메뉴 건너뛰기




Volumn 15, Issue 24, 2011, Pages 4083-4107

Nucleophilic tertiary phosphine organocatalysts in asymmetric reactions

Author keywords

Desymmetrization; Diastereoselective reaction; Enantioselective reaction; Kinetic resolution; Organocatalysis; Phosphine

Indexed keywords

ENANTIOSELECTIVITY; PHOSPHORUS COMPOUNDS; REACTION KINETICS; STEREOSELECTIVITY;

EID: 81255211555     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211798109222     Document Type: Review
Times cited : (24)

References (112)
  • 2
    • 5144220014 scopus 로고    scopus 로고
    • Nucleophilic phosphine organocatalysis
    • Methot, J. T.; Roush, W. R. Nucleophilic phosphine organocatalysis. Adv. Synth. Catal., 2004, 346, 1035-1050.
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1035-1050
    • Methot, J.T.1    Roush, W.R.2
  • 3
    • 33748276229 scopus 로고
    • Ueber Ähnlichkeiten in der katalytischen Wirkung von Fermenten und von definierten organischen Stoffen
    • Langenbeck, W. Ueber Ähnlichkeiten in der katalytischen Wirkung von Fermenten und von definierten organischen Stoffen. Angew. Chem., 1928, 41, 740-745.
    • (1928) Angew. Chem. , vol.41 , pp. 740-745
    • Langenbeck, W.1
  • 5
    • 84981789229 scopus 로고
    • Asymmetric catalytic hydrogenation with an optically active phosphinerhodium complex in homogeneous solution
    • Hornor, L.; Siegel, H.; Büthe, H. Asymmetric catalytic hydrogenation with an optically active phosphinerhodium complex in homogeneous solution. Angew. Chem Int. Ed., 1968, 7, 942-942.
    • (1968) Angew. Chem Int. Ed. , vol.7 , pp. 942-942
    • Hornor, L.1    Siegel, H.2    Büthe, H.3
  • 6
    • 33444462389 scopus 로고
    • Catalytic asymmetric hydrogenation employing a soluble, optically active, rhodium complex
    • Knowles, W. S.; Sabacky, M. J. Catalytic asymmetric hydrogenation employing a soluble, optically active, rhodium complex. J. Chem. Soc., Chem. Commun., 1968, 1445-1446.
    • (1968) J. Chem. Soc., Chem. Commun. , pp. 1445-1446
    • Knowles, W.S.1    Sabacky, M.J.2
  • 8
    • 34347262098 scopus 로고    scopus 로고
    • The enantioselective Morita-Baylis- Hillman reaction and its aza counterpart
    • Masson, G.; Housseman, C.; Zhu, J. The enantioselective Morita-Baylis- Hillman reaction and its aza counterpart. Angew. Chem. Int. Ed., 2007, 46, 4614-4628.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 4614-4628
    • Masson, G.1    Housseman, C.2    Zhu, J.3
  • 9
    • 34347355605 scopus 로고    scopus 로고
    • Aza-Baylis-Hillman reactions and their synthetic applications
    • Shi, Y.-L.; Shi, M. Aza-Baylis-Hillman reactions and their synthetic applications. Eur. J. Org. Chem., 2007, 2905-2916.
    • (2007) Eur. J. Org. Chem. , pp. 2905-2916
    • Shi, Y.-L.1    Shi, M.2
  • 10
    • 0037150594 scopus 로고    scopus 로고
    • Diastereoselective Baylis-Hillman type reactions of chiral non-racemic N-sulfinimines with cyclopent-2-en-1-one
    • Shi, M.; Xu, Y.-M. Diastereoselective Baylis-Hillman type reactions of chiral non-racemic N-sulfinimines with cyclopent-2-en-1-one. Tetrahedron: Asymmetry, 2002, 13, 1195-1200.
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 1195-1200
    • Shi, M.1    Xu, Y.-M.2
  • 11
    • 50649124427 scopus 로고    scopus 로고
    • Chiral N-thiophosphoryl imine-induced diastereoselective aza-Morita-Baylis-Hillman reaction
    • Lu, A. D.; Xu, X. Y.; Gao, P.; Zhou, Z. H.; Song, H. B.; Tang, C. C. Chiral N-thiophosphoryl imine-induced diastereoselective aza-Morita-Baylis-Hillman reaction. Tetrahedron: Asymmetry, 2008, 19, 1886-1890.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 1886-1890
    • Lu, A.D.1    Xu, X.Y.2    Gao, P.3    Zhou, Z.H.4    Song, H.B.5    Tang, C.C.6
  • 12
    • 5144227748 scopus 로고
    • U.S. Patent 3,074,999, 1963
    • Rauhut, M.; Currier, H. U.S. Patent 3,074,999, 1963; Chem. Abstr. 1963, 58, 11224a.
    • (1963) Chem. Abstr. , vol.58 , pp. 11224
    • Rauhut, M.1    Currier, H.2
  • 13
    • 0037026517 scopus 로고    scopus 로고
    • Application of the intramolecular vinylogous Morita-Baylis-Hillman reaction toward the synthesis of the spinosyn A tricyclic nucleus
    • Mergott, D. J.; Frank, S. A.; Roush, W. R. Application of the intramolecular vinylogous Morita-Baylis-Hillman reaction toward the synthesis of the spinosyn A tricyclic nucleus. Org. Lett., 2002, 4, 3157-3160.
    • (2002) Org. Lett. , vol.4 , pp. 3157-3160
    • Mergott, D.J.1    Frank, S.A.2    Roush, W.R.3
  • 14
    • 0344944868 scopus 로고    scopus 로고
    • Synthetic studies toward FR182877. Remarkable solvent efect in the vinylogous Morita-Baylis-Hillman cyclization
    • Methot, J. L.; Roush, W. R. Synthetic studies toward FR182877. Remarkable solvent efect in the vinylogous Morita-Baylis-Hillman cyclization. Org. Lett., 2003, 5, 4223-4226.
    • (2003) Org. Lett. , vol.5 , pp. 4223-4226
    • Methot, J.L.1    Roush, W.R.2
  • 15
    • 41149157530 scopus 로고    scopus 로고
    • Total synthesis of (-)-Spinosyn A: Examination of structural features that govern the stereoselectivity of the key transannular Diels-Alder reaction
    • Winbush, S. M.; Mergott, D. J.; Roush, W. R. Total synthesis of (-)-Spinosyn A: Examination of structural features that govern the stereoselectivity of the key transannular Diels-Alder reaction. J. Org. Chem., 2008, 73, 1818-1829.
    • (2008) J. Org. Chem. , vol.73 , pp. 1818-1829
    • Winbush, S.M.1    Mergott, D.J.2    Roush, W.R.3
  • 16
    • 0034283585 scopus 로고    scopus 로고
    • New strategies for the development of an asymmetric version of the Baylis-Hillman reaction
    • Langer, P. New strategies for the development of an asymmetric version of the Baylis-Hillman reaction. Angew. Chem. Int. Ed., 2000, 39, 3049-3052.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3049-3052
    • Langer, P.1
  • 17
    • 15744371754 scopus 로고    scopus 로고
    • Recent advances progresses in the asymmetric Baylis-Hillman reaction
    • (in chinese)
    • Cai, J. X.; Zhou, Z. H.; Tang, C. C. Recent advances progresses in the asymmetric Baylis-Hillman reaction. Chem. Res., 2001, 12, 54-64 (in chinese).
    • (2001) Chem. Res. , vol.12 , pp. 54-64
    • Cai, J.X.1    Zhou, Z.H.2    Tang, C.C.3
  • 18
    • 0037366617 scopus 로고    scopus 로고
    • Recent advances in the Baylis-Hillman reaction and applications
    • Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Recent advances in the Baylis-Hillman reaction and applications. Chem. Rev., 2003, 103, 811-892.
    • (2003) Chem. Rev. , vol.103 , pp. 811-892
    • Basavaiah, D.1    Rao, A.J.2    Satyanarayana, T.3
  • 19
    • 34548185871 scopus 로고    scopus 로고
    • The Baylis-Hillman reaction: A novel source of attraction, opportunities, and challenges in synthetic chemistry
    • Basavaiah, D.; Rao, V. K.; Reddy, R. J. The Baylis-Hillman reaction: A novel source of attraction, opportunities, and challenges in synthetic chemistry. Chem. Soc. Rew., 2007, 36, 1581-1588.
    • (2007) Chem. Soc. Rew. , vol.36 , pp. 1581-1588
    • Basavaiah, D.1    Rao, V.K.2    Reddy, R.J.3
  • 20
    • 0001461985 scopus 로고
    • A tertiary phosphine-catalyzed reaction of acrylic compounds with aldehydes
    • Morita, K.; Suzuki, Z.; Hirose, H. A tertiary phosphine-catalyzed reaction of acrylic compounds with aldehydes. Bull. Chem. Soc. Jpn., 1968, 41, 2815-2815.
    • (1968) Bull. Chem. Soc. Jpn. , vol.41 , pp. 2815-2815
    • Morita, K.1    Suzuki, Z.2    Hirose, H.3
  • 22
    • 0026505236 scopus 로고
    • An intramolecular Baylis-Hillman reaction
    • Roth, F.; Gygax, P.; Fráter, G. An intramolecular Baylis-Hillman reaction. Tetrahedron Lett., 1992, 33, 1045-1048.
    • (1992) Tetrahedron Lett , vol.33 , pp. 1045-1048
    • Roth, F.1    Gygax, P.2    Fráter, G.3
  • 23
    • 0001161458 scopus 로고    scopus 로고
    • An enantioselective Baylis-Hillman reaction catalyzed by chiral phosphines under atmospheric pressure
    • Hayase, T.; Shibata, T.; Soai, K.; Wakatsuki, Y. An enantioselective Baylis-Hillman reaction catalyzed by chiral phosphines under atmospheric pressure. Chem. Commun., 1998, 1271-1272.
    • (1998) Chem. Commun. , pp. 1271-1272
    • Hayase, T.1    Shibata, T.2    Soai, K.3    Wakatsuki, Y.4
  • 24
    • 0034595938 scopus 로고    scopus 로고
    • Synthesis of chiral hydroxyl phospholanes from D-mannitol and their use in asymmetric catalytic reactions
    • Li, W. G.; Zhang, Z. G.; Xiao, D. M.; Zhang, X. M. Synthesis of chiral hydroxyl phospholanes from D-mannitol and their use in asymmetric catalytic reactions. J. Org. Chem., 2000, 65, 3489-3496.
    • (2000) J. Org. Chem. , vol.65 , pp. 3489-3496
    • Li, W.G.1    Zhang, Z.G.2    Xiao, D.M.3    Zhang, X.M.4
  • 25
    • 0034719742 scopus 로고    scopus 로고
    • Efficient Baylis-Hillman reactions promoted by mild cooperative catalysts and their application to catalytic asymmetric synthesis
    • Yamada, Y. M. A.; Ikegami, S. Efficient Baylis-Hillman reactions promoted by mild cooperative catalysts and their application to catalytic asymmetric synthesis. Tetrahedron Lett., 2000, 41, 2165-2169.
    • (2000) Tetrahedron Lett , vol.41 , pp. 2165-2169
    • Yamada, Y.M.A.1    Ikegami, S.2
  • 26
    • 28044437774 scopus 로고    scopus 로고
    • Ferrocenylphosphines as new catalysts for Baylis-Hillman reactions
    • Pereira, S. I.; Adrio, J.; Silva, A. M. S.; Carretero, J. C. Ferrocenylphosphines as new catalysts for Baylis-Hillman reactions. J. Org. Chem., 2005, 70, 10175-10177.
    • (2005) J. Org. Chem. , vol.70 , pp. 10175-10177
    • Pereira, S.I.1    Adrio, J.2    Silva, A.M.S.3    Carretero, J.C.4
  • 27
    • 0141923582 scopus 로고    scopus 로고
    • Asymmetric Morita-Baylis-Hillman Reactions Catalyzed by Chiral Brønsted Acids
    • McDougal, N. T.; Schaus, S. E. Asymmetric Morita-Baylis-Hillman Reactions Catalyzed by Chiral Brønsted Acids. J. Am. Chem. Soc., 2003, 125, 12094-12095.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 12094-12095
    • McDougal, N.T.1    Schaus, S.E.2
  • 28
    • 5144219609 scopus 로고    scopus 로고
    • The development of the asymmetric Morita-Baylis-Hillman reaction catalyzed by chiral Brønsted acids
    • McDougal, N. T.; Trevellini, W. L.; Rodgen, S. A.; Kliman, L. T.; Schaus, S. E. The development of the asymmetric Morita-Baylis-Hillman reaction catalyzed by chiral Brønsted acids. Adv. Synth. Catal., 2004, 346, 1231-1240.
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1231-1240
    • McDougal, N.T.1    Trevellini, W.L.2    Rodgen, S.A.3    Kliman, L.T.4    Schaus, S.E.5
  • 29
    • 33846286469 scopus 로고    scopus 로고
    • Asymmetric catalysis of Morita-Baylis-Hillman reactions by chiral phosphine Lewis bases bearing multiple phenol groups
    • Shi, M.; Liu, Y.-H.; Chen, L.-H. Asymmetric catalysis of Morita-Baylis-Hillman reactions by chiral phosphine Lewis bases bearing multiple phenol groups. Chirality, 2007, 19, 124-128.
    • (2007) Chirality , vol.19 , pp. 124-128
    • Shi, M.1    Liu, Y.-H.2    Chen, L.-H.3
  • 30
    • 51449114658 scopus 로고    scopus 로고
    • Bifunctional chiral phosphinecontaining Lewis base catalyzed asymmetric Morita-Baylis-Hillman reaction of aldehydes with activated alkenes
    • Lei, Z.-Y.; Liu, X.-G.; Shi, M.; Zhao, M.-X. Bifunctional chiral phosphinecontaining Lewis base catalyzed asymmetric Morita-Baylis-Hillman reaction of aldehydes with activated alkenes. Tetrahedron: Asymmetry, 2008, 19, 2058-2062.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 2058-2062
    • Lei, Z.-Y.1    Liu, X.-G.2    Shi, M.3    Zhao, M.-X.4
  • 31
    • 50949101490 scopus 로고    scopus 로고
    • Chiral phosphinothiourea organocatalyst in the enantioselective Morita-Baylis-Hillman reactions of aromatic aldehydes with methyl vinyl ketone
    • Yuan, K.; Zhang, L.; Song, H.-L.; Hu, Y. J.; Wu, X.-Y. Chiral phosphinothiourea organocatalyst in the enantioselective Morita-Baylis-Hillman reactions of aromatic aldehydes with methyl vinyl ketone. Tetrahedron Lett., 2008, 49, 6262-6264.
    • (2008) Tetrahedron Lett , vol.49 , pp. 6262-6264
    • Yuan, K.1    Zhang, L.2    Song, H.-L.3    Hu, Y.J.4    Wu, X.-Y.5
  • 32
    • 69049101105 scopus 로고    scopus 로고
    • Chiral phosphinothioureacatalyzed asymmetric Morita-Baylis-Hillman reactions of acrylates with aromatic aldehydes
    • Yuan, K.; Song, H.-L.; Hu, Y.-J.; Wu, X.-Y. Chiral phosphinothioureacatalyzed asymmetric Morita-Baylis-Hillman reactions of acrylates with aromatic aldehydes. Tetrahedron, 2009, 65, 8185-8190.
    • (2009) Tetrahedron , vol.65 , pp. 8185-8190
    • Yuan, K.1    Song, H.-L.2    Hu, Y.-J.3    Wu, X.-Y.4
  • 34
    • 0038696449 scopus 로고    scopus 로고
    • Chiral phosphine Lewis base catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone and phenyl acrylate
    • Shi, M.; Chen, L.-H. Chiral phosphine Lewis base catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone and phenyl acrylate. Chem. Commun., 2003, 1310-1311.
    • (2003) Chem. Commun. , pp. 1310-1311
    • Shi, M.1    Chen, L.-H.2
  • 35
    • 15744383666 scopus 로고    scopus 로고
    • Chiral phosphine Lewis bases catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins
    • Shi, M.; Chen, L.-H.; Li, C.-Q. Chiral phosphine Lewis bases catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins. J. Am. Chem. Soc., 2005, 127, 3790-3800.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 3790-3800
    • Shi, M.1    Chen, L.-H.2    Li, C.-Q.3
  • 36
    • 5144223758 scopus 로고    scopus 로고
    • Aza-Baylis-Hillman reactions of N-(arylmethylene)diphenylphosphinamides with activated olefins in the presence of various Lewis bases
    • Shi, M.; Zhao G.-L. Aza-Baylis-Hillman reactions of N-(arylmethylene)diphenylphosphinamides with activated olefins in the presence of various Lewis bases. Adv. Synth. Catal., 2004, 346, 1205-1219.
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1205-1219
    • Shi, M.1    Zhao, G.-L.2
  • 37
    • 36849076719 scopus 로고    scopus 로고
    • Chiral bifunctional organocatalysts in asymmetric aza-Morita-Baylis-Hillman reactions of ethyl (arylimino)acetates with methyl vinyl ketone and ethyl vinyl ketone
    • Shi, M.; Ma, G.-N.; Gao, J. Chiral bifunctional organocatalysts in asymmetric aza-Morita-Baylis-Hillman reactions of ethyl (arylimino)acetates with methyl vinyl ketone and ethyl vinyl ketone. J. Org. Chem., 2007, 72, 9779-9781.
    • (2007) J. Org. Chem. , vol.72 , pp. 9779-9781
    • Shi, M.1    Ma, G.-N.2    Gao, J.3
  • 38
    • 27544493994 scopus 로고    scopus 로고
    • Catalytic, asymmetric aza-Baylis-Hillman reaction of Nsulfonated imines with 2-cyclohexen-1-one and 2-cyclopenten-1-one in the presence of a chiral phosphine Lewis base
    • Shi, M.; Li, C.-Q. Catalytic, asymmetric aza-Baylis-Hillman reaction of Nsulfonated imines with 2-cyclohexen-1-one and 2-cyclopenten-1-one in the presence of a chiral phosphine Lewis base. Tetrahedron: Asymmetry, 2005, 16, 1385-1391.
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 1385-1391
    • Shi, M.1    Li, C.-Q.2
  • 39
    • 28244436733 scopus 로고    scopus 로고
    • Asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone catalyzed by chiral phosphine Lewis bases bearing perfluoroalkanes as "pony tails"
    • Shi, M.; Chen, L.-H.; Teng, W.-D. Asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone catalyzed by chiral phosphine Lewis bases bearing perfluoroalkanes as "pony tails". Adv. Synth. Catal., 2005, 347, 1781-1789.
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 1781-1789
    • Shi, M.1    Chen, L.-H.2    Teng, W.-D.3
  • 40
    • 51449083032 scopus 로고    scopus 로고
    • A fast catalytic asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone in the presence of chiral bifunctional phosphane Lewis bases
    • Lei, Z.-Y.; Ma, G. N.; Shi, M. A fast catalytic asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone in the presence of chiral bifunctional phosphane Lewis bases. Eur. J. Org. Chem., 2008, 3817-3820.
    • (2008) Eur. J. Org. Chem. , pp. 3817-3820
    • Lei, Z.-Y.1    Ma, G.N.2    Shi, M.3
  • 41
    • 33744818862 scopus 로고    scopus 로고
    • Asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with activated olefins catalyzed by chiral phosphine Lewis bases bearing multiple phenol groups
    • Liu, Y.-H.; Chen, L.-H.; Shi, M. Asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with activated olefins catalyzed by chiral phosphine Lewis bases bearing multiple phenol groups. Adv. Synth. Catal., 2006, 348, 973-979.
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 973-979
    • Liu, Y.-H.1    Chen, L.-H.2    Shi, M.3
  • 42
    • 33645395732 scopus 로고    scopus 로고
    • A Brønsted acid and Lewis base organocatalyst for the aza-Morita-Baylis-Hillman Reaction
    • Matsui, K.; Takizawa, S.; Sasai, H. A Brønsted acid and Lewis base organocatalyst for the aza-Morita-Baylis-Hillman Reaction. Synlett, 2006, 761-765.
    • (2006) Synlett , pp. 761-765
    • Matsui, K.1    Takizawa, S.2    Sasai, H.3
  • 43
    • 34547599687 scopus 로고    scopus 로고
    • Highly enantioselective aza-Morita-Baylis- Hillman reaction with a bisphenol-based bifunctional organocatalyst
    • Ito, K.; Nishida, K.; Gotanda, T. Highly enantioselective aza-Morita-Baylis- Hillman reaction with a bisphenol-based bifunctional organocatalyst. Tetrahedron Lett., 2007, 48, 6147-6149.
    • (2007) Tetrahedron Lett , vol.48 , pp. 6147-6149
    • Ito, K.1    Nishida, K.2    Gotanda, T.3
  • 44
    • 85196432635 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 45
    • 29844448114 scopus 로고    scopus 로고
    • Recognition and activation by ureas and thioureas: Stereoselective reactions using ureas and thioureas as hydrogenbonding donors
    • Takemoto, Y. Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogenbonding donors. Org. Biomol. Chem., 2005, 3, 4299-4306.
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 4299-4306
    • Takemoto, Y.1
  • 46
    • 33746277515 scopus 로고    scopus 로고
    • Organocatalysis mediated by (thio)urea derivatives
    • Connon, S. J. Organocatalysis mediated by (thio)urea derivatives. Chem. Eur. J., 2006, 12, 5418-5427.
    • (2006) Chem. Eur. J , vol.12 , pp. 5418-5427
    • Connon, S.J.1
  • 47
    • 85196435031 scopus 로고    scopus 로고
    • For computational studies, see
    • For computational studies, see
  • 48
    • 84962467066 scopus 로고    scopus 로고
    • Theoretical studies on the bifunctionality of chiral thiourea-based organocatalysts: Competing routes to C-C bond formation
    • A. Hamza, G. Schubert, T. Soós, I. Pápai, Theoretical studies on the bifunctionality of chiral thiourea-based organocatalysts: Competing routes to C-C bond formation. J. Am. Chem. Soc., 2006, 128, 13151-13160.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 13151-13160
    • Hamza, A.1    Schubert, G.2    Soós, T.3    Pápai, I.4
  • 49
    • 25444432564 scopus 로고    scopus 로고
    • Chiral binaphthyl-derived amine-thiourea organocatalyst-promoted asymmetric Morita-Baylis- Hillman reaction
    • Wang, J.; Li, H.; Yu, X.; Zu, L.; Wang, W. Chiral binaphthyl-derived amine-thiourea organocatalyst-promoted asymmetric Morita-Baylis- Hillman reaction. Org. Lett., 2005, 7, 4293-4296.
    • (2005) Org. Lett. , vol.7 , pp. 4293-4296
    • Wang, J.1    Li, H.2    Yu, X.3    Zu, L.4    Wang, W.5
  • 50
    • 3042579804 scopus 로고    scopus 로고
    • Development of bis-thiourea-type organocatalyst for asymmetric Baylis-Hillman reaction
    • Sohtome, Y.; Tanatani, A.; Hashimoto, Y.; Nagasawa, K. Development of bis-thiourea-type organocatalyst for asymmetric Baylis-Hillman reaction. Tetrahedron Lett., 2004, 45, 5589-5592.
    • (2004) Tetrahedron Lett , vol.45 , pp. 5589-5592
    • Sohtome, Y.1    Tanatani, A.2    Hashimoto, Y.3    Nagasawa, K.4
  • 51
    • 33748989516 scopus 로고    scopus 로고
    • Asymmetric Morita-Baylis-Hillman reaction catalyzed by isophoronediamine-derived bis(thio)urea organocatalysts
    • Berkessel, A.; Roland, K.; Neudörfl, J. M. Asymmetric Morita-Baylis-Hillman reaction catalyzed by isophoronediamine-derived bis(thio)urea organocatalysts. Org. Lett., 2006, 8, 4195-4198.
    • (2006) Org. Lett. , vol.8 , pp. 4195-4198
    • Berkessel, A.1    Roland, K.2    Neudörfl, J.M.3
  • 52
    • 27544480807 scopus 로고    scopus 로고
    • Highly enantioselective aza-Baylis-Hillman reactions catalyzed by chiral thiourea derivatives
    • Raheem, I. T.; Jacobsen, E. N. Highly enantioselective aza-Baylis-Hillman reactions catalyzed by chiral thiourea derivatives. Adv. Synth. Catal., 2005, 347, 1701-1708.
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 1701-1708
    • Raheem, I.T.1    Jacobsen, E.N.2
  • 53
    • 34948840851 scopus 로고    scopus 로고
    • Chiral Thiourea-phosphine organocatalysts in the asymmetric aza-Morita-Baylis-Hillman reaction
    • Shi, Y.-L.; Shi, M. Chiral Thiourea-phosphine organocatalysts in the asymmetric aza-Morita-Baylis-Hillman reaction. Adv. Synth. Catal., 2007, 349, 2129-2135.
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 2129-2135
    • Shi, Y.-L.1    Shi, M.2
  • 54
    • 37649015237 scopus 로고    scopus 로고
    • Asymmetric catalytic aza-MoritaeBayliseHillman reaction using chiral bifunctional phosphine amides as catalysts
    • Qi, M.-J.; Ai, T.; Shi, M.; Li, G. G. Asymmetric catalytic aza-MoritaeBayliseHillman reaction using chiral bifunctional phosphine amides as catalysts. Tetrahedron, 2008, 64, 1181-1186.
    • (2008) Tetrahedron , vol.64 , pp. 1181-1186
    • Qi, M.-J.1    Ai, T.2    Shi, M.3    Li, G.G.4
  • 55
    • 50649095554 scopus 로고    scopus 로고
    • Chiral sterically congested phosphaneamide bifunctional organocatalysts in asymmetric aza-Morita-Baylis-Hillman reactions of N-sulfonated imines with methyl and ethyl vinyl ketones
    • Guan, X.-Y.; Jiang, Y. Q.; Shi, M. Chiral sterically congested phosphaneamide bifunctional organocatalysts in asymmetric aza-Morita-Baylis-Hillman reactions of N-sulfonated imines with methyl and ethyl vinyl ketones. Eur. J. Org. Chem., 2008, 2150-2155.
    • (2008) Eur. J. Org. Chem. , pp. 2150-2155
    • Guan, X.-Y.1    Jiang, Y.Q.2    Shi, M.3
  • 56
    • 85196435218 scopus 로고    scopus 로고
    • For most recent reviews for dendritic catalysts, see
    • For most recent reviews for dendritic catalysts, see
  • 57
    • 33846222370 scopus 로고    scopus 로고
    • Peptide dendrimers as artificial enzymes, receptors, and drug-delivery agents
    • Darbre,T.; Reymond, J.-L. Peptide dendrimers as artificial enzymes, receptors, and drug-delivery agents. Acc. Chem. Res., 2006, 39, 925-934.
    • (2006) Acc. Chem. Res. , vol.39 , pp. 925-934
    • Darbre, T.1    Reymond, J.-L.2
  • 58
    • 34248347357 scopus 로고    scopus 로고
    • Development of dendrimers: Macromole-cules for use in organic lightemitting diodes and solar cells
    • Lo, S.-C.; Burn, P. L. Development of dendrimers: Macromole-cules for use in organic lightemitting diodes and solar cells. Chem. Rev., 2007, 107, 1097-1116.
    • (2007) Chem. Rev. , vol.107 , pp. 1097-1116
    • Lo, S.-C.1    Burn, P.L.2
  • 59
    • 38349116542 scopus 로고    scopus 로고
    • Dendritic chiral phosphine Lewis bases-catalyzed asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with activated olefins
    • Liu, Y.-H.; Shi, M. Dendritic chiral phosphine Lewis bases-catalyzed asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with activated olefins. Adv. Synth. Catal., 2008, 350, 122-128.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 122-128
    • Liu, Y.-H.1    Shi, M.2
  • 60
    • 60849113441 scopus 로고    scopus 로고
    • Enantioselective trifunctional organocatalysts for rate-enhanced aza-Morita-Baylis-Hillman reactions at room temperature
    • Garnier, J.-M.; Anstiss, C.; Liu, F. Enantioselective trifunctional organocatalysts for rate-enhanced aza-Morita-Baylis-Hillman reactions at room temperature Adv. Synth. Catal., 2009, 351, 331-338.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 331-338
    • Garnier, J.-M.1    Anstiss, C.2    Liu, F.3
  • 61
    • 67649403306 scopus 로고    scopus 로고
    • Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-Morita-Baylis-Hillman reactions at ambient temperature
    • Garnier, J.-M.; Liu, F. Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-Morita-Baylis-Hillman reactions at ambient temperature. Org. Biomol. Chem., 2009, 7, 1272-1275.
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 1272-1275
    • Garnier, J.-M.1    Liu, F.2
  • 63
    • 33751156723 scopus 로고
    • Phosphine-catalyzed cycloaddition of 2,3-butadienoates or 2-butynoates with electron-deficient olefins. A novel [3+2] annulation approach to cyclopentenes
    • Zhang, C.; Lu, X. Phosphine-catalyzed cycloaddition of 2,3-butadienoates or 2-butynoates with electron-deficient olefins. A novel [3+2] annulation approach to cyclopentenes. J. Org. Chem., 1995, 60, 2906-2908.
    • (1995) J. Org. Chem. , vol.60 , pp. 2906-2908
    • Zhang, C.1    Lu, X.2
  • 64
    • 0037073879 scopus 로고    scopus 로고
    • Highly regioselective construction of spirocycles via phosphine-catalyzed [3+2]-cycloaddition
    • Du, Y.; Lu, X.; Yu, Y. Highly regioselective construction of spirocycles via phosphine-catalyzed [3+2]-cycloaddition. J. Org. Chem., 2002, 67, 8901-8905.
    • (2002) J. Org. Chem. , vol.67 , pp. 8901-8905
    • Du, Y.1    Lu, X.2    Yu, Y.3
  • 65
    • 0030919677 scopus 로고    scopus 로고
    • Phosphine-catalyzed [3+2] cycloaddition reaction of methyl 2,3-butadienoate and N-tosylimines. A novel approach to nitrogen heterocycles
    • L Xu, Z.; Lu, X. Phosphine-catalyzed [3+2] cycloaddition reaction of methyl 2,3-butadienoate and N-tosylimines. A novel approach to nitrogen heterocycles. Tetrahedron Lett., 1997, 38, 3461-3464.
    • (1997) Tetrahedron Lett , vol.38 , pp. 3461-3464
    • L Xu, Z.1    Lu, X.2
  • 66
    • 0000182934 scopus 로고    scopus 로고
    • A novel [3+2] cycloaddition approach to nitrogen heterocycles via phosphine-catalyzed reactions of 2,3-butadienoates or 2-butynoates and dimethyl acetylenedicarboxylate with imines: A convenient synthesis of pentabromopseudilin
    • Xu, Z.; Lu, X. A novel [3+2] cycloaddition approach to nitrogen heterocycles via phosphine-catalyzed reactions of 2,3-butadienoates or 2-butynoates and dimethyl acetylenedicarboxylate with imines: A convenient synthesis of pentabromopseudilin. J. Org. Chem., 1998, 63, 5031-5041.
    • (1998) J. Org. Chem. , vol.63 , pp. 5031-5041
    • Xu, Z.1    Lu, X.2
  • 67
    • 0030974493 scopus 로고    scopus 로고
    • Asymmetric [3+2] cycloaddition of 2,3-butadienoates with electron-deficient olefins catalyzed by novel chiral 2,5-dialkyl-7-phenyl-7-phosphabicyclo[2.2.1]heptanes
    • Zhu, G.; Chen. Z.; Jiang, Q.; Xiao, D.; Cao, P.; Zhang, X. Asymmetric [3+2] cycloaddition of 2,3-butadienoates with electron-deficient olefins catalyzed by novel chiral 2,5-dialkyl-7-phenyl-7-phosphabicyclo[2.2.1]heptanes. J. Am. Chem. Soc., 1997, 119, 3836-3837.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 3836-3837
    • Zhu, G.1    Chen, Z.2    Jiang, Q.3    Xiao, D.4    Cao, P.5    Zhang, X.6
  • 68
    • 0028288493 scopus 로고
    • Novel atropisomeric phosphorus ligands: 4,5-dihydro-3H-dinaphtho[2,1-c;1',2'-e]phosphepine derivatives
    • Gladiali, S.; Dore, A.; Fabbri, D.; De Lucchi, O.; Manassero, M. Novel atropisomeric phosphorus ligands: 4,5-dihydro-3H-dinaphtho[2,1-c;1',2'-e]phosphepine derivatives. Tetrahedron: Asymmetry, 1994, 5, 511-514.
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 511-514
    • Gladiali, S.1    Dore, A.2    Fabbri, D.3    de Lucchi, O.4    Manassero, M.5
  • 69
    • 33745941049 scopus 로고    scopus 로고
    • Synthesis of functionalized cyclopentenes through catalytic asymmetric [3+2] cycloadditions of allenes with enones
    • Wilson, J. E.; Fu, G. C. Synthesis of functionalized cyclopentenes through catalytic asymmetric [3+2] cycloadditions of allenes with enones. Angew. Chem. Int. Ed., 2006, 45, 1426-1429.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1426-1429
    • Wilson, J.E.1    Fu, G.C.2
  • 70
    • 33344475774 scopus 로고    scopus 로고
    • Phosphine-catalyzed enantioselective [3+2] annulations of 2,3-butadienoates with imines
    • Jean, L.; Marinetti, A. Phosphine-catalyzed enantioselective [3+2] annulations of 2,3-butadienoates with imines. Tetrahedron Lett., 2006, 47, 2141-2145.
    • (2006) Tetrahedron Lett , vol.47 , pp. 2141-2145
    • Jean, L.1    Marinetti, A.2
  • 71
    • 35348877267 scopus 로고    scopus 로고
    • Screening of chiral phosphines as catalysts for the enantioselective [3+2] annulations of N-tosylimines with allenic esters
    • Fleury-Brégeot, N.; Jean, L.; Retailleau, P.; Marinetti, A. Screening of chiral phosphines as catalysts for the enantioselective [3+2] annulations of N-tosylimines with allenic esters. Tetrahedron, 2007, 63, 11920-11927.
    • (2007) Tetrahedron , vol.63 , pp. 11920-11927
    • Fleury-Brégeot, N.1    Jean, L.2    Retailleau, P.3    Marinetti, A.4
  • 73
    • 33846917246 scopus 로고    scopus 로고
    • Phosphine-catalyzed cycloadditions of allenic ketones: New substrates for nucleophilic catalysis
    • Wallace, D. J.; Sidda, R. L.; Reamer, R. A. Phosphine-catalyzed cycloadditions of allenic ketones: New substrates for nucleophilic catalysis J. Org. Chem., 2007, 72, 1051-1054.
    • (2007) J. Org. Chem. , vol.72 , pp. 1051-1054
    • Wallace, D.J.1    Sidda, R.L.2    Reamer, R.A.3
  • 74
    • 34548756763 scopus 로고    scopus 로고
    • Enantioselective [3+2]-cycloadditions catalyzed by a protected, multifunctional phosphine-containing α-amino acid
    • Cowen, B. J.; Miller, S. J. Enantioselective [3+2]-cycloadditions catalyzed by a protected, multifunctional phosphine-containing α-amino acid. J. Am. Chem. Soc., 2007, 129, 10988-10989.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 10988-10989
    • Cowen, B.J.1    Miller, S.J.2
  • 75
    • 42649130688 scopus 로고    scopus 로고
    • Cooperative, highly enantioselective phosphinothiourea catalysis of imine-allene [3+2] cycloadditions
    • Fang, Y.-Q.; Jacobsen, E. N. Cooperative, highly enantioselective phosphinothiourea catalysis of imine-allene [3+2] cycloadditions. J. Am. Chem. Soc., 2008, 130, 5660-5661.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 5660-5661
    • Fang, Y.-Q.1    Jacobsen, E.N.2
  • 76
    • 54849416798 scopus 로고    scopus 로고
    • 2-Phospha[3]ferrocenophanes with planar chirality: Synthesis and use in enantioselective organocatalytic [3+2] cyclizations
    • Voituriez, A.; Panossian, A.; Fleury-Brégeot, N.; Retailleau, P.; Marinetti, A. 2-Phospha[3]ferrocenophanes with planar chirality: Synthesis and use in enantioselective organocatalytic [3+2] cyclizations. J. Am. Chem. Soc., 2008, 130, 14030-14031.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 14030-14031
    • Voituriez, A.1    Panossian, A.2    Fleury-Brégeot, N.3    Retailleau, P.4    Marinetti, A.5
  • 77
    • 68949130173 scopus 로고    scopus 로고
    • Synthesis of chiral 2-phospha[3]ferrocenophanes and their behaviour as organocatalysts in [3+2] cyclization reactions
    • Voituriez, A.; Panossian, A.; Fleeury-Brégeot, N.; Retailleau, P.; Marinetti, A. Synthesis of chiral 2-phospha[3]ferrocenophanes and their behaviour as organocatalysts in [3+2] cyclization reactions. Adv. Synth. Catal., 2009, 351, 1968-1976.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 1968-1976
    • Voituriez, A.1    Panossian, A.2    Fleeury-Brégeot, N.3    Retailleau, P.4    Marinetti, A.5
  • 78
    • 53749090597 scopus 로고    scopus 로고
    • Use of allenylphosphonates as new substrates for phosphane-catalyzed [3+2] and [4+2] annulations
    • Panossian, A.; Fleury-Brégeot, N.; Marinetti, A. Use of allenylphosphonates as new substrates for phosphane-catalyzed [3+2] and [4+2] annulations. Eur. J. Org. Chem., 2008, 3826-3833.
    • (2008) Eur. J. Org. Chem. , pp. 3826-3833
    • Panossian, A.1    Fleury-Brégeot, N.2    Marinetti, A.3
  • 79
    • 58649118228 scopus 로고    scopus 로고
    • Enantioselective binaphthophosphepine-promoted [3+2] annulations of N-Ts and N-DPPimines with allenoates and 2-butynoates
    • Pinto, N.; Fleury-Brégeot, N.; Marinetti, A. Enantioselective binaphthophosphepine-promoted [3+2] annulations of N-Ts and N-DPPimines with allenoates and 2-butynoates. Eur. J. Org. Chem., 2009, 146-151.
    • (2009) Eur. J. Org. Chem. , pp. 146-151
    • Pinto, N.1    Fleury-Brégeot, N.2    Marinetti, A.3
  • 80
    • 0037462076 scopus 로고    scopus 로고
    • An expedient phosphine-catalyzed [4+2] annulation: Synthesis of highly functionalized tetrahydropyridines
    • Zhu, X.-F.; Lan, J.; Kwon, O. An expedient phosphine-catalyzed [4+2] annulation: Synthesis of highly functionalized tetrahydropyridines. J. Am. Chem. Soc., 2003, 125, 4716-4717.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4716-4717
    • Zhu, X.-F.1    Lan, J.2    Kwon, O.3
  • 81
    • 24644437269 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of piperidine derivatives through the [4+2] annulation of imines with allenes
    • Wurz, R. P.; Fu, G. C. Catalytic asymmetric synthesis of piperidine derivatives through the [4+2] annulation of imines with allenes J. Am. Chem. Soc., 2005, 127, 12234-12235.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 12234-12235
    • Wurz, R.P.1    Fu, G.C.2
  • 82
    • 84989832417 scopus 로고
    • Novel umpolung in C-C bond formation catalyzed by triphenylphosphine
    • Trost, B. M.; Li, C.-J. Novel umpolung in C-C bond formation catalyzed by triphenylphosphine. J. Am. Chem. Soc., 1994, 116, 3167-3168.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 3167-3168
    • Trost, B.M.1    Li, C.-J.2
  • 83
    • 0011223739 scopus 로고    scopus 로고
    • Asymmetric formation of quaternary carbon centers catalyzed by novel chiral 2,5-dialkyl-7-phenyl-7-phosphabicyclo[2.2.1]heptanes
    • Chen, Z.; Zhu, G.; Jiang, Q.; Xiao, D.; Cao, P.; Zhang, X. Asymmetric formation of quaternary carbon centers catalyzed by novel chiral 2,5-dialkyl-7-phenyl-7-phosphabicyclo[2.2.1]heptanes. J. Org. Chem., 1998, 63, 5631-5635.
    • (1998) J. Org. Chem. , vol.63 , pp. 5631-5635
    • Chen, Z.1    Zhu, G.2    Jiang, Q.3    Xiao, D.4    Cao, P.5    Zhang, X.6
  • 84
    • 0001563584 scopus 로고
    • Phosphine-catalyzed isomerization-addition of oxygen nucleophiles to 2-alkynoates
    • Trost, B. M.; Li, C.-J. Phosphine-catalyzed isomerization-addition of oxygen nucleophiles to 2-alkynoates. J. Am. Chem. Soc., 1994, 116, 10819-10820.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 10819-10820
    • Trost, B.M.1    Li, C.-J.2
  • 85
    • 61949284410 scopus 로고    scopus 로고
    • Phosphine-catalyzed enantioselective synthesis of oxygen heterocycles
    • Chung, Y. K.; Fu, G. C. Phosphine-catalyzed enantioselective synthesis of oxygen heterocycles Angew. Chem. Int. Ed., 2009, 48, 2225-2227.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 2225-2227
    • Chung, Y.K.1    Fu, G.C.2
  • 86
    • 0002842478 scopus 로고
    • Über eine einfache darstellung von acyloxazolinonen-(5) aus 5-acyloxy-oxazolen II. Mitteilung über hypernucleophile acylierungskatalysatoren
    • Steglich, W.; Höfle, G. Über eine einfache darstellung von acyloxazolinonen-(5) aus 5-acyloxy-oxazolen II. Mitteilung über hypernucleophile acylierungskatalysatoren. Tetrahedron Lett., 1970, 11, 4727-4730.
    • (1970) Tetrahedron Lett , vol.11 , pp. 4727-4730
    • Steglich, W.1    Höfle, G.2
  • 87
    • 0032508967 scopus 로고    scopus 로고
    • Enantioselective construction of quaternary stereocenters: Rearrangements of O-acylated azlactones catalyzed by a planar-chiral derivative of 4-(pyrrolidino)pyridine
    • Ruble, J. G.; Fu, G. C. Enantioselective construction of quaternary stereocenters: Rearrangements of O-acylated azlactones catalyzed by a planar-chiral derivative of 4-(pyrrolidino)pyridine. J. Am. Chem. Soc., 1998, 120, 11532-11533.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 11532-11533
    • Ruble, J.G.1    Fu, G.C.2
  • 88
    • 0242330806 scopus 로고    scopus 로고
    • Development of chiral nucleophilic pyridine catalysts: Applications in asymmetric quaternary carbon synthesis
    • Shaw, S.; Aleman, P.; Vedejs, E. Development of chiral nucleophilic pyridine catalysts: Applications in asymmetric quaternary carbon synthesis. J. Am. Chem. Soc., 2003, 125, 13368-13369.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 13368-13369
    • Shaw, S.1    Aleman, P.2    Vedejs, E.3
  • 89
    • 85196433409 scopus 로고    scopus 로고
    • For the synthesis and application of enantiopure alcohols, see
    • For the synthesis and application of enantiopure alcohols, see
  • 92
    • 0000149447 scopus 로고
    • Cyclohexyl-based chiral auxiliaries
    • Whitesell, J. K. Cyclohexyl-based chiral auxiliaries. Chem. Rev., 1992, 92, 953-964.
    • (1992) Chem. Rev. , vol.92 , pp. 953-964
    • Whitesell, J.K.1
  • 94
    • 0000085691 scopus 로고    scopus 로고
    • Biotransformations in the synthesis of enantiopure bioactive molecules
    • Johnson, C. R. Biotransformations in the synthesis of enantiopure bioactive molecules. Acc. Chem. Res., 1998, 31, 333-341.
    • (1998) Acc. Chem. Res. , vol.31 , pp. 333-341
    • Johnson, C.R.1
  • 95
    • 80051729483 scopus 로고
    • Tributylphosphine: A remarkable acylation catalyst
    • Vedejs, E.; Diver, S. T. Tributylphosphine: A remarkable acylation catalyst. J. Am. Chem. Soc., 1993, 115, 3358-3359.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 3358-3359
    • Vedejs, E.1    Diver, S.T.2
  • 97
    • 0001526323 scopus 로고    scopus 로고
    • Enantioselective acylations catalyzed by chiral phosphines
    • Vedejs, E.; Daugulis, O.; Diver, S. T. Enantioselective acylations catalyzed by chiral phosphines. J. Org. Chem., 1996, 61, 430-431.
    • (1996) J. Org. Chem. , vol.61 , pp. 430-431
    • Vedejs, E.1    Daugulis, O.2    Diver, S.T.3
  • 98
    • 0037534410 scopus 로고    scopus 로고
    • A comparison of monocyclic and bicyclic phospholanes as acyl-transfer catalysts
    • Vedejs, E.; Daugulis, O.; Harper, L. A.; Mackay, J. A.; PoWell, D. R. A comparison of monocyclic and bicyclic phospholanes as acyl-transfer catalysts. J. Org. Chem., 2003, 68, 5020-5027.
    • (2003) J. Org. Chem. , vol.68 , pp. 5020-5027
    • Vedejs, E.1    Daugulis, O.2    Harper, L.A.3    Mackay, J.A.4    Powell, D.R.5
  • 99
    • 0033597606 scopus 로고    scopus 로고
    • 2-Aryl-4,4,8-trimethyl-2-phosphabicyclo[3.3.0]octanes: Reactive chiral phosphine catalysts for enantioselective acylation
    • Vedejs, E.; Daugulis, O. 2-Aryl-4,4,8-trimethyl-2-phosphabicyclo[3.3.0]octanes: Reactive chiral phosphine catalysts for enantioselective acylation. J. Am. Chem. Soc., 1999, 121, 5813-5814.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 5813-5814
    • Vedejs, E.1    Daugulis, O.2
  • 100
    • 0242500932 scopus 로고    scopus 로고
    • A highly enantioselective phosphabicyclooctane catalyst for the kinetic resolution of benzylic alcohols
    • Vedejs, E.; Daugulis, O. A highly enantioselective phosphabicyclooctane catalyst for the kinetic resolution of benzylic alcohols. J. Am. Chem. Soc., 2003, 125, 4166-4173.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4166-4173
    • Vedejs, E.1    Daugulis, O.2
  • 101
    • 0000363155 scopus 로고    scopus 로고
    • Kinetic resolution of allylic alcohols using a chiral phosphine catalyst
    • Vedejs, E.; Mackay, J. A. Kinetic resolution of allylic alcohols using a chiral phosphine catalyst. Org. Lett., 2001, 3, 535-536.
    • (2001) Org. Lett. , vol.3 , pp. 535-536
    • Vedejs, E.1    Mackay, J.A.2
  • 102
    • 0034802190 scopus 로고    scopus 로고
    • Parallel kinetic resolution under catalytic conditions: A three-phase system allows selective reagent activation using two catalysts
    • Vedejs, E.; Rozners, E. Parallel kinetic resolution under catalytic conditions: A three-phase system allows selective reagent activation using two catalysts. J. Am. Chem. Soc., 2001, 123, 2428-2429.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 2428-2429
    • Vedejs, E.1    Rozners, E.2
  • 103
    • 2542448981 scopus 로고    scopus 로고
    • Phosphine-catalyzed regiospecific allylic amination and dynamic kinetic resolution of Morita-Baylis-Hillman acetates
    • Cho, C.-W.; Kong, J.-R.; Krische, M. J. Phosphine-catalyzed regiospecific allylic amination and dynamic kinetic resolution of Morita-Baylis-Hillman acetates. Org. Lett., 2004, 6, 1337-1339.
    • (2004) Org. Lett. , vol.6 , pp. 1337-1339
    • Cho, C.-W.1    Kong, J.-R.2    Krische, M.J.3
  • 104
    • 34548530713 scopus 로고    scopus 로고
    • Enantioselective allylic substitution of Morita-Baylis-Hillman adducts catalyzed by planar chiral [2.2]paracyclophane monophosphines
    • Zhang, T.-Z.; Dai, L.-X.; Hou, X.-L. Enantioselective allylic substitution of Morita-Baylis-Hillman adducts catalyzed by planar chiral [2.2]paracyclophane monophosphines. Tetrahedron: Asymmetry, 2007, 18, 1990-1994.
    • (2007) Tetrahedron: Asymmetry , vol.18 , pp. 1990-1994
    • Zhang, T.-Z.1    Dai, L.-X.2    Hou, X.-L.3
  • 105
    • 65549153573 scopus 로고    scopus 로고
    • Chiral phosphine-catalyzed regio- and enantioselective allylic amination of Morita-Baylis-Hillman acetates
    • Ma, G.-N.; Cao, S.-H.; Shi, M. Chiral phosphine-catalyzed regio- and enantioselective allylic amination of Morita-Baylis-Hillman acetates. Tetrahedron: Asymmetry, 2009, 20, 1086-1092.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1086-1092
    • Ma, G.-N.1    Cao, S.-H.2    Shi, M.3
  • 106
    • 85196433529 scopus 로고    scopus 로고
    • Selected reviews on the synthesis of γ-butenolides
    • Selected reviews on the synthesis of γ-butenolides
  • 107
    • 33846471698 scopus 로고    scopus 로고
    • Synthesis of butenolides by one-Pot cyclization reactions of silyl enol ethers with oxalyl chloride
    • Langer, P. Synthesis of butenolides by one-Pot cyclization reactions of silyl enol ethers with oxalyl chloride. Synlett, 2006, 3369-3381.
    • (2006) Synlett , pp. 3369-3381
    • Langer, P.1
  • 108
    • 33646082198 scopus 로고    scopus 로고
    • CAlkoxycarbonyl nitrones: Building blocks for the synthesis of butenolides, lactams and modified nucleosides
    • Romeo, G.; Iannazzo, D.; Piperno, A.; Romeo, R.; Corsaro, A.; Rescifina, A.; Chiacchio, U. CAlkoxycarbonyl nitrones: Building blocks for the synthesis of butenolides, lactams and modified nucleosides. Mini-Rev. Org. Chem., 2005, 2, 59-77.
    • (2005) Mini-Rev. Org. Chem. , vol.2 , pp. 59-77
    • Romeo, G.1    Iannazzo, D.2    Piperno, A.3    Romeo, R.4    Corsaro, A.5    Rescifina, A.6    Chiacchio, U.7
  • 109
    • 0034974653 scopus 로고    scopus 로고
    • The synthesis of γ-alkylidenebutenolides
    • Bruckner, R. The synthesis of γ-alkylidenebutenolides. Curr. Org. Chem., 2001, 5, 679-718.
    • (2001) Curr. Org. Chem. , vol.5 , pp. 679-718
    • Bruckner, R.1
  • 110
    • 44949204654 scopus 로고    scopus 로고
    • Chiral phosphine-catalyzed enantioselective construction of γ-butenolides through substitution of Morita-Baylis-Hillman acetates with 2-trimethylsilyloxy furan
    • Jiang, Y.-Q.; Shi, Y.-L.; Shi, M. Chiral phosphine-catalyzed enantioselective construction of γ-butenolides through substitution of Morita-Baylis-Hillman acetates with 2-trimethylsilyloxy furan. J. Am. Chem. Soc., 2008, 130, 7202-7203.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 7202-7203
    • Jiang, Y.-Q.1    Shi, Y.-L.2    Shi, M.3
  • 111
    • 1242307308 scopus 로고    scopus 로고
    • Desymmetrization of meso-hydrobenzoin using chiral, nucleophilic phosphine Catalysts
    • Vedejs, E.; Daugulis, O.; Tuttle, N. Desymmetrization of meso-hydrobenzoin using chiral, nucleophilic phosphine Catalysts. J. Org. Chem., 2004, 69, 1389-1392.
    • (2004) J. Org. Chem. , vol.69 , pp. 1389-1392
    • Vedejs, E.1    Daugulis, O.2    Tuttle, N.3
  • 112
    • 67649336812 scopus 로고    scopus 로고
    • Bifunctional Asymmetric catalysis with hydrogen chloride: Enantioselective ring opening of aziridines catalyzed by a phosphinothiourea
    • Mita, T.; Jacobsen, E. N. Bifunctional Asymmetric catalysis with hydrogen chloride: enantioselective ring opening of aziridines catalyzed by a phosphinothiourea. Synlett, 2009, 1680-1684.
    • (2009) Synlett , pp. 1680-1684
    • Mita, T.1    Jacobsen, E.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.