메뉴 건너뛰기




Volumn , Issue , 2011, Pages 625-670

Recent Advances in the Metal-Catalyzed Stereoselective Synthesis of Biologically Active Molecules

Author keywords

Asymmetric cycloadditions, and Diels Alder reaction (DA) asymmetric DA reactions, Lewis acids accelerating cycloaddition; Enantioselective oxidations alkene oxidations, hydrogenations and cyclopropanations; Recent advances, metal catalyzed stereoselective synthesis asymmetric organometallic reactions

Indexed keywords


EID: 84886041418     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781118087992.ch15     Document Type: Chapter
Times cited : (3)

References (142)
  • 1
    • 49949143547 scopus 로고
    • Asymmetric induction in carbenoid reactions by means of a dissymmetric copper chelate
    • Nozaki, H., Moriuti, S., Takaya, H., Noyori, R. (1966). Asymmetric induction in carbenoid reactions by means of a dissymmetric copper chelate. Tetrahedron Lett., 43, 5239-5244.
    • (1966) Tetrahedron Lett., , vol.43 , pp. 5239-5244
    • Nozaki, H.1    Moriuti, S.2    Takaya, H.3    Noyori, R.4
  • 5
    • 72149111935 scopus 로고    scopus 로고
    • Mechanism of enantioselection in Rh-catalyzed asymmetric hydrogenation. The origin of utmost catalytic performance
    • Recent reviews: (a) Gridnev, I. D., Imamoto, T. (2009). Mechanism of enantioselection in Rh-catalyzed asymmetric hydrogenation. The origin of utmost catalytic performance. Chem. Commun., 48, 7447-7464
    • (2009) Chem. Commun , vol.48 , pp. 7447-7464
    • Gridnev, I.D.1    Imamoto, T.2
  • 6
    • 0033918708 scopus 로고    scopus 로고
    • Modular phospholane ligands in asymmetric catalysis
    • Burk, M. J. (2000). Modular phospholane ligands in asymmetric catalysis . Acc. Chem. Res., 33, 363-372.
    • (2000) Acc. Chem. Res., , vol.33 , pp. 363-372
    • Burk, M.J.1
  • 9
    • 38549124342 scopus 로고    scopus 로고
    • Eight-step total synthesis of the cyclopeptide alkaloid Mucronine E
    • Toumi, M., Couty, F., Evano, G. (2008). Eight-step total synthesis of the cyclopeptide alkaloid Mucronine E. Synlett., 29-32.
    • (2008) Synlett., , pp. 29-32
    • Toumi, M.1    Couty, F.2    Evano, G.3
  • 10
    • 45549085402 scopus 로고    scopus 로고
    • Formal total synthesis of (-)-Haouamine A
    • Fürstner, A., Ackerstaff, J. (2008). Formal total synthesis of (-)-Haouamine A. Chem. Commun., 2870-2872.
    • (2008) Chem. Commun., , pp. 2870-2872
    • Fürstner, A.1    Ackerstaff, J.2
  • 11
    • 77950202999 scopus 로고    scopus 로고
    • Phosphoramidites: privileged ligands in asymmetric catalysis
    • Teichert, J. F., Feringa, B. L. (2010). Phosphoramidites: privileged ligands in asymmetric catalysis . Angew. Chem., Int. Ed., 49, 2486-2528.
    • (2010) Angew. Chem., Int. Ed., , vol.49 , pp. 2486-2528
    • Teichert, J.F.1    Feringa, B.L.2
  • 12
    • 38049033351 scopus 로고    scopus 로고
    • Asymmetric hydrogenation using monodentate phosphoramidite ligands
    • Minnaard, A. J., Feringa, B. L., Lefort, L., de Vries, J. G. (2007). Asymmetric hydrogenation using monodentate phosphoramidite ligands. Acc. Chem. Res., 40, 1267-1277.
    • (2007) Acc. Chem. Res., , vol.40 , pp. 1267-1277
    • Minnaard, A.J.1    Feringa, B.L.2    Lefort, L.3    de Vries, J.G.4
  • 13
    • 38049062016 scopus 로고    scopus 로고
    • A mixed-ligand approach enables the asymmetric hydrogenation of an a-isopropylcinnamic acid en route to the renin inhibitor aliskiren
    • Boogers, J. A. F., Felfer, U., Kotthaus, M., Lefort, L., Steinbauer, G., De Vries, A. H. M., De Vries, J. G. A. (2007). A mixed-ligand approach enables the asymmetric hydrogenation of an a-isopropylcinnamic acid en route to the renin inhibitor aliskiren. O rg. Process Res. Dev., 11, 585-591.
    • (2007) O rg. Process Res. Dev., , vol.11 , pp. 585-591
    • Boogers, J.A.F.1    Felfer, U.2    Kotthaus, M.3    Lefort, L.4    Steinbauer, G.5    De Vries, A.H.M.6    De Vries, J.G.A.7
  • 14
    • 0002123299 scopus 로고    scopus 로고
    • Asymmetric transfer hydrogenation catalyzed by chiral ruthenium complexes
    • Noyori, R., Hashiguchi, S. (1997). Asymmetric transfer hydrogenation catalyzed by chiral ruthenium complexes . Acc. Chem. Res., 30, 97-102.
    • (1997) Acc. Chem. Res., , vol.30 , pp. 97-102
    • Noyori, R.1    Hashiguchi, S.2
  • 15
    • 0030883527 scopus 로고    scopus 로고
    • Asymmetric transfer hydrogenation of a, ß-acetylenic ketones
    • Matsumura, K., Hashiguchi, S., Ikariya, T., Noyori, R. (1997). Asymmetric transfer hydrogenation of a, ß-acetylenic ketones . J. Am. Chem. Soc., 119, 8738-8739.
    • (1997) J. Am. Chem. Soc., , vol.119 , pp. 8738-8739
    • Matsumura, K.1    Hashiguchi, S.2    Ikariya, T.3    Noyori, R.4
  • 17
    • 57149084689 scopus 로고    scopus 로고
    • Total synthesis of (-)-Pseudolaric acid B
    • Trost, B. M., Waser, J., Meyer, A. (2008). Total synthesis of (-)-Pseudolaric acid B . J. Am. Chem. Soc., 130, 16424-16434.
    • (2008) J. Am. Chem. Soc., , vol.130 , pp. 16424-16434
    • Trost, B.M.1    Waser, J.2    Meyer, A.3
  • 18
    • 36749001573 scopus 로고    scopus 로고
    • Total synthesis of (-)-Pseudolaric acid B
    • Trost, B. M., Waser, J., Meyer, A. (2007). Total synthesis of (-)-Pseudolaric acid B. J. Am. Chem. Soc., 129, 14556-14557.
    • (2007) J. Am. Chem. Soc., , vol.129 , pp. 14556-14557
    • Trost, B.M.1    Waser, J.2    Meyer, A.3
  • 21
    • 34547467855 scopus 로고    scopus 로고
    • Total synthesis of Iejimalide A-D and assessment of the remarkable actin-depolymerizing capacity of these polyene macrolides
    • Fürstner, A., Nevado, C., Waser, M., Tremblay, M., Chevrier, C., Teply, F., Aïssa, C., Moulin, E., Müller, O. (2007). Total synthesis of Iejimalide A-D and assessment of the remarkable actin-depolymerizing capacity of these polyene macrolides. J. Am. Chem. Soc., 129, 9150-9161.
    • (2007) J. Am. Chem. Soc., , vol.129 , pp. 9150-9161
    • Fürstner, A.1    Nevado, C.2    Waser, M.3    Tremblay, M.4    Chevrier, C.5    Teply, F.6    Aïssa, C.7    Moulin, E.8    Müller, O.9
  • 22
    • 39749098365 scopus 로고    scopus 로고
    • Improved total synthesis of the potent HDAC inhibitor FK228 (FR-901228)
    • Greshock, T. J., Johns, D. M., Noguchi, Y., Williams, R. M. (2008). Improved total synthesis of the potent HDAC inhibitor FK228 (FR-901228). Org. Lett., 10, 613-616.
    • (2008) Org. Lett., , vol.10 , pp. 613-616
    • Greshock, T.J.1    Johns, D.M.2    Noguchi, Y.3    Williams, R.M.4
  • 23
    • 37549071843 scopus 로고    scopus 로고
    • Asymmetric synthesis and biological properties of Uncialamycin and 26-epi-uncialamycin
    • Nicolaou, K. C., Chen, J. S., Zhang, H., Montero, A. (2008). Asymmetric synthesis and biological properties of Uncialamycin and 26-epi-uncialamycin. Angew. Chem. Int. Ed., 47, 185-189.
    • (2008) Angew. Chem. Int. Ed., , vol.47 , pp. 185-189
    • Nicolaou, K.C.1    Chen, J.S.2    Zhang, H.3    Montero, A.4
  • 24
    • 72249094956 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (-)-(S)-Stepholidine
    • Cheng, J., Yang, Y. (2009). Enantioselective total synthesis of (-)-(S)-Stepholidine. J. Org. Chem., 74, 9225-9228.
    • (2009) J. Org. Chem., , vol.74 , pp. 9225-9228
    • Cheng, J.1    Yang, Y.2
  • 25
    • 18844410382 scopus 로고
    • Catalytic asymmetric epoxidation and kinetic resolution: modifi ed procedures including in situ derivatization
    • Gao, Y., Klunder, J. M., Hanson, R. M., Masamune, H., Ko, S. Y., Sharpless, K. B. (1987). Catalytic asymmetric epoxidation and kinetic resolution: modifi ed procedures including in situ derivatization . J. Am. Chem. Soc., 109, 5765-5780.
    • (1987) J. Am. Chem. Soc., , vol.109 , pp. 5765-5780
    • Gao, Y.1    Klunder, J.M.2    Hanson, R.M.3    Masamune, H.4    Ko, S.Y.5    Sharpless, K.B.6
  • 27
    • 0000016656 scopus 로고
    • Selective asymmetric dihydroxylation (AD) of dienes
    • Xu, D., Crispino, G. A., Sharpless, K. B. (1992). Selective asymmetric dihydroxylation (AD) of dienes . J. Am. Chem. Soc., 114, 7570-7571.
    • (1992) J. Am. Chem. Soc., , vol.114 , pp. 7570-7571
    • Xu, D.1    Crispino, G.A.2    Sharpless, K.B.3
  • 28
    • 0000797769 scopus 로고
    • Catalytic asymmetric dihydroxylation of cis-disubstituted olefi ns
    • Wang, L., Sharpless, K. B. (1992). Catalytic asymmetric dihydroxylation of cis-disubstituted olefi ns. J. Am. Chem. Soc., 114, 7568-7570.
    • (1992) J. Am. Chem. Soc., , vol.114 , pp. 7568-7570
    • Wang, L.1    Sharpless, K.B.2
  • 29
    • 77649204480 scopus 로고    scopus 로고
    • Synthetic applications of chiral unsaturated epoxy alcohols prepared by Sharpless asymmetric epoxidation
    • Riera, A., Moreno, M. (2010). Synthetic applications of chiral unsaturated epoxy alcohols prepared by Sharpless asymmetric epoxidation. Molecules, 15, 1041-1073.
    • (2010) Molecules, , vol.15 , pp. 1041-1073
    • Riera, A.1    Moreno, M.2
  • 31
    • 61349164707 scopus 로고    scopus 로고
    • Asymmetric dihydroxylation of alkenes
    • Noe, M. C., Letavic, M. A., Snow, S. L. (2005). Asymmetric dihydroxylation of alkenes . Org. React., 66, 109-625.
    • (2005) Org. React., , vol.66 , pp. 109-625
    • Noe, M.C.1    Letavic, M.A.2    Snow, S.L.3
  • 32
    • 32144460995 scopus 로고    scopus 로고
    • Total synthesis and revision of C6 stereochemistry of (+)-Amphidinolide W
    • Ghosh, A. K., Gong, G. (2006). Total synthesis and revision of C6 stereochemistry of (+)-Amphidinolide W. J. Org. Chem., 71, 1085-1093.
    • (2006) J. Org. Chem., , vol.71 , pp. 1085-1093
    • Ghosh, A.K.1    Gong, G.2
  • 33
    • 1842789167 scopus 로고    scopus 로고
    • An experimentally derived model for stereoselectivity in the aerobic oxidative kinetic resolution of secondary alcohols by (sparteine)PdCl 2
    • Trend, R. M., Stoltz, B. M. (2004). An experimentally derived model for stereoselectivity in the aerobic oxidative kinetic resolution of secondary alcohols by (sparteine)PdCl 2 . J. Am. Chem. Soc., 126, 4482-4483.
    • (2004) J. Am. Chem. Soc., , vol.126 , pp. 4482-4483
    • Trend, R.M.1    Stoltz, B.M.2
  • 34
    • 0034823071 scopus 로고    scopus 로고
    • Palladium-catalyzed enantioselective oxidations of alcohols using molecular oxygen
    • Jensen, D. R., Pugsley, J. S., Sigman, M. S. (2001). Palladium-catalyzed enantioselective oxidations of alcohols using molecular oxygen. J. Am. Chem. Soc., 123, 7475-7476.
    • (2001) J. Am. Chem. Soc., , vol.123 , pp. 7475-7476
    • Jensen, D.R.1    Pugsley, J.S.2    Sigman, M.S.3
  • 35
    • 53849126527 scopus 로고    scopus 로고
    • Pd-catalyzed enantioselective aerobic oxidation of secondary alcohols: applications to the total synthesis of alkaloids
    • Krishnan, S., Bagdanoff, J. T., Ebner, D. C., Ramtohul, Y. K., Tambar, U. K., Stoltz, B. M. (2008). Pd-catalyzed enantioselective aerobic oxidation of secondary alcohols: applications to the total synthesis of alkaloids. J. Am. Chem. Soc., 130, 13745-13754.
    • (2008) J. Am. Chem. Soc., , vol.130 , pp. 13745-13754
    • Krishnan, S.1    Bagdanoff, J.T.2    Ebner, D.C.3    Ramtohul, Y.K.4    Tambar, U.K.5    Stoltz, B.M.6
  • 36
    • 40949131811 scopus 로고    scopus 로고
    • Enantioselective synthesis of bicyclo[2.2.2]octenones using a copper-mediated oxidative dearomatization/ [4 + 2] dimerization cascade
    • Dong, S., Zhu, J., Porco, J. A., Jr. (2008). Enantioselective synthesis of bicyclo[2.2.2]octenones using a copper-mediated oxidative dearomatization/ [4 + 2] dimerization cascade . J. Am. Chem. Soc., 130, 2738-2739.
    • (2008) J. Am. Chem. Soc., , vol.130 , pp. 2738-2739
    • Dong, S.1    Zhu, J.2    Porco Jr., J.A.3
  • 37
    • 21644436580 scopus 로고    scopus 로고
    • Synthesis of the Azaphilones using copper-mediated enantioselective oxidative dearomatization
    • Zhu, J., Grigoriadis, N. P., Lee, J. P., Porco, J. A., Jr (2005). Synthesis of the Azaphilones using copper-mediated enantioselective oxidative dearomatization. J. Am. Chem. Soc., 127, 9342-9343.
    • (2005) J. Am. Chem. Soc., , vol.127 , pp. 9342-9343
    • Zhu, J.1    Grigoriadis, N.P.2    Lee, J.P.3    Porco Jr., J.A.4
  • 38
    • 34249006962 scopus 로고    scopus 로고
    • Total synthesis, assignment of absolute stereochemistry, and structural revision of Chlorofusin
    • Qian, W., Wei, W., Zhang, Y., Yao, Z. (2007). Total synthesis, assignment of absolute stereochemistry, and structural revision of Chlorofusin. J. Am. Chem. Soc., 129, 6400-6401.
    • (2007) J. Am. Chem. Soc., , vol.129 , pp. 6400-6401
    • Qian, W.1    Wei, W.2    Zhang, Y.3    Yao, Z.4
  • 41
    • 70349900286 scopus 로고    scopus 로고
    • Macrocyclization by nickel-catalyzed, ester-promoted, epoxide-alkyne reductive coupling: total synthesis of (-)-Gloeosporone
    • Trenkle, J. D., Jamison, T. F. (2009). Macrocyclization by nickel-catalyzed, ester-promoted, epoxide-alkyne reductive coupling: total synthesis of (-)-Gloeosporone. Angew. Chem. Int. Ed., 48, 5366-5368.
    • (2009) Angew. Chem. Int. Ed., , vol.48 , pp. 5366-5368
    • Trenkle, J.D.1    Jamison, T.F.2
  • 42
    • 0032507282 scopus 로고    scopus 로고
    • Lithium ephedrate-mediated addition of a lithium acetylide to a ketone: solution structures and relative reactivities of mixed aggregates underlying the high enantioselectivities
    • Thompson, A., Corley, E. G., Huntington, M. F., Grabowski, E. J. J., Remenar, J. F., Collum, D. B. (1998). Lithium ephedrate-mediated addition of a lithium acetylide to a ketone: solution structures and relative reactivities of mixed aggregates underlying the high enantioselectivities. J. Am. Chem. Soc., 120, 2028-2038.
    • (1998) J. Am. Chem. Soc., , vol.120 , pp. 2028-2038
    • Thompson, A.1    Corley, E.G.2    Huntington, M.F.3    Grabowski, E.J.J.4    Remenar, J.F.5    Collum, D.B.6
  • 43
    • 0041878778 scopus 로고    scopus 로고
    • Catalytic enantioselective addition of allylic organometallic reagents to aldehydes and ketones
    • Denmark, S. E., Fu, J. (2003). Catalytic enantioselective addition of allylic organometallic reagents to aldehydes and ketones. Chem. Rev., 103, 2763-2793.
    • (2003) Chem. Rev., , vol.103 , pp. 2763-2793
    • Denmark, S.E.1    Fu, J.2
  • 44
    • 0001488391 scopus 로고
    • Catalytic asymmetric allylation of aldehydes
    • Keck, G. E., Tarbet, K. H., Geraci, L. S. (1993). Catalytic asymmetric allylation of aldehydes. J. Am. Chem. Soc., 115, 8467-8468.
    • (1993) J. Am. Chem. Soc., , vol.115 , pp. 8467-8468
    • Keck, G.E.1    Tarbet, K.H.2    Geraci, L.S.3
  • 45
    • 43949108554 scopus 로고    scopus 로고
    • Asymmetric synthesis of (-)-Incarvillateine employing an intramolecular alkylation via Rh-catalyzed olefi nic C-H bond activation
    • Tsai, A. S., Bergman, R. G., Ellman, J. A. (2008). Asymmetric synthesis of (-)-Incarvillateine employing an intramolecular alkylation via Rh-catalyzed olefi nic C-H bond activation. J. Am. Chem. Soc., 130, 6316-6317.
    • (2008) J. Am. Chem. Soc., , vol.130 , pp. 6316-6317
    • Tsai, A.S.1    Bergman, R.G.2    Ellman, J.A.3
  • 46
    • 33646539473 scopus 로고    scopus 로고
    • Stereoselective alkylation of a, ß-unsaturated imines via C-H bond activation
    • Colby, D. A., Bergman, R. G., Ellman, J. A. (2006). Stereoselective alkylation of a, ß-unsaturated imines via C-H bond activation. J. Am. Chem. Soc., 128, 5604-5605.
    • (2006) J. Am. Chem. Soc., , vol.128 , pp. 5604-5605
    • Colby, D.A.1    Bergman, R.G.2    Ellman, J.A.3
  • 48
    • 0141757166 scopus 로고    scopus 로고
    • Catalytic asymmetric allylation of aldehydes and related reactions with bis[((S)-binaphthoxy) (isopropoxy)titanium] oxide as a micro-oxo-type chiral Lewis acid
    • Hanawa, H., Uraguchi, D., Konishi, S., Hashimoto, T., Maruoka, K. (2003). Catalytic asymmetric allylation of aldehydes and related reactions with bis[((S)-binaphthoxy) (isopropoxy)titanium] oxide as a micro-oxo-type chiral Lewis acid. C hem.-Eur. J., 9, 4405-4413.
    • (2003) C hem.-Eur. J., , vol.9 , pp. 4405-4413
    • Hanawa, H.1    Uraguchi, D.2    Konishi, S.3    Hashimoto, T.4    Maruoka, K.5
  • 49
    • 0029895814 scopus 로고    scopus 로고
    • Catalytic asymmetric allylation of aldehydes using a chiral silver(I) complex
    • Yanagisawa, A., Nakashima, H., Ishiba, A., Yamamoto, H. (1996). Catalytic asymmetric allylation of aldehydes using a chiral silver(I) complex. J. Am. Chem. Soc., 118, 4723-4724.
    • (1996) J. Am. Chem. Soc., , vol.118 , pp. 4723-4724
    • Yanagisawa, A.1    Nakashima, H.2    Ishiba, A.3    Yamamoto, H.4
  • 50
    • 36549045650 scopus 로고    scopus 로고
    • Reagent directing group controlled organic synthesis: total synthesis of (R,R,R)-(a)-Tocopherol
    • Rein, C., Demel, P., Outten, R. A., Netscher, T., Breit, B. (2007). Reagent directing group controlled organic synthesis: total synthesis of (R,R,R)-(a)-Tocopherol. Angew. Chem. Int. Ed., 46, 8670-8673.
    • (2007) Angew. Chem. Int. Ed., , vol.46 , pp. 8670-8673
    • Rein, C.1    Demel, P.2    Outten, R.A.3    Netscher, T.4    Breit, B.5
  • 51
    • 51049107936 scopus 로고    scopus 로고
    • Catalytic asymmetric conjugate addition and allylic alkylation with Grignard reagents
    • Harutyunyan, S. R., den Hartog, T., Geurts, K., Minnaard, A. J., Feringa, B. L. (2008). Catalytic asymmetric conjugate addition and allylic alkylation with Grignard reagents. Chem. Rev., 108, 2824-2852
    • (2008) Chem. Rev , vol.108 , pp. 2824-2852
    • Harutyunyan, S.R.1    den Hartog, T.2    Geurts, K.3    Minnaard, A.J.4    Feringa, B.L.5
  • 52
    • 0036793999 scopus 로고    scopus 로고
    • Enantioselective copper-catalyzed conjugate addition
    • Alexakis, A., Benhaim, C. (2002). Enantioselective copper-catalyzed conjugate addition . Eur. J. Org. Chem., 3221-3236.
    • (2002) Eur. J. Org. Chem., , pp. 3221-3236
    • Alexakis, A.1    Benhaim, C.2
  • 53
    • 68949109676 scopus 로고    scopus 로고
    • Synthesis of Iriomoteolide-1a C13-C23 fragment via asymmetric conjugate addition and Julia-Kocienski coupling reaction
    • Chin, Y., Wang, S., Loh, T. (2009). Synthesis of Iriomoteolide-1a C13-C23 fragment via asymmetric conjugate addition and Julia-Kocienski coupling reaction . Org. Lett., 11, 3674-3676.
    • (2009) Org. Lett., , vol.11 , pp. 3674-3676
    • Chin, Y.1    Wang, S.2    Loh, T.3
  • 54
    • 53549111870 scopus 로고    scopus 로고
    • Asymmetric total synthesis of PDIM A: a virulence factor of mycobacterium tuberculosis
    • Casas-Arce, E., Ter Horst, B., Feringa, B. L., Minnaard, A. J. (2008). Asymmetric total synthesis of PDIM A: a virulence factor of mycobacterium tuberculosis . Chem. Eur. J., 14, 4157-4159.
    • (2008) Chem. Eur. J., , vol.14 , pp. 4157-4159
    • Casas-Arce, E.1    Ter Horst, B.2    Feringa, B.L.3    Minnaard, A.J.4
  • 55
    • 54849183400 scopus 로고    scopus 로고
    • Formal total synthesis of Neopeltolide
    • Vintonyak, V. V., Maier, M. E. (2008). Formal total synthesis of Neopeltolide . Org. Lett., 10, 1239-1242.
    • (2008) Org. Lett., , vol.10 , pp. 1239-1242
    • Vintonyak, V.V.1    Maier, M.E.2
  • 56
    • 34547929795 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of Phthioceranic acid, a heptamethyl-branched acid from mycobacterium tuberculosis
    • Ter Horst, B., Feringa, B. L., Minnaard, A. J. (2007). Catalytic asymmetric synthesis of Phthioceranic acid, a heptamethyl-branched acid from mycobacterium tuberculosis. Org. Lett., 9, 3013-3015.
    • (2007) Org. Lett., , vol.9 , pp. 3013-3015
    • Ter Horst, B.1    Feringa, B.L.2    Minnaard, A.J.3
  • 57
    • 22244475838 scopus 로고    scopus 로고
    • An iterative catalytic route to enantiopure deoxypropionate subunits: asymmetric conjugate addition of Grignard reagents to a, ß-unsaturated thioesters
    • Des Mazery, R., Pullez, M., Lopez, F., Harutyunyan, S. R., Minnaard, A. J., Feringa, B. L. (2005). An iterative catalytic route to enantiopure deoxypropionate subunits: asymmetric conjugate addition of Grignard reagents to a, ß-unsaturated thioesters. J. Am. Chem. Soc., 127, 9966-9967.
    • (2005) J. Am. Chem. Soc., , vol.127 , pp. 9966-9967
    • Des Mazery, R.1    Pullez, M.2    Lopez, F.3    Harutyunyan, S.R.4    Minnaard, A.J.5    Feringa, B.L.6
  • 59
    • 24044546502 scopus 로고    scopus 로고
    • Highly enantioselective Cu-catalyzed conjugate additions of dialkylzinc reagents to unsaturated furanones and pyranones: preparation of air-stable and catalytically active Cu-peptide complexes
    • Brown, M. K., Degrado, S. J., Hoveyda, A. H. (2005). Highly enantioselective Cu-catalyzed conjugate additions of dialkylzinc reagents to unsaturated furanones and pyranones: preparation of air-stable and catalytically active Cu-peptide complexes. Angew. Chem. Int. Ed., 44, 5306-5310.
    • (2005) Angew. Chem. Int. Ed., , vol.44 , pp. 5306-5310
    • Brown, M.K.1    Degrado, S.J.2    Hoveyda, A.H.3
  • 61
    • 34247201978 scopus 로고    scopus 로고
    • All-carbon quaternary stereogenic centers by enantioselective Cu-catalyzed conjugate additions promoted by a chiral N-heterocyclic carbene
    • Brown, M. K., May, T. L., Baxter, C. A., Hoveyda, A. H. (2007). All-carbon quaternary stereogenic centers by enantioselective Cu-catalyzed conjugate additions promoted by a chiral N-heterocyclic carbene. Angew. Chem. Int. Ed., 46, 1097-1100.
    • (2007) Angew. Chem. Int. Ed., , vol.46 , pp. 1097-1100
    • Brown, M.K.1    May, T.L.2    Baxter, C.A.3    Hoveyda, A.H.4
  • 62
    • 67650502255 scopus 로고    scopus 로고
    • A stereodivergent strategy to both product enantiomers from the same enantiomer of a stereoinducing catalyst: Agelastatin A
    • Trost, B. M., Dong, G. (2009). A stereodivergent strategy to both product enantiomers from the same enantiomer of a stereoinducing catalyst: Agelastatin A. Chem.-Eur. J., 15, 6910-6919.
    • (2009) Chem.-Eur. J., , vol.15 , pp. 6910-6919
    • Trost, B.M.1    Dong, G.2
  • 63
    • 70349673170 scopus 로고    scopus 로고
    • Construction of two vicinal quaternary carbons by asymmetric allylic alkylation: total synthesis of Hyperolactone C and (-)-Biyouyanagin A
    • Du, C., Li, L., Li, Y., Xie, Z. (2009). Construction of two vicinal quaternary carbons by asymmetric allylic alkylation: total synthesis of Hyperolactone C and (-)-Biyouyanagin A. Angew. Chem. Int. Ed., 48, 7853-7856.
    • (2009) Angew. Chem. Int. Ed., , vol.48 , pp. 7853-7856
    • Du, C.1    Li, L.2    Li, Y.3    Xie, Z.4
  • 64
    • 0000931564 scopus 로고
    • New synthetic reactions of allyl alkyl carbonates, allyl Î 2-keto carboxylates, and allyl vinylic carbonates catalyzed by palladium complexes
    • Tsuji, J., Minami, I. (1987). New synthetic reactions of allyl alkyl carbonates, allyl Î 2-keto carboxylates, and allyl vinylic carbonates catalyzed by palladium complexes. Acc. Chem. Res., 20, 140-145.
    • (1987) Acc. Chem. Res., , vol.20 , pp. 140-145
    • Tsuji, J.1    Minami, I.2
  • 65
    • 9344253873 scopus 로고    scopus 로고
    • The enantioselective Tsuji allylation
    • Behenna, D. C., Stoltz, B. M. (2004). The enantioselective Tsuji allylation. J. Am. Chem. Soc., 126, 15044-15045.
    • (2004) J. Am. Chem. Soc., , vol.126 , pp. 15044-15045
    • Behenna, D.C.1    Stoltz, B.M.2
  • 66
    • 33745417849 scopus 로고    scopus 로고
    • The catalytic enantioselective, protecting group-free total synthesis of (+)-Dichroanone
    • McFadden, R. M., 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
  • 67
    • 46349090301 scopus 로고    scopus 로고
    • The total synthesis of (-)-Cyanthiwigin F by means of double catalytic enantioselective alkylation
    • Enquist, J. A., Jr, Stoltz, B. M. (2008). The total synthesis of (-)-Cyanthiwigin F by means of double catalytic enantioselective alkylation. Nature, 453, 1228-1231.
    • (2008) Nature, , vol.453 , pp. 1228-1231
    • Enquist, J.A.1    Jr Stoltz, B.M.2
  • 68
    • 18244395541 scopus 로고    scopus 로고
    • The development of enantioselective rhodium-catalyzed hydroboration of olefi ns
    • Carroll, A., O'Sullivan, T. P., Guiry, P. J. (2005). The development of enantioselective rhodium-catalyzed hydroboration of olefi ns. Adv. Synth. Catal., 347, 609-631.
    • (2005) Adv. Synth. Catal., , vol.347 , pp. 609-631
    • Carroll, A.1    O'Sullivan, T.P.2    Guiry, P.J.3
  • 69
    • 34548524556 scopus 로고    scopus 로고
    • Enantioselective synthesis of a trans-7,8-Dimethoxycalamenene
    • Werle, S., Fey, T., Neudoerfl, J. M., Schmalz, H. (2007). Enantioselective synthesis of a trans-7,8-Dimethoxycalamenene. Org. Lett., 9, 3555-3558.
    • (2007) Org. Lett., , vol.9 , pp. 3555-3558
    • Werle, S.1    Fey, T.2    Neudoerfl, J.M.3    Schmalz, H.4
  • 70
    • 34547193192 scopus 로고    scopus 로고
    • Fully reagent-controlled asymmetric synthesis of (-)-Spongidepsin via the Zr-catalyzed asymmetric carboalumination of alkenes (ZACA reaction)
    • Zhu, G., Negishi, E. (2007). Fully reagent-controlled asymmetric synthesis of (-)-Spongidepsin via the Zr-catalyzed asymmetric carboalumination of alkenes (ZACA reaction). Org. Lett., 9, 2771-2774.
    • (2007) Org. Lett., , vol.9 , pp. 2771-2774
    • Zhu, G.1    Negishi, E.2
  • 71
    • 34547160872 scopus 로고    scopus 로고
    • Zirconium-catalyzed asymmetric carboalumination of alkenes: ZACA-lipase-catalyzed acetylation synergy
    • Huang, Z., Tan, Z., Novak, T., Zhu, G., Negishi, E. (2007). Zirconium-catalyzed asymmetric carboalumination of alkenes: ZACA-lipase-catalyzed acetylation synergy. Adv. Synth. Catal., 349, 539-545.
    • (2007) Adv. Synth. Catal., , vol.349 , pp. 539-545
    • Huang, Z.1    Tan, Z.2    Novak, T.3    Zhu, G.4    Negishi, E.5
  • 72
    • 38749127620 scopus 로고    scopus 로고
    • Highly effi cient asymmetric synthesis of Fluvirucinine A1 via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)-lipase-catalyzed acetylation tandem process
    • Liang, B., Negishi, E. (2008). Highly effi cient asymmetric synthesis of Fluvirucinine A1 via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)-lipase-catalyzed acetylation tandem process. Org. Lett., 10, 193-195.
    • (2008) Org. Lett., , vol.10 , pp. 193-195
    • Liang, B.1    Negishi, E.2
  • 75
    • 0042379984 scopus 로고    scopus 로고
    • The asymmetric intramolecular Heck reaction in natural product total synthesis
    • Dounay, A. B., Overman, L. E. (2003). The asymmetric intramolecular Heck reaction in natural product total synthesis . Chem. Rev., 103, 2945-2963.
    • (2003) Chem. Rev., , vol.103 , pp. 2945-2963
    • Dounay, A.B.1    Overman, L.E.2
  • 76
    • 42149168996 scopus 로고    scopus 로고
    • Total synthesis of the strychnos alkaloid (+)-Minfi ensine: tandem enantioselective intramolecular Heck-iminium ion cyclization
    • Dounay, A. B., Humphreys, P. G., Overman, L. E., Wrobleski, A. D. (2008). Total synthesis of the strychnos alkaloid (+)-Minfi ensine: tandem enantioselective intramolecular Heck-iminium ion cyclization . J. Am. Chem. Soc., 130, 5368-5377.
    • (2008) J. Am. Chem. Soc., , vol.130 , pp. 5368-5377
    • Dounay, A.B.1    Humphreys, P.G.2    Overman, L.E.3    Wrobleski, A.D.4
  • 77
    • 33845216121 scopus 로고    scopus 로고
    • Enantioselective palladium-catalyzed total synthesis of vitamin E by employing a domino Wacker-Heck reaction
    • Tietze, L. F., Stecker, F., Zinngrebe, J., Sommer, K. M. (2006). Enantioselective palladium-catalyzed total synthesis of vitamin E by employing a domino Wacker-Heck reaction. Chem. Eur. J., 12, 8770-8776.
    • (2006) Chem. Eur. J., , vol.12 , pp. 8770-8776
    • Tietze, L.F.1    Stecker, F.2    Zinngrebe, J.3    Sommer, K.M.4
  • 80
    • 0034675619 scopus 로고    scopus 로고
    • Catalytic asymmetric hetero-Diels-Alder reactions of carbonyl compounds and imines
    • Jorgensen, K. A. (2000). Catalytic asymmetric hetero-Diels-Alder reactions of carbonyl compounds and imines. Angew. Chem. Int. Ed., 39, 3558-3588.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 3558-3588
    • Jorgensen, K.A.1
  • 81
    • 61849131140 scopus 로고    scopus 로고
    • Asymmetric hetero-Diels-Alder reactions of carbonyl compounds
    • Pellissier, H. (2009). Asymmetric hetero-Diels-Alder reactions of carbonyl compounds. Tetrahedron, 65, 2839-2877.
    • (2009) Tetrahedron, , vol.65 , pp. 2839-2877
    • Pellissier, H.1
  • 82
    • 0033549737 scopus 로고    scopus 로고
    • Highly enantio-and diastereoselective hetero-Diels-Alder reactions catalyzed by new chiral tridentate chromium(III) catalysts
    • Dossetter, A. G., Jamison, T. F., Jacobsen, E. N. (1999). Highly enantio-and diastereoselective hetero-Diels-Alder reactions catalyzed by new chiral tridentate chromium(III) catalysts. Angew. Chem. Int. Ed., 38, 2398-2400.
    • (1999) Angew. Chem. Int. Ed., , vol.38 , pp. 2398-2400
    • Dossetter, A.G.1    Jamison, T.F.2    Jacobsen, E.N.3
  • 83
    • 0037118895 scopus 로고    scopus 로고
    • Highly enantioselective inverse-electron-demand hetero-Diels-Alder reactions of a, ß-unsaturated aldehydes
    • Gademann, K., Chavez, D. E., Jacobsen, E. N. (2002). Highly enantioselective inverse-electron-demand hetero-Diels-Alder reactions of a, ß-unsaturated aldehydes. Angew. Chem. Int. Ed., 41, 3059-3061.
    • (2002) Angew. Chem. Int. Ed., , vol.41 , pp. 3059-3061
    • Gademann, K.1    Chavez, D.E.2    Jacobsen, E.N.3
  • 84
    • 25144436523 scopus 로고    scopus 로고
    • Highly enantio-and regioselective quinone Diels-Alder reactions catalyzed by a tridentate [(Schiff base) CrIII] complex
    • Jarvo, E. R., Lawrence, B. M., Jacobsen, E. N. (2005). Highly enantio-and regioselective quinone Diels-Alder reactions catalyzed by a tridentate [(Schiff base) CrIII] complex. Angew. Chem. Int. Ed., 44, 6043-6046.
    • (2005) Angew. Chem. Int. Ed., , vol.44 , pp. 6043-6046
    • Jarvo, E.R.1    Lawrence, B.M.2    Jacobsen, E.N.3
  • 85
    • 36549023143 scopus 로고    scopus 로고
    • Total synthesis, confi guration, and biological evaluation of Anguinomycin C
    • Bonazzi, S., Guttinger, S., Zemp, I., Kutay, U., Gademann, K. (2007). Total synthesis, confi guration, and biological evaluation of Anguinomycin C. Angew. Chem. Int. Ed., 46, 8707-8710.
    • (2007) Angew. Chem. Int. Ed., , vol.46 , pp. 8707-8710
    • Bonazzi, S.1    Guttinger, S.2    Zemp, I.3    Kutay, U.4    Gademann, K.5
  • 86
    • 54549119239 scopus 로고    scopus 로고
    • Total synthesis of potent antitumor agent (-)-Lasonolide A: a cycloaddition-based strategy
    • Ghosh, A. K., Gong, G. (2008). Total synthesis of potent antitumor agent (-)-Lasonolide A: a cycloaddition-based strategy. Chem.-As. J., 3, 1811-1823.
    • (2008) Chem.-As. J., , vol.3 , pp. 1811-1823
    • Ghosh, A.K.1    Gong, G.2
  • 87
    • 34247536374 scopus 로고    scopus 로고
    • Enantioselective total synthesis of macrolide antitumor agent (-)-Lasonolide A
    • Ghosh, A. K., Gong, G. (2007). Enantioselective total synthesis of macrolide antitumor agent (-)-Lasonolide A. Org. Lett., 9, 1437-1440.
    • (2007) Org. Lett., , vol.9 , pp. 1437-1440
    • Ghosh, A.K.1    Gong, G.2
  • 88
    • 70349098113 scopus 로고    scopus 로고
    • An asymmetric total synthesis of Brevisamide
    • Ghosh, A. K., Li, J. (2009). An asymmetric total synthesis of Brevisamide. Org. Lett., 11, 4164-4167.
    • (2009) Org. Lett., , vol.11 , pp. 4164-4167
    • Ghosh, A.K.1    Li, J.2
  • 89
    • 54749110587 scopus 로고    scopus 로고
    • Total synthesis of the marine macrolide (+)-Neopeltolide
    • Paterson, I., Miller, N. A. (2008). Total synthesis of the marine macrolide (+)-Neopeltolide. Chem. Commun., 4708-4710.
    • (2008) Chem. Commun., , pp. 4708-4710
    • Paterson, I.1    Miller, N.A.2
  • 90
    • 0037018443 scopus 로고    scopus 로고
    • Broadly effective enantioselective Diels-Alder reactions of 1-amino-substituted-1,3-butadienes
    • Huang, Y., Iwama, T., Rawal, V. H. (2002). Broadly effective enantioselective Diels-Alder reactions of 1-amino-substituted-1,3-butadienes. O rg. Lett., 4, 1163-1166.
    • (2002) O rg. Lett., , vol.4 , pp. 1163-1166
    • Huang, Y.1    Iwama, T.2    Rawal, V.H.3
  • 91
    • 0037140734 scopus 로고    scopus 로고
    • Design and development of highly effective Lewis acid catalysts for enantioselective Diels-Alder reactions
    • Huang, Y., Iwama, T., Rawal, V. H. (2002). Design and development of highly effective Lewis acid catalysts for enantioselective Diels-Alder reactions. J. Am. Chem. Soc., 124, 5950-5951.
    • (2002) J. Am. Chem. Soc., , vol.124 , pp. 5950-5951
    • Huang, Y.1    Iwama, T.2    Rawal, V.H.3
  • 94
    • 70350666476 scopus 로고    scopus 로고
    • Total syntheses of (±)-Platencin and (-)-Platencin
    • Nicolaou, K. C., Tria, G. S., Edmonds, D. J., Kar, M. (2009). Total syntheses of (±)-Platencin and (-)-Platencin. J. Am. Chem. Soc., 131, 15909-15917.
    • (2009) J. Am. Chem. Soc., , vol.131 , pp. 15909-15917
    • Nicolaou, K.C.1    Tria, G.S.2    Edmonds, D.J.3    Kar, M.4
  • 95
    • 0028886765 scopus 로고
    • Catalytic enantioselective synthesis of dihydropyrones via formal hetero Diels-Alder reactions of " Danishefsky's diene " with aldehydes
    • Keck, G. E., Li, X., Krishnamurthy, D. (1995). Catalytic enantioselective synthesis of dihydropyrones via formal hetero Diels-Alder reactions of " Danishefsky's diene " with aldehydes. J. Org. Chem., 60, 5998-5999.
    • (1995) J. Org. Chem., , vol.60 , pp. 5998-5999
    • Keck, G.E.1    Li, X.2    Krishnamurthy, D.3
  • 96
    • 70350738387 scopus 로고    scopus 로고
    • A fl exible enantioselective total synthesis of Diospongins A and B and their enantiomers using catalytic hetero-Diels-Alder/Rh-catalyzed 1,4-addition and asymmetric transfer hydrogenation reactions as key steps
    • Kumaraswamy, G., Ramakrishna, G., Naresh, P., Jagadeesh, B., Sridhar, B. (2009). A fl exible enantioselective total synthesis of Diospongins A and B and their enantiomers using catalytic hetero-Diels-Alder/Rh-catalyzed 1,4-addition and asymmetric transfer hydrogenation reactions as key steps. J. Org. Chem., 74, 8468-8471.
    • (2009) J. Org. Chem., , vol.74 , pp. 8468-8471
    • Kumaraswamy, G.1    Ramakrishna, G.2    Naresh, P.3    Jagadeesh, B.4    Sridhar, B.5
  • 97
    • 0000210159 scopus 로고
    • Asymmetric catalysis of Diels-Alder cycloadditions by an MS-free binaphthol-titanium complex: dramatic effect of MS, linear versus positive nonlinear relationship, and synthetic applications
    • Mikami, K., Motoyama, Y., Terada, M. (1994). Asymmetric catalysis of Diels-Alder cycloadditions by an MS-free binaphthol-titanium complex: dramatic effect of MS, linear versus positive nonlinear relationship, and synthetic applications. J. Am. Chem. Soc., 116, 2812-2820.
    • (1994) J. Am. Chem. Soc., , vol.116 , pp. 2812-2820
    • Mikami, K.1    Motoyama, Y.2    Terada, M.3
  • 98
    • 34547207608 scopus 로고    scopus 로고
    • Enantioselective total synthesis of Cyathin A3
    • Ward, D. E., Shen, J. (2007). Enantioselective total synthesis of Cyathin A3. Org. Lett., 9, 2843-2846.
    • (2007) Org. Lett., , vol.9 , pp. 2843-2846
    • Ward, D.E.1    Shen, J.2
  • 99
    • 40949134644 scopus 로고    scopus 로고
    • A direct route to Fluostatin C by a fascinating Diels-Alder reaction
    • Yu, M., Danishefsky, S. J. (2008). A direct route to Fluostatin C by a fascinating Diels-Alder reaction. J. Am. Chem. Soc., 130, 2783-2785.
    • (2008) J. Am. Chem. Soc., , vol.130 , pp. 2783-2785
    • Yu, M.1    Danishefsky, S.J.2
  • 101
    • 34548348368 scopus 로고    scopus 로고
    • Divergent reactions for racemates: catalytic, enantioselective, and regio-divergent nitroso Diels-Alder reactions
    • Jana, C. K., Studer, A. (2007). Divergent reactions for racemates: catalytic, enantioselective, and regio-divergent nitroso Diels-Alder reactions. Angew. Chem. Int. Ed., 46, 6542-6544.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 6542-6544
    • Jana, C.K.1    Studer, A.2
  • 102
    • 53849102181 scopus 로고    scopus 로고
    • Total synthesis of (+)-trans-Dihydronarciclasine by a catalytic enantioselective regiodivergent nitroso Diels-Alder reaction
    • Jana, C. K., Studer, A. (2008). Total synthesis of (+)-trans-Dihydronarciclasine by a catalytic enantioselective regiodivergent nitroso Diels-Alder reaction. Chem.-Eur. J., 14, 6326-6328.
    • (2008) Chem.-Eur. J , vol.14 , pp. 6326-6328
    • Jana, C.K.1    Studer, A.2
  • 103
    • 0036263839 scopus 로고    scopus 로고
    • Catalytic enantioselective Diels-Alder reactions: methods, mechanistic fundamentals, pathways, and applications
    • Corey, E. J. (2002). Catalytic enantioselective Diels-Alder reactions: methods, mechanistic fundamentals, pathways, and applications. Angew. Chem. Int. Ed., 41, 1650-1667.
    • (2002) Angew. Chem. Int. Ed., , vol.41 , pp. 1650-1667
    • Corey, E.J.1
  • 104
    • 0038514123 scopus 로고    scopus 로고
    • Trifl imide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition
    • Ryu, D. H., Corey, E. J. (2003). Trifl imide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition. J. Am. Chem. Soc., 125, 6388-6390.
    • (2003) J. Am. Chem. Soc., , vol.125 , pp. 6388-6390
    • Ryu, D.H.1    Corey, E.J.2
  • 105
    • 31444431583 scopus 로고    scopus 로고
    • Concise total syntheses of Palominol, Dolabellatrienone, ß-Araneosene, and Isoedunol via an enantioselective Diels-Alder macrobicyclization
    • Snyder, S. A., Corey, E. J. (2006). Concise total syntheses of Palominol, Dolabellatrienone, ß-Araneosene, and Isoedunol via an enantioselective Diels-Alder macrobicyclization. J. Am. Chem. Soc., 128, 740-742.
    • (2006) J. Am. Chem. Soc., , vol.128 , pp. 740-742
    • Snyder, S.A.1    Corey, E.J.2
  • 107
    • 84985535088 scopus 로고
    • Chiral copper semicorrin complexes as enantioselective catalysts for the cyclopropanation of olefi ns with diazo compounds
    • Fritschi, H., Leutenegger, U., Pfaltz, A. (1986). Chiral copper semicorrin complexes as enantioselective catalysts for the cyclopropanation of olefi ns with diazo compounds. Angew. Chem. Int. Ed., 25, 1005.
    • (1986) Angew. Chem. Int. Ed , vol.25 , pp. 1005
    • Fritschi, H.1    Leutenegger, U.2    Pfaltz, A.3
  • 110
    • 33846611583 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (+)-Digitoxigenin
    • Honma, M., Nakada, M. (2007). Enantioselective total synthesis of (+)-Digitoxigenin. Tetrahedron Lett., 48, 1541-1544.
    • (2007) Tetrahedron Lett., , vol.48 , pp. 1541-1544
    • Honma, M.1    Nakada, M.2
  • 112
    • 0032567221 scopus 로고    scopus 로고
    • Enantioselective cyclopropanation of allylic alcohols with dioxaborolane ligands: scope and synthetic applications
    • Charette, A. B., Juteau, H., Lebel, H., Molinaro, C. (1998). Enantioselective cyclopropanation of allylic alcohols with dioxaborolane ligands: scope and synthetic applications . J. Am. Chem. Soc., 120, 11943-11952.
    • (1998) J. Am. Chem. Soc., , vol.120 , pp. 11943-11952
    • Charette, A.B.1    Juteau, H.2    Lebel, H.3    Molinaro, C.4
  • 114
    • 0037011303 scopus 로고    scopus 로고
    • [(Arene)Rh(COD)] + complexes as catalysts for [5 + 2] cycloaddition reactions
    • Wender, P. A., Williams, T. J. (2002). [(Arene)Rh(COD)] + complexes as catalysts for [5 + 2] cycloaddition reactions . Angew. Chem. Int. Ed., 41, 4550-4553.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 4550-4553
    • Wender, P.A.1    Williams, T.J.2
  • 115
    • 17444380855 scopus 로고    scopus 로고
    • Syntheses of seven-membered rings: ruthenium-catalyzed intramolecular [5 + 2] cycloadditions
    • Trost, B. M., Shen, H. C., Horne, D. B., Toste, F. D., Steinmetz, B. G., Koradin, C. (2005). Syntheses of seven-membered rings: ruthenium-catalyzed intramolecular [5 + 2] cycloadditions . Chem.-Eur. J., 11, 2577-2590.
    • (2005) Chem.-Eur. J., , vol.11 , pp. 2577-2590
    • Trost, B.M.1    Shen, H.C.2    Horne, D.B.3    Toste, F.D.4    Steinmetz, B.G.5    Koradin, C.6
  • 117
    • 58149163037 scopus 로고    scopus 로고
    • Enantioselective syntheses of carbanucleosides from the Pauson-Khand adduct of trimethylsilylacetylene and norbornadiene
    • Vazquez-Romero, A., Rodriguez, J., Lledo, A., Verdaguer, X., Riera, A. (2008). Enantioselective syntheses of carbanucleosides from the Pauson-Khand adduct of trimethylsilylacetylene and norbornadiene. Org. Lett., 10, 4509-4512.
    • (2008) Org. Lett., , vol.10 , pp. 4509-4512
    • Vazquez-Romero, A.1    Rodriguez, J.2    Lledo, A.3    Verdaguer, X.4    Riera, A.5
  • 118
    • 34447305203 scopus 로고    scopus 로고
    • N-phosphino sulfi namide ligands: an effi cient manner to combine sulfur chirality and phosphorus coordination behavior
    • Solà, J., Revés, M., Riera, A., Verdaguer, X. (2007). N-phosphino sulfi namide ligands: an effi cient manner to combine sulfur chirality and phosphorus coordination behavior. Angew. Chem. Int. Ed., 46, 5020-5023.
    • (2007) Angew. Chem. Int. Ed., , vol.46 , pp. 5020-5023
    • Solà, J.1    Revés, M.2    Riera, A.3    Verdaguer, X.4
  • 119
    • 46649098072 scopus 로고    scopus 로고
    • Cycloisomerization of 1,n-enynes: challenging metal-catalyzed rearrangements and mechanistic insights
    • Michelet, V., Toullec, P. Y., Genet, J. (2008). Cycloisomerization of 1,n-enynes: challenging metal-catalyzed rearrangements and mechanistic insights . Angew. Chem., Inter. Ed., 47, 4268-4315.
    • (2008) Angew. Chem., Inter. Ed , vol.47 , pp. 4268-4315
    • Michelet, V.1    Toullec, P.Y.2    Genet, J.3
  • 120
    • 0026418434 scopus 로고
    • The atom economy: a search for synthetic effi ciency
    • Trost, B. M. (1991). The atom economy: a search for synthetic effi ciency. Science, 254, 1471-1477.
    • (1991) Science, , vol.254 , pp. 1471-1477
    • Trost, B.M.1
  • 121
    • 70450188974 scopus 로고    scopus 로고
    • Total synthesis of Platensimycin and related natural products
    • Nicolaou, K. C., Li, A., Edmonds, D. J., Tria, G. S., Ellery, S. P. (2009). Total synthesis of Platensimycin and related natural products. J. Am. Chem. Soc., 131, 16905-16918
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 16905-16918
    • Nicolaou, K.C.1    Li, A.2    Edmonds, D.J.3    Tria, G.S.4    Ellery, S.P.5
  • 122
    • 0034641228 scopus 로고    scopus 로고
    • Rh-catalyzed enyne cycloisomerization
    • Cao, P., Wang, B., Zhang, X. (2000). Rh-catalyzed enyne cycloisomerization . J. Am. Chem. Soc., 122, 6490-6491.
    • (2000) J. Am. Chem. Soc., , vol.122 , pp. 6490-6491
    • Cao, P.1    Wang, B.2    Zhang, X.3
  • 124
    • 33947273987 scopus 로고    scopus 로고
    • Palladium-catalyzed enantioselective cyclization of silyloxy-1,6-enynes
    • Corkey, B. K., Toste, F. D. (2007). Palladium-catalyzed enantioselective cyclization of silyloxy-1,6-enynes. J. Am. Chem. Soc., 129, 2764-2765.
    • (2007) J. Am. Chem. Soc., , vol.129 , pp. 2764-2765
    • Corkey, B.K.1    Toste, F.D.2
  • 125
    • 0000822354 scopus 로고
    • Stereoselective, one-step assembly of the strained protoilludane framework by cobalt-mediated cyclization of an acyclic enediyne precursor
    • Johnson, E. P., Vollhardt, K. P. C. (1991). Stereoselective, one-step assembly of the strained protoilludane framework by cobalt-mediated cyclization of an acyclic enediyne precursor. A total synthesis of Illudol. J. Am. Chem. Soc., 113, 381-382.
    • (1991) A total synthesis of Illudol. J. Am. Chem. Soc., , vol.113 , pp. 381-382
    • Johnson, E.P.1    Vollhardt, K.P.C.2
  • 126
    • 53749100570 scopus 로고    scopus 로고
    • Novel protoilludane lead structure for veterinary antibiotics: total synthesis of Pasteurestins A and B and assignment of their confi gurations
    • Koegl, M., Brecker, L., Warrass, R., Mulzer, J. (2008). Novel protoilludane lead structure for veterinary antibiotics: total synthesis of Pasteurestins A and B and assignment of their confi gurations . Eur. J. Org. Chem., 2714-2730.
    • (2008) Eur. J. Org. Chem., , pp. 2714-2730
    • Koegl, M.1    Brecker, L.2    Warrass, R.3    Mulzer, J.4
  • 127
    • 71549167603 scopus 로고    scopus 로고
    • Silver and gold catalysis for cycloisomerization reactions
    • Belmont, P., Parker, E. (2009). Silver and gold catalysis for cycloisomerization reactions . Eur. J. Org. Chem., 6075-6089.
    • (2009) Eur. J. Org. Chem., , pp. 6075-6089
    • Belmont, P.1    Parker, E.2
  • 128
    • 68949170987 scopus 로고    scopus 로고
    • Mechanistic insights on the cycloisomerization of polyunsaturated precursors catalyzed by platinum and gold complexes
    • Soriano, E., Marco-Contelles, J. (2009). Mechanistic insights on the cycloisomerization of polyunsaturated precursors catalyzed by platinum and gold complexes . Acc. Chem. Res., 42, 1026-1036.
    • (2009) Acc. Chem. Res., , vol.42 , pp. 1026-1036
    • Soriano, E.1    Marco-Contelles, J.2
  • 129
    • 58949093398 scopus 로고    scopus 로고
    • Recent developments in gold catalysis
    • Gagosz, F. (2009). Recent developments in gold catalysis. Tetrahedron., 65, 1757.
    • (2009) Tetrahedron , vol.65 , pp. 1757
    • Gagosz, F.1
  • 130
    • 77952397509 scopus 로고    scopus 로고
    • Enantioselective synthesis of (-)-Englerins A and B
    • Molawi, K., Delpont, N., Echavarren, A. M. (2010). Enantioselective synthesis of (-)-Englerins A and B. Angew. Chem. Int. Ed., 49, 3517-3519.
    • (2010) Angew. Chem. Int. Ed., , vol.49 , pp. 3517-3519
    • Molawi, K.1    Delpont, N.2    Echavarren, A.M.3
  • 131
    • 77952328004 scopus 로고    scopus 로고
    • Asymmetric, protecting-group-free total synthesis of (-)-Englerin A
    • Zhou, Q., Chen, X., Ma, D. (2010). Asymmetric, protecting-group-free total synthesis of (-)-Englerin A. Angew. Chem. Int. Ed., 49, 3513-3516.
    • (2010) Angew. Chem. Int. Ed., , vol.49 , pp. 3513-3516
    • Zhou, Q.1    Chen, X.2    Ma, D.3
  • 134
    • 34250705242 scopus 로고    scopus 로고
    • Chiral N-heterocyclic carbenes in natural product synthesis: application of Ru-catalyzed asymmetric ring-opening/cross-metathesis and Cu-catalyzed allylic alkylation to total synthesis of Baconipyrone C
    • Gillingham, D. G., Hoveyda, A. H. (2007). Chiral N-heterocyclic carbenes in natural product synthesis: application of Ru-catalyzed asymmetric ring-opening/cross-metathesis and Cu-catalyzed allylic alkylation to total synthesis of Baconipyrone C . Angew. Chem. Int. Ed., 46, 3860-3864.
    • (2007) Angew. Chem. Int. Ed., , vol.46 , pp. 3860-3864
    • Gillingham, D.G.1    Hoveyda, A.H.2
  • 135
    • 20444452821 scopus 로고    scopus 로고
    • Enantioselective synthesis of cyclic amides and amines through Mo-catalyzed asymmetric ring-closing metathesis
    • Sattely, E. S., Cortez, G. A., Moebius, D. C., Schrock, R. R., Hoveyda, A. H. (2005). Enantioselective synthesis of cyclic amides and amines through Mo-catalyzed asymmetric ring-closing metathesis . J. Am. Chem. Soc., 127, 8526-8533.
    • (2005) J. Am. Chem. Soc., , vol.127 , pp. 8526-8533
    • Sattely, E.S.1    Cortez, G.A.2    Moebius, D.C.3    Schrock, R.R.4    Hoveyda, A.H.5
  • 136
    • 61749084132 scopus 로고    scopus 로고
    • Design and stereoselective preparation of a new class of chiral olefi n metathesis catalysts and application to enantioselective synthesis of Quebrachamine: catalyst development inspired by natural product synthesis
    • Sattely, E. S., Meek, S. J., Malcolmson, S. J., Schrock, R. R., Hoveyda, A. H. (2009). Design and stereoselective preparation of a new class of chiral olefi n metathesis catalysts and application to enantioselective synthesis of Quebrachamine: catalyst development inspired by natural product synthesis . J. Am. Chem. Soc., 131, 943-953.
    • (2009) J. Am. Chem. Soc., , vol.131 , pp. 943-953
    • Sattely, E.S.1    Meek, S.J.2    Malcolmson, S.J.3    Schrock, R.R.4    Hoveyda, A.H.5
  • 137
    • 70450204734 scopus 로고    scopus 로고
    • The signifi cance of degenerate processes to enantioselective olefi n metathesis reactions promoted by stereogenic-at-Mo complexes
    • Meek, S. J., Malcolmson, S. J., Li, B., Schrock, R. R., Hoveyda, A. H. (2009). The signifi cance of degenerate processes to enantioselective olefi n metathesis reactions promoted by stereogenic-at-Mo complexes. J. Am. Chem. Soc., 131, 16407-16409.
    • (2009) J. Am. Chem. Soc., , vol.131 , pp. 16407-16409
    • Meek, S.J.1    Malcolmson, S.J.2    Li, B.3    Schrock, R.R.4    Hoveyda, A.H.5
  • 138
    • 20444452821 scopus 로고    scopus 로고
    • Enantioselective synthesis of cyclic amides and amines through Mo-catalyzed asymmetric ring-closing metathesis
    • Sattely, E. S., Cortez, G. A., Moebius, D. C., Schrock, R. R., Hoveyda, A. H. (2005). Enantioselective synthesis of cyclic amides and amines through Mo-catalyzed asymmetric ring-closing metathesis . J. Am. Chem. Soc., 127, 8526-8533.
    • (2005) J. Am. Chem. Soc., , vol.127 , pp. 8526-8533
    • Sattely, E.S.1    Cortez, G.A.2    Moebius, D.C.3    Schrock, R.R.4    Hoveyda, A.H.5
  • 139
    • 0035807528 scopus 로고    scopus 로고
    • Enantioselective ruthenium-catalyzed ring-closing metathesis
    • Seiders, T. J., Ward, D. W., Grubbs, R. H. (2001). Enantioselective ruthenium-catalyzed ring-closing metathesis . Org. Lett., 3, 3225-3228.
    • (2001) Org. Lett., , vol.3 , pp. 3225-3228
    • Seiders, T.J.1    Ward, D.W.2    Grubbs, R.H.3
  • 140
    • 0141885397 scopus 로고    scopus 로고
    • Chiral Ru-based complexes for asymmetric olefi n metathesis: enhancement of catalyst activity through steric and electronic modifi cation
    • Van Veldhuizen, J. J., Gillingham, D. G., Garber, S. B., Kataoka, O., Hoveyda, A. H. (2003). Chiral Ru-based complexes for asymmetric olefi n metathesis: enhancement of catalyst activity through steric and electronic modifi cation . J. Am. Chem. Soc., 125, 12502-12508.
    • (2003) J. Am. Chem. Soc., , vol.125 , pp. 12502-12508
    • Van Veldhuizen, J.J.1    Gillingham, D.G.2    Garber, S.B.3    Kataoka, O.4    Hoveyda, A.H.5
  • 142
    • 70350660793 scopus 로고    scopus 로고
    • Enantioselective synthesis of 5-epi-Citreoviral using ruthenium-catalyzed asymmetric ring-closing metathesis
    • Funk, T. W. (2009). Enantioselective synthesis of 5-epi-Citreoviral using ruthenium-catalyzed asymmetric ring-closing metathesis. O rg. Lett., 11, 4998-5001.
    • (2009) O rg. Lett., , vol.11 , pp. 4998-5001
    • Funk, T.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.