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Volumn 55, Issue 6, 2012, Pages 1097-1100

A new approach to the bicyclo[3.3.1]nonane framework of huperzine A-like molecules via palladium-catalyzed intramolecular γ-arylation

Author keywords

arylation; bicyclo 3.3.1 nonane; huperzine A

Indexed keywords

ARYLATIONS; BICYCLO[3.3.1]NONANE; DIANIONS; DIASTEREOSELECTIVE; HECK REACTIONS; HUPERZINE A; PALLADIUM-CATALYZED; SYNTHETIC STUDY;

EID: 84862568503     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-011-4480-y     Document Type: Conference Paper
Times cited : (4)

References (40)
  • 1
    • 84922342912 scopus 로고
    • The structures of huperzine A and B, two new alkaloids exhibiting marked anticholinesterase activity
    • 10.1139/v86-137 1:CAS:528:DyaL28XkslGqsrY%3D
    • J.-S. Liu Y.-L. Zhu C.-M. Yu Y.-Z. Zhou Y.-Y. Han F.-W. Wu B.-F. Qi 1986 The structures of huperzine A and B, two new alkaloids exhibiting marked anticholinesterase activity Can J Chem 64 837 839 10.1139/v86-137 1:CAS:528:DyaL28XkslGqsrY%3D
    • (1986) Can J Chem , vol.64 , pp. 837-839
    • Liu, J.-S.1    Zhu, Y.-L.2    Yu, C.-M.3    Zhou, Y.-Z.4    Han, Y.-Y.5    Wu, F.-W.6    Qi, B.-F.7
  • 2
    • 0024845473 scopus 로고
    • Alkaloids of Lycopodium selago. On the identity of selagine with huperzine A and the structure of a related alkaloid
    • W.A. Ayer L.M. Browne H. Orszanska Z. Valenta J.-S. Liu 1989 Alkaloids of Lycopodium selago. On the identity of selagine with huperzine A and the structure of a related alkaloid Can J Chem 67 1538 1540 10.1139/v89-234 1:CAS:528:DyaK3cXpsFCmsQ%3D%3D (Pubitemid 20047181)
    • (1989) Canadian Journal of Chemistry , vol.67 , Issue.10 , pp. 1538-1540
    • Ayer, W.A.1    Browne, L.M.2    Orszanska, H.3    Valenta, Z.4    Liu, J.-S.5
  • 3
    • 0345034775 scopus 로고    scopus 로고
    • Chemistry, pharmacology, and clinical efficacy of the Chinese nootropic agent Huperzine A
    • 10.1021/ar9800892 1:CAS:528:DyaK1MXislCnsro%3D
    • A.P. Kozikowski W. Tückmantel 1999 Chemistry, pharmacology, and clinical efficacy of the Chinese nootropic agent Huperzine A Acc Chem Res 32 641 650 10.1021/ar9800892 1:CAS:528:DyaK1MXislCnsro%3D
    • (1999) Acc Chem Res , vol.32 , pp. 641-650
    • Kozikowski, A.P.1    Tückmantel, W.2
  • 4
    • 34247581682 scopus 로고    scopus 로고
    • Development of huperzine A and B for treatment of Alzheimer's disease
    • 10.1351/pac200779040469 1:CAS:528:DC%2BD2sXks1Oit7k%3D
    • D. Bai 2007 Development of huperzine A and B for treatment of Alzheimer's disease Pure Appl Chem 79 469 479 10.1351/pac200779040469 1:CAS:528: DC%2BD2sXks1Oit7k%3D
    • (2007) Pure Appl Chem , vol.79 , pp. 469-479
    • Bai, D.1
  • 5
    • 0024518339 scopus 로고
    • A total synthesis of (+-)-huperzine A
    • DOI 10.1016/S0040-4039(01)93719-0
    • L.J.R. Qia 1989 A total synthesis of (±)-huperzine A Tetrahedron Lett 30 2089 2090 10.1016/S0040-4039(01)93719-0 (Pubitemid 19129744)
    • (1989) Tetrahedron Letters , vol.30 , Issue.16 , pp. 2089-2090
    • Qian, L.1    Ji, R.2
  • 6
    • 0024338668 scopus 로고
    • A practical synthesis of the Chinese 'nootropic' agent huperzine A: A possible lead in the treatment of Alzheimer's disease
    • DOI 10.1021/ja00193a062
    • Y. Xia A. P. Kozikowski 1989 A practical synthesis of the Chinese "Nootropic" agent Huperzine A: A possible lead in the treatment of Alzheimer's disease J Am Chem Soc 111 4116 4117 10.1021/ja00193a062 1:CAS:528:DyaL1MXktVOlt7k%3D (Pubitemid 19138766)
    • (1989) Journal of the American Chemical Society , vol.111 , Issue.11 , pp. 4116-4417
    • Xia, Y.1    Kozikowski, A.P.2
  • 7
    • 0025777337 scopus 로고
    • A route to optically pure (-)-Hupuzine A: Molecular modeling and in vitro pharmacology
    • 10.1021/ja00012a056 1:CAS:528:DyaK3MXkvFaltL8%3D
    • F. Yamada A.P. Kozikowski E.R. Reddy Y.-P. Pang J.H. Miller M. McKinney 1991 A route to optically pure (-)-Hupuzine A: molecular modeling and in vitro pharmacology J Am Chem Soc 113 4695 4696 10.1021/ja00012a056 1:CAS:528:DyaK3MXkvFaltL8%3D
    • (1991) J Am Chem Soc , vol.113 , pp. 4695-4696
    • Yamada, F.1    Kozikowski, A.P.2    Reddy, E.R.3    Pang, Y.-P.4    Miller, J.H.5    McKinney, M.6
  • 9
    • 0002004240 scopus 로고    scopus 로고
    • An enantioselective synthesis of natural (-)-huperzine a via cinchona alkaloids-promoted asymmetric michael reaction
    • S. Kaneko T. Yoshino T. Katoh S. Terashima 1997 An enantioselective synthesis of natural (-)-Huperzine A via cinchona alkaloids-promoted asymmetric Michael reaction Heterocycles 46 27 30 10.3987/COM-96-S4 1:CAS:528: DyaK1cXhvFSktr4%3D (Pubitemid 127740564)
    • (1997) Heterocycles , vol.46 , Issue.1 , pp. 27-30
    • Kaneko, S.1    Yoshino, T.2    Katoh, T.3    Terashima, S.4
  • 10
    • 0030989410 scopus 로고    scopus 로고
    • A novel enantioselective synthesis of the key intermediate of (-)-huperzine A employing asymmetric palladium-catalyzed bicycloannulation
    • DOI 10.1016/S0957-4166(97)00048-7, PII S0957416697000487
    • S. Kaneko T. Yoshino T. Katoh S. Terashima 1997 A novel enantioselective synthesis of the key intermediate of (-)-huperzine A employing asymmetric palladium-catalyzed bicycloannulation Tetrahedron Asymm 8 829 832 10.1016/S0957-4166(97)00048-7 1:CAS:528:DyaK2sXisVWht7w%3D (Pubitemid 27136352)
    • (1997) Tetrahedron Asymmetry , vol.8 , Issue.6 , pp. 829-832
    • Kaneko, S.1    Yoshino, T.2    Katoh, T.3    Terashima, S.4
  • 11
    • 0032554796 scopus 로고    scopus 로고
    • Synthetic studies of huperzine A and its fluorinated analogues. 1. Novel asymmetric syntheses of an enantiomeric pair of huperzine A
    • DOI 10.1016/S0040-4020(98)00227-0, PII S0040402098002270
    • S. Kaneko T. Yoshino T. Katoh S. Terashima 1998 Synthetic studies of Huperzine A and its fluorinated analogues. 1. Novel asymmetric syntheses of an enantiomeric pair of Huperzine A Tetrahedron 54 5471 5484 10.1016/S0040-4020(98) 00227-0 1:CAS:528:DyaK1cXjtValur8%3D (Pubitemid 28288089)
    • (1998) Tetrahedron , vol.54 , Issue.21 , pp. 5471-5484
    • Kaneko, S.1    Yoshino, T.2    Katoh, T.3    Terashima, S.4
  • 12
    • 0033544754 scopus 로고    scopus 로고
    • Asymmetric palladium annulation: Formal synthesis of (+)-huperzine A
    • 10.1016/S0040-4039(99)01874-2 1:CAS:528:DyaK1MXnslOls78%3D
    • C. Chassaing A. Haudrechy Y. Langlois 1999 Asymmetric palladium annulation: formal synthesis of (+)-huperzine A Tetrahedron Lett 40 8805 8809 10.1016/S0040-4039(99)01874-2 1:CAS:528:DyaK1MXnslOls78%3D
    • (1999) Tetrahedron Lett , vol.40 , pp. 8805-8809
    • Chassaing, C.1    Haudrechy, A.2    Langlois, Y.3
  • 13
    • 0034640368 scopus 로고    scopus 로고
    • A formal synthesis of (+)-Huperzine A
    • DOI 10.1016/S0040-4020(00)00227-1, PII S0040402000002271
    • A. Haudrechy C. Chassaing C. Riche Y. Langlois 2000 A formal synthesis of (+)-Huperzine A Tetrahedron 56 3181 3187 10.1016/S0040-4020(00)00227-1 1:CAS:528:DC%2BD3cXjsF2isL8%3D (Pubitemid 30313625)
    • (2000) Tetrahedron , vol.56 , Issue.20 , pp. 3181-3187
    • Haudrechy, A.1    Chassaing, C.2    Riche, C.3    Langlois, Y.4
  • 14
    • 0035931034 scopus 로고    scopus 로고
    • Studies on the asymmetric synthesis of huperzine A. Part 2: Highly enantioselective palladium-catalyzed bicycloannulation of the β-keto-ester using new chiral ferrocenylphosphine ligands
    • DOI 10.1016/S0957-4166(02)00006-X, PII S095741660200006X
    • X.-C. He B. Wang G. Yu D. Bai 2001 Studies on the asymmetric synthesis of huperzine A. Part 2: Highly enantioselective palldium-catalyzed bicycloannulation of the β-keto-ester using new chiral ferrocenylphosphine ligands Tetrahedron Asymm 12 3213 3216 10.1016/S0957-4166(02)00006-X 1:CAS:528:DC%2BD38XhtFKqsL4%3D (Pubitemid 34159161)
    • (2001) Tetrahedron Asymmetry , vol.12 , Issue.23 , pp. 3213-3216
    • He, X.-C.1    Wang, B.2    Yu, G.3    Bai, D.4
  • 15
    • 0037170640 scopus 로고    scopus 로고
    • Synthesis of huperzine intermediates via Mn(III)-mediated radical cyclization
    • DOI 10.1016/S0040-4039(02)00270-8, PII S0040403902002708
    • I.Y.C. Lee M.H. Jung H.W. Lee J.Y. Yang 2002 Synthesis of huperzine intermediates via Mn(III)-mediated radical cyclization Tetrahedron Lett 43 2407 2409 10.1016/S0040-4039(02)00270-8 1:CAS:528:DC%2BD38XhvFOntbY%3D (Pubitemid 34230465)
    • (2002) Tetrahedron Letters , vol.43 , Issue.13 , pp. 2407-2409
    • Lee, I.Y.C.1    Jung, M.H.2    Lee, H.W.3    Yang, J.Y.4
  • 16
    • 29144461674 scopus 로고    scopus 로고
    • Chiral guanidine catalyzed annulation to the core structure of (-)-Huperzine A
    • 10.1002/cjoc.20030210716 1:CAS:528:DC%2BD3sXls1Wku7Y%3D
    • Q.-B. Pan D.-W. Ma 2003 Chiral guanidine catalyzed annulation to the core structure of (-)-Huperzine A Chin J Chem 21 793 796 10.1002/cjoc.20030210716 1:CAS:528:DC%2BD3sXls1Wku7Y%3D
    • (2003) Chin J Chem , vol.21 , pp. 793-796
    • Pan, Q.-B.1    Ma, D.-W.2
  • 17
    • 29144523556 scopus 로고    scopus 로고
    • A radical mediated approach to the core structure of huperzine A
    • DOI 10.1016/j.tetlet.2005.11.037, PII S0040403905024858
    • J. Ward V. Caprio 2006 A radical mediated approach to the core structure of huperzine A Tetrahedron Lett 47 553 556 10.1016/j.tetlet.2005.11.037 1:CAS:528:DC%2BD2MXhtlantLfL (Pubitemid 41797396)
    • (2006) Tetrahedron Letters , vol.47 , Issue.4 , pp. 553-556
    • Ward, J.1    Caprio, V.2
  • 18
    • 33846046387 scopus 로고    scopus 로고
    • A concise and convergent (formal) total synthesis of huperzine A
    • DOI 10.1039/b615059d
    • C. Lucey S.A. Kelly J. Mann 2007 A concise and convergent (formal) total synthesis of huperzine A Org Biomol Chem 5 301 306 10.1039/b615059d 1:CAS:528:DC%2BD2sXhtlSguw%3D%3D (Pubitemid 46058479)
    • (2007) Organic and Biomolecular Chemistry , vol.5 , Issue.2 , pp. 301-306
    • Lucey, C.1    Kelly, S.A.2    Mann, J.3
  • 19
    • 67749093213 scopus 로고    scopus 로고
    • Synthesis of the bicyclo[3.3.1]nonane core of Huperzine A and novel pyridine-fused tricycles by cyclisation of pyridine-based radicals
    • 10.3987/COM-08-S(D)48 1:CAS:528:DC%2BD1MXltlaisrs%3D
    • J. Ward V. Caprio 2009 Synthesis of the bicyclo[3.3.1]nonane core of Huperzine A and novel pyridine-fused tricycles by cyclisation of pyridine-based radicals Heterocycles 79 791 804 10.3987/COM-08-S(D)48 1:CAS:528: DC%2BD1MXltlaisrs%3D
    • (2009) Heterocycles , vol.79 , pp. 791-804
    • Ward, J.1    Caprio, V.2
  • 20
    • 70749110705 scopus 로고    scopus 로고
    • Total synthesis of (-)-Huperzine A
    • 10.1021/ol9022408 1:CAS:528:DC%2BD1MXhtleisLvK
    • T. Koshiba S. Yokoshima T. Fukuyama 2009 Total synthesis of (-)-Huperzine A Org Lett 11 5354 5356 10.1021/ol9022408 1:CAS:528:DC%2BD1MXhtleisLvK
    • (2009) Org Lett , vol.11 , pp. 5354-5356
    • Koshiba, T.1    Yokoshima, S.2    Fukuyama, T.3
  • 21
    • 79953207640 scopus 로고    scopus 로고
    • Concise approach to the core of englerin A via an organocatalytic [4+3] cycloaddition reaction
    • 10.1016/j.tetlet.2010.11.087 1:CAS:528:DC%2BC3MXkt1yktr8%3D
    • B.-F. Sun C.-L. Wang R. Ding J.-Y. Xu G.-Q. Lin 2011 Concise approach to the core of englerin A via an organocatalytic [4+3] cycloaddition reaction Tetrahedron Lett 52 2155 2158 10.1016/j.tetlet.2010.11.087 1:CAS:528: DC%2BC3MXkt1yktr8%3D
    • (2011) Tetrahedron Lett , vol.52 , pp. 2155-2158
    • Sun, B.-F.1    Wang, C.-L.2    Ding, R.3    Xu, J.-Y.4    Lin, G.-Q.5
  • 22
    • 28844457939 scopus 로고    scopus 로고
    • Stereospecific rearrangement of α-hydroxyepoxide: Efficient approach to the trans-bicyclo[9.3.0]tetradecane core en route to clavulactone
    • DOI 10.1016/j.tetlet.2005.11.021, PII S0040403905024561
    • B. Sun X. Xu 2006 Stereospecific rearrangement of α-hydroxyepoxide: efficient approach to the trans-bicyclo[9.3.0]tetradecane core en route to clavulactone Tetrahedron Lett 47 299 302 10.1016/j.tetlet.2005.11.021 1:CAS:528:DC%2BD2MXht12qsbrF (Pubitemid 41770818)
    • (2006) Tetrahedron Letters , vol.47 , Issue.3 , pp. 299-302
    • Sun, B.1    Xu, X.2
  • 23
    • 27644505563 scopus 로고    scopus 로고
    • General synthetic approach to bicyclo[9.3.0]tetradecenone: A versatile intermediate to clavulactone and clavirolides
    • DOI 10.1016/j.tetlet.2005.09.106, PII S0040403905020812
    • B. Sun X. Xu 2005 General synthetic approach to bicyclo[9.3.0] tetradecenone: A versatile intermediate to clavulactone and clavirolides Tetrahedron Lett 46 8431 8434 10.1016/j.tetlet.2005.09.106 1:CAS:528: DC%2BD2MXhtFKnsrbF (Pubitemid 41560880)
    • (2005) Tetrahedron Letters , vol.46 , Issue.48 , pp. 8431-8434
    • Sun, B.1    Xu, X.2
  • 25
    • 77954632546 scopus 로고    scopus 로고
    • Total synthesis of (±)-Aplykurodinone-1: Traceless stereochemical guidance
    • 10.1021/ja1035495 1:CAS:528:DC%2BC3cXmslels7o%3D
    • Y. Zhang S.J. Danishefsky 2010 Total synthesis of (±)- Aplykurodinone-1: Traceless stereochemical guidance J Am Chem Soc 132 9567 9569 10.1021/ja1035495 1:CAS:528:DC%2BC3cXmslels7o%3D
    • (2010) J Am Chem Soc , vol.132 , pp. 9567-9569
    • Zhang, Y.1    Danishefsky, S.J.2
  • 26
    • 0026584198 scopus 로고
    • Stereoselective total synthesis of (+)-artemisinin, the antimalarial constituent of Artemisia annua L
    • 10.1021/ja00029a028 1:CAS:528:DyaK38XlvFKmsg%3D%3D
    • M.A. Avery W.K.M. Chong C. Jennings-White 1992 Stereoselective total synthesis of (+)-artemisinin, the antimalarial constituent of Artemisia annua L J Am Chem Soc 114 974 979 10.1021/ja00029a028 1:CAS:528:DyaK38XlvFKmsg%3D%3D
    • (1992) J Am Chem Soc , vol.114 , pp. 974-979
    • Avery, M.A.1    Chong, W.K.M.2    Jennings-White, C.3
  • 27
    • 0000365487 scopus 로고    scopus 로고
    • Novel and selective α-substitution of ketones and other carbonyl compounds based on Pd-catalyzed cross coupling of α,β-unsaturated carbonyl derivatives containing α-halogen or α-metal groups
    • PII S0022328X98010572
    • E. Negishi 1999 Novel and selective α-substitution of ketones and other carbonyl compounds based on Pd-catalyzed cross coupling of α,β-unsaturated carbonyl derivatives containing a-halogen or α-metal groups J Organomet Chem 576 179 194 10.1016/S0022-328X(98)01057-2 1:CAS:528:DyaK1MXivFOlsrs%3D (Pubitemid 129595975)
    • (1999) Journal of Organometallic Chemistry , vol.576 , Issue.1-2 , pp. 179-194
    • Negishi, E.-I.1
  • 28
    • 33748621833 scopus 로고
    • A simple catalytic method for the conversion of aryl bromides to arylamines
    • 10.1002/anie.199513481 1:CAS:528:DyaK2MXmvV2msr8%3D
    • A. S. Guram R.A. Rennels S.L. Buchwald 1995 A simple catalytic method for the conversion of aryl bromides to arylamines Angew Chem, Int Engl 34 1348 1350 10.1002/anie.199513481 1:CAS:528:DyaK2MXmvV2msr8%3D
    • (1995) Angew Chem, Int Engl , vol.34 , pp. 1348-1350
    • Guram, A.S.1    Rennels, R.A.2    Buchwald, S.L.3
  • 29
    • 0029044538 scopus 로고
    • Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents
    • 10.1016/0040-4039(95)00605-C 1:CAS:528:DyaK2MXmtFCjtLo%3D
    • J. Louie J.F. Hartwig 1995 Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents Tetrahedron Lett 36 3609 3612 10.1016/0040-4039(95)00605-C 1:CAS:528:DyaK2MXmtFCjtLo%3D
    • (1995) Tetrahedron Lett , vol.36 , pp. 3609-3612
    • Louie, J.1    Hartwig, J.F.2
  • 30
    • 33746658046 scopus 로고    scopus 로고
    • Stereoselective synthesis of pyridinones: Application to the synthesis of (-)-barrenazines
    • DOI 10.1021/ol0609006
    • T. Focken A.B. Charette 2006 Stereoselective synthesis of pyridinones: application to the synthesis of (-)-Barrenazines Org Lett 8 2985 2988 10.1021/ol0609006 1:CAS:528:DC%2BD28XlvFentbY%3D (Pubitemid 44154411)
    • (2006) Organic Letters , vol.8 , Issue.14 , pp. 2985-2988
    • Focken, T.1    Charette, A.B.2
  • 31
    • 0001236804 scopus 로고    scopus 로고
    • Synthesis of 2-anilinotropones via palladium-catalyzed amination of 2-triflatotropone
    • 10.1021/ol991310t 1:CAS:528:DyaK1MXotVOmtLw%3D
    • F.A. Hicks M. Brookhart 2000 Synthesis of 2-anilinotropones via palladium-catalyzed amination of 2-triflatotropone Org Lett 2 219 221 10.1021/ol991310t 1:CAS:528:DyaK1MXotVOmtLw%3D
    • (2000) Org Lett , vol.2 , pp. 219-221
    • Hicks, F.A.1    Brookhart, M.2
  • 32
    • 69149099056 scopus 로고    scopus 로고
    • A convenient synthesis of 5-arylamino-4H-pyran-4-ones using palladium-catalyzed amination
    • 10.1016/j.tetlet.2009.07.139 1:CAS:528:DC%2BD1MXhtVeqtrrI
    • J. Farard C. Logé B. Pfeiffer B. Lesur M. Duflos 2009 A convenient synthesis of 5-arylamino-4H-pyran-4-ones using palladium-catalyzed amination Tetrahedron Lett 50 5729 5732 10.1016/j.tetlet.2009.07.139 1:CAS:528: DC%2BD1MXhtVeqtrrI
    • (2009) Tetrahedron Lett , vol.50 , pp. 5729-5732
    • Farard, J.1    Logé, C.2    Pfeiffer, B.3    Lesur, B.4    Duflos, M.5
  • 33
    • 0041317683 scopus 로고    scopus 로고
    • A convergent approach to huperzine A and analogues
    • 10.1039/b305869g 1:CAS:528:DC%2BD3sXmtVGqur8%3D
    • S.A. Kelly Y. Foricher J. Mann J.M. Bentley 2003 A convergent approach to huperzine A and analogues Org Biomol Chem 1 2865 2876 10.1039/b305869g 1:CAS:528:DC%2BD3sXmtVGqur8%3D
    • (2003) Org Biomol Chem , vol.1 , pp. 2865-2876
    • Kelly, S.A.1    Foricher, Y.2    Mann, J.3    Bentley, J.M.4
  • 34
    • 0000586350 scopus 로고
    • α,N-alkanesulfonamide dianions: Formation and chemoselective C-alkylation
    • 10.1021/jo00184a006 1:CAS:528:DyaL2cXhvFWgsLw%3D
    • M.E. Thompson 1984 α,N-alkanesulfonamide dianions: formation and chemoselective C-alkylation J Org Chem 49 1700 1703 10.1021/jo00184a006 1:CAS:528:DyaL2cXhvFWgsLw%3D
    • (1984) J Org Chem , vol.49 , pp. 1700-1703
    • Thompson, M.E.1
  • 35
    • 0000276081 scopus 로고
    • Metalation at methyl group of N-substituted o-toluenesulfonamides by excess n-butyllithium. condensation with benzophenone
    • 10.1021/jo01275a063 1:CAS:528:DyaF1MXhtFantg%3D%3D
    • H. Watanabe C.R. Hauser 1968 Metalation at methyl group of N-substituted o-toluenesulfonamides by excess n-butyllithium. condensation with benzophenone J Org Chem 33 4278 4279 10.1021/jo01275a063 1:CAS:528:DyaF1MXhtFantg%3D%3D
    • (1968) J Org Chem , vol.33 , pp. 4278-4279
    • Watanabe, H.1    Hauser, C.R.2
  • 36
    • 0344082863 scopus 로고    scopus 로고
    • Practical Synthesis of Sultams via Sulfonamide Dianion Alkylation: Application to the Synthesis of Chiral Sultams
    • DOI 10.1021/ol0356183
    • J. Lee Y.-L. Zhong R.A. Reamer D. Askin 2003 Practical synthesis of sultams via sulfonamide dianion alkylation: Application to the synthesis of chiral sultams Org Lett 5 4175 4177 10.1021/ol0356183 1:CAS:528: DC%2BD3sXnvFOisbg%3D (Pubitemid 37449618)
    • (2003) Organic Letters , vol.5 , Issue.22 , pp. 4175-4177
    • Lee, J.1    Zhong, Y.-L.2    Reamer, R.A.3    Askin, D.4
  • 37
    • 0000685585 scopus 로고
    • Mn(III)-based oxidative free radical cyclization of unsaturated ketones
    • 10.1021/jo00122a006 1:CAS:528:DyaK2MXnsVKqsbo%3D
    • B. B. Snider B.M. Cole 1995 Mn(III)-based oxidative free radical cyclization of unsaturated ketones J Org Chem 60 5376 5377 10.1021/jo00122a006 1:CAS:528:DyaK2MXnsVKqsbo%3D
    • (1995) J Org Chem , vol.60 , pp. 5376-5377
    • Snider, B.B.1    Cole, B.M.2
  • 38
    • 79960897911 scopus 로고    scopus 로고
    • Stereoselective synthesis of highly substituted enamides by an oxidative Heck reaction
    • 10.1002/anie.201101550 1:CAS:528:DC%2BC3MXotV2htbc%3D
    • Y. Liu D. Li C.-M. Park 2011 Stereoselective synthesis of highly substituted enamides by an oxidative Heck reaction Angew Chem, Int Ed 50 7333 7336 10.1002/anie.201101550 1:CAS:528:DC%2BC3MXotV2htbc%3D
    • (2011) Angew Chem, Int Ed , vol.50 , pp. 7333-7336
    • Liu, Y.1    Li, D.2    Park, C.-M.3
  • 39
    • 10044267678 scopus 로고    scopus 로고
    • Direct oxidative heck cyclizations: Intramolecular Fujiwara-Moritani arylations for the synthesis of functionalized benzofurans and dihydrobenzofurans
    • DOI 10.1002/anie.200461294
    • H. Zhang E.M. Ferreira B.M. Stoltz 2004 Direct oxidative Heck cyclizations: Intramolecular Fujiwara-Moritani arylations for the synthesis of functionalized benzofurans and dihydrobenzofurans Angew Chem, Int Ed 43 6144 6148 10.1002/anie.200461294 1:CAS:528:DC%2BD2cXhtVKgsrbF (Pubitemid 39611881)
    • (2004) Angewandte Chemie - International Edition , vol.43 , Issue.45 , pp. 6144-6148
    • Zhang, H.1    Ferreira, E.M.2    Stoltz, B.M.3
  • 40
    • 3543120754 scopus 로고    scopus 로고
    • The total synthesis of (+)-dragmacidin F
    • DOI 10.1021/ja046695b
    • N.K. Garg D.D. Caspi B.M. Stoltz 2004 The total synthesis of (+)-dragmacidin F J Am Chem Soc 126 9552 9553 10.1021/ja046695b 1:CAS:528:DC%2BD2cXlvVSksbw%3D (Pubitemid 39031037)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.31 , pp. 9552-9553
    • Garg, N.K.1    Caspi, D.D.2    Stoltz, B.M.3


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