (2005) Total synthesis of (±)-taiwaniaquinol B via a domino intramolecular friedel|crafts acylation/carbonyl α-tert-alkylation reaction. J. Am. Chem. Soc. 127, 13144-13145.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 13144-13145
    • Fillion, E.1    Fishlock, D.2
  • 61
    • 33645499302 scopus 로고    scopus 로고
    • General route to 4a-methylhydrofluorene diterpenoids: Total syntheses of (±)- taiwaniaquinones D and H, (±)-taiwaniaquinol B, (±)-dichroanal B, and (±)-dichroanone
    • Banerjee, M., Mukhopadhyay, R., Achari, B. and Banerjee, A. K. (2006) General route to 4a-methylhydrofluorene diterpenoids: Total syntheses of (±)- taiwaniaquinones D and H, (±)-taiwaniaquinol B, (±)-dichroanal B, and (±)-dichroanone. J. Org. Chem. 71, 2787-2796.
    • (2006) J. Org. Chem. , vol.71 , pp. 2787-2796
    • Banerjee, M.1    Mukhopadhyay, R.2    Achari, B.3    Banerjee, A.K.4
  • 62
    • 33748089380 scopus 로고    scopus 로고
    • Synthesis of taiwaniaquinoids via Nazarov trifiation
    • Liang, G., Xu, Y., Seiple, I. B. and Trauner, D. (2006) Synthesis of taiwaniaquinoids via Nazarov trifiation. J. Am. Chem. Soc. 128, 11022-11023.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 11022-11023
    • Liang, G.1    Xu, Y.2    Seiple, I.B.3    Trauner, D.4
  • 63
    • 33745417849 scopus 로고    scopus 로고
    • The catalytic enantioselective, protecting group-free total synthesis of (+)-dichroanone
    • McFadden, R. M. and Stoltz, B. M. (2006) The catalytic enantioselective, protecting group-free total synthesis of (+)-dichroanone. J. Am. Chem. Soc. 128, 7738-7739.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 7738-7739
    • McFadden, R.M.1    Stoltz, B.M.2
  • 64
    • 0026343779 scopus 로고
    • Asymmetric synthesis of 2-aminonorbornane-2- carboxylic acids by Diels-Alder reaction
    • Cativiela, C., López, P. and Mayoral, J. A. (1991) Asymmetric synthesis of 2-aminonorbornane-2- carboxylic acids by Diels-Alder reaction. Tetrahedron: Asymmetry 2, 1295-1304.
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 1295-1304
    • Cativiela, C.1    López, P.2    Mayoral, J.A.3
  • 65
    • 51649091188 scopus 로고    scopus 로고
    • Organocatalytic enantioselective Diels-Alder reaction of dienes with α-(N N-diacylamino)acroleins
    • Ishihara, K., Nakano, K. and Akakura, M. (2008) Organocatalytic enantioselective Diels-Alder reaction of dienes with α-(N,N-diacylamino)acroleins. Org. Lett. 10, 2893-2896.
    • (2008) Org. Lett. , vol.10 , pp. 2893-2896
    • Ishihara, K.1    Nakano, K.2    Akakura, M.3
  • 66
    • 0033529741 scopus 로고    scopus 로고
    • A highly diastereoselective approach to conformationally constrained serine analogues: Synthesis of an α-amino-β-hydroxycyclohexenecarboxylic acid and derivatives
    • Clerici, F., Gelmi, M. L. and Gambini, A. (1999) A highly diastereoselective approach to conformationally constrained serine analogues: Synthesis of an a-amino-β-hydroxycyclohexenecarboxylic acid and derivatives. J. Org. Chem. 64, 5764-5767.
    • (1999) J. Org. Chem. , vol.64 , pp. 5764-5767
    • Clerici, F.1    Gelmi, M.L.2    Gambini, A.3
  • 67
    • 0034618229 scopus 로고    scopus 로고
    • Diels-Alder approach to tetraline-based constrained α-amino acid derivatives
    • Kotha, S., Ganesh, T. and Ghosh, A. K. (2000) Diels-Alder approach to tetraline-based constrained α-amino acid derivatives. Bioorg. Med. Chem. Lett. 10, 1755-1757.
    • (2000) Bioorg. Med. Chem. Lett , vol.10 , pp. 1755-1757
    • Kotha, S.1    Ganesh, T.2    Ghosh, A.K.3
  • 68
    • 0035939186 scopus 로고    scopus 로고
    • Carbocyclic serine analogues: Regioand diastereoselective syntheses of new 1-amino-2 5-dihydroxycyclohexanecarboxylic acids
    • Clerici, F., Gelmi, M. L., Gambini, A. and Nava, D. (2001) Carbocyclic serine analogues: Regio- and diastereoselective syntheses of new 1-amino-2,5-dihydroxycyclohexanecarboxylic acids. Tetrahedron 57, 6429-6438.
    • (2001) Tetrahedron , vol.57 , pp. 6429-6438
    • Clerici, F.1    Gelmi, M.L.2    Gambini, A.3    Nava, D.4
  • 69
    • 15944420883 scopus 로고    scopus 로고
    • Highly regioselective Diels-Alder reactions of 9-substituted anthracenes and 2-acetamidoacrylate: Synthesis of conformationally constrained α-amino acids
    • Yang, B. V. and Doweyko, L. M. (2005) Highly regioselective Diels-Alder reactions of 9-substituted anthracenes and 2-acetamidoacrylate: Synthesis of conformationally constrained α-amino acids. Tetrahedron Lett. 46, 2857-2860.
    • (2005) Tetrahedron Lett , vol.46 , pp. 2857-2860
    • Yang, B.V.1    Doweyko, L.M.2
  • 70
    • 0034712270 scopus 로고    scopus 로고
    • Stereoselective synthesis of quaternary α-amino acids Part 2 Cyclic compounds
    • Cativiela, C. and Díaz-de-Villegas, M. D. (2000) Stereoselective synthesis of quaternary α-amino acids. Part 2: Cyclic compounds. Tetrahedron: Asymmetry 11, 645-732.
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 645-732
    • Cativiela, C.1    Díaz-de-Villegas, M.D.2
  • 71
    • 0030447297 scopus 로고    scopus 로고
    • An efficient synthesis of 6-substituted aminohexahydro-1H-1 4-diazepines from 2-substituted aminopropenals
    • Harada, H., Morie, T., Hirokawa, Y. and Kato, S. (1996) An efficient synthesis of 6-substituted aminohexahydro-1H-1, 4-diazepines from 2-substituted aminopropenals. Chem. Pharm. Bull. 44, 2205- 2212.
    • (1996) Chem. Pharm. Bull. , vol.44 , pp. 2205-2212
    • Harada, H.1    Morie, T.2    Hirokawa, Y.3    Kato, S.4
  • 72
    • 0026024383 scopus 로고
    • A synthesis of 2-endo-amino-2-exo-hydroxymethylnorbornenes having inhibitory activity against protein kinase C
    • Iwasaki, T., Yamazaki, H., Nishitani, T. and Sato, T. (1991) A synthesis of 2-endo-amino-2-exo-hydroxymethylnorbornenes having inhibitory activity against protein kinase C. Chem. Pharm. Bull. 39, 527-529.
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 527-529
    • Iwasaki, T.1    Yamazaki, H.2    Nishitani, T.3    Sato, T.4
  • 74
    • 0028785752 scopus 로고
    • Total synthesis of (-)-altemicidin: A novel exploitation of the Potier-Polonovski rearrangement
    • Kende, A. S., Liu, K. and Jos Brands, K. M. (1995) Total synthesis of (-)-altemicidin: A novel exploitation of the Potier-Polonovski rearrangement. J. Am. Chem. Soc. 117, 10597-10598.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10597-10598
    • Kende, A.S.1    Liu, K.2    Jos Brands, K.M.3


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