메뉴 건너뛰기




Volumn , Issue 14, 2007, Pages 2147-2157

Asymmetric hetero-Diels-Alder reactions of Danishefsky's and Brassard's dienes with aldehydes

Author keywords

Asymmetric catalysis; Diels Alder reactions; Heterocycles; Lewis acids; Schiff bases

Indexed keywords

2,2' DIHYDROXY 1,1' BINAPHTHYL; ALDEHYDE DERIVATIVE; ALKADIENE; COPPER DERIVATIVE; SCHIFF BASE; TETRAISOPROPOXYTITANIUM; TITANIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34548807523     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-984917     Document Type: Review
Times cited : (81)

References (148)
  • 1
    • 0036263839 scopus 로고    scopus 로고
    • For some reviews on the hetero-Diels-Alder reaction, see: a
    • For some reviews on the hetero-Diels-Alder reaction, see: (a) Corey, E. J. Angew. Chem. Int. Ed. 2002, 41, 1650.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 1650
    • Corey, E.J.1
  • 7
    • 0344835672 scopus 로고    scopus 로고
    • For some recent works on hetero-Diels-Alder reactions, see: a
    • For some recent works on hetero-Diels-Alder reactions, see: (a) Juhl, K.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2003, 42, 1498.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 1498
    • Juhl, K.1    Jørgensen, K.A.2
  • 13
    • 0000016331 scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Danishefsky, S. Acc. Chem. Res. 1981, 14, 400.
    • (1981) Acc. Chem. Res , vol.14 , pp. 400
    • Danishefsky, S.1
  • 16
    • 0000884707 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon: New York
    • (d) Boger, D. L. In Comprehensive Organic Synthesis, Vol. 5; Trost, B. M.; Fleming, I., Eds.; Pergamon: New York, 1991, 451.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 451
    • Boger, D.L.1
  • 40
    • 33751391798 scopus 로고    scopus 로고
    • G ao, Q.; Maruyama, T.; Mouri, M.; Yamamoto, H. J. Org. Chem. 1992, 57, 1951.
    • (a) G ao, Q.; Maruyama, T.; Mouri, M.; Yamamoto, H. J. Org. Chem. 1992, 57, 1951.
  • 70
    • 33745683617 scopus 로고    scopus 로고
    • For a review on recent progress in chiral Brønsted acid catalysis, see: c
    • For a review on recent progress in chiral Brønsted acid catalysis, see: (c) Akiyama, T.; Itoh, J.; Fuchibe, K. Adv. Synth. Catal. 2006, 348, 999.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 999
    • Akiyama, T.1    Itoh, J.2    Fuchibe, K.3
  • 86
    • 0024440093 scopus 로고
    • For a review on 5,6-dihydro-2-pyrones, see: a, Herz, W, Grisebach, H, Kirby, G. W, Tamm, C, Eds, Springer: New York
    • For a review on 5,6-dihydro-2-pyrones, see: (a) Davies-Coleman, M. T.; Rivett, D. E. A. In Progress in the Chemistry of Organic Natural Products, Vol. 55; Herz, W.; Grisebach, H.; Kirby, G. W.; Tamm, C., Eds.; Springer: New York, 1989, 1.
    • (1989) Progress in the Chemistry of Organic Natural Products , vol.55 , pp. 1
    • Davies-Coleman, M.T.1    Rivett, D.E.A.2
  • 92
    • 0141508044 scopus 로고    scopus 로고
    • For some examples by annulation of open-chain precursors, see: a
    • For some examples by annulation of open-chain precursors, see: (a) Mulzer, J.; Öhler, E. Chem. Rev. 2003, 103, 3753.
    • (2003) Chem. Rev , vol.103 , pp. 3753
    • Mulzer, J.1    Öhler, E.2
  • 110
    • 18044399640 scopus 로고    scopus 로고
    • By vinylogous aldol reactions: (a) Bluet, G.; Bazán-Tejeda, B.; Campagne, J.-M. Org. Lett. 2001, 3, 3807.
    • By vinylogous aldol reactions: (a) Bluet, G.; Bazán-Tejeda, B.; Campagne, J.-M. Org. Lett. 2001, 3, 3807.
  • 113
    • 34548800777 scopus 로고    scopus 로고
    • By the oxidation of lactols or hexoses: (a) See also ref. 2d
    • By the oxidation of lactols or hexoses: (a) See also ref. 2d
  • 116
    • 0001693882 scopus 로고    scopus 로고
    • By derivation from dihydropyrones or dihydropyrans: (a) Yamashita, Y.; Saito, S.; Ishitani, H.; Kobayashi, S. Org. Lett. 2002, 4, 1221.
    • By derivation from dihydropyrones or dihydropyrans: (a) Yamashita, Y.; Saito, S.; Ishitani, H.; Kobayashi, S. Org. Lett. 2002, 4, 1221.
  • 118
    • 0034703753 scopus 로고    scopus 로고
    • By the two-step addition reaction of ene to dicarbonyl compounds: Audrain, H.; Jørgensen, K. A. J. Am. Chem. Soc. 2000, 122, 11543.
    • By the two-step addition reaction of ene to dicarbonyl compounds: Audrain, H.; Jørgensen, K. A. J. Am. Chem. Soc. 2000, 122, 11543.
  • 119
    • 0010218582 scopus 로고
    • By hetero-Diels-Alder reactions, see: a
    • By hetero-Diels-Alder reactions, see: (a) Castellino, S.; Sims, J. J. Tetrahedron Lett. 1984, 25, 2307.
    • (1984) Tetrahedron Lett , vol.25 , pp. 2307
    • Castellino, S.1    Sims, J.J.2
  • 121
    • 33750286507 scopus 로고    scopus 로고
    • For some very recent works on δ-lactones, see: a
    • For some very recent works on δ-lactones, see: (a) Dieter, R. K.; Guo, F. Org. Lett. 2006, 8, 4779.
    • (2006) Org. Lett , vol.8 , pp. 4779
    • Dieter, R.K.1    Guo, F.2
  • 138
    • 33750479505 scopus 로고    scopus 로고
    • For some recent works on Brassard's diene, see: a
    • For some recent works on Brassard's diene, see: (a) Yoshino, T.; Ng, F.; Danishefsky, S. J. J. Am. Chem. Soc. 2006, 128, 14185.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 14185
    • Yoshino, T.1    Ng, F.2    Danishefsky, S.J.3
  • 145
    • 0003021424 scopus 로고    scopus 로고
    • Meijere, A, Houk, K. N, Ley, S. V, Thiem, J, Trost, B. M, Vögtle, F, Yamamoto, H, Eds, Springer: Berlin
    • (a) Staunton, J.; Wilkinson, B. In Topics in Current Chemistry, Vol. 195; Meijere, A.; Houk, K. N.; Ley, S. V.; Thiem, J.; Trost, B. M.; Vögtle, F.; Yamamoto, H., Eds.; Springer: Berlin, 1997, 49.
    • (1997) Topics in Current Chemistry , vol.195 , pp. 49
    • Staunton, J.1    Wilkinson, B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.