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Volumn 111, Issue 20, 1989, Pages 8036-8037

An Enantioselective and Highly Convergent Synthesis of (+)-Ikarugamycin

Author keywords

[No Author keywords available]

Indexed keywords

IKARUGAMYCIN;

EID: 0024422299     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00202a066     Document Type: Article
Times cited : (95)

References (17)
  • 3
    • 0021075328 scopus 로고
    • For other approaches to the carbocyclic system of 1, see: Whitesell, J. K.; Minton, M. A. J. Am. Chem. Soc. 1987, 109, 6403 and references therein
    • Boeckman, R. K. Jr.; Napier, J. J.; Thomas, E. W.; Sato, R. I. J. Org. Chem. 1983, 48, 4152. For other approaches to the carbocyclic system of 1, see: Whitesell, J. K.; Minton, M. A. J. Am. Chem. Soc. 1987, 109, 6403 and references therein.
    • (1983) J. Org. Chem. , vol.48 , pp. 4152
    • Boeckman, R.K.1    Napier, J.J.2    Thomas, E.W.3    Sato, R.I.4
  • 4
    • 0022899041 scopus 로고
    • For a discussion of the various synthetic strategies for formation of the macrocyclic ring
    • For a discussion of the various synthetic strategies for formation of the macrocyclic ring, see: Boeckman, R. K., Jr.; Perni, R. B. J. Org. Chem. 1986, 51, 5486.
    • (1986) J. Org. Chem. , vol.51 , pp. 5486
    • Boeckman, R.K.1    Perni, R.B.2
  • 5
    • 0024451471 scopus 로고
    • See the following paper in this issue for an alternative total synthesis of (+)-1 by Paquette and co-workers
    • following paper in this issue
    • See the following paper in this issue for an alternative total synthesis of (+)-1 by Paquette and co-workers: Paquette, L. A.; Macdonald, D.; Anderson, L.; Wright, J. J. Am. Chem. Soc. 1989, 111, following paper in this issue.
    • (1989) J. Am. Chem. Soc. , vol.111
    • Paquette, L.A.1    Macdonald, D.2    Anderson, L.3    Wright, J.4
  • 6
    • 0000847570 scopus 로고
    • Use of highly electrophilic oxidants was precluded by the unexpectedly high reactivity of the strained double bond in 2
    • Moriarity, R. M.; Hou, K. C. Tetrahedron Lett. 1984, 25, 691. Use of highly electrophilic oxidants was precluded by the unexpectedly high reactivity of the strained double bond in 2.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 691
    • Moriarity, R.M.1    Hou, K.C.2
  • 8
    • 33847802666 scopus 로고
    • For an example of a similar epimerization
    • For an example of a similar epimerization, see: Corey, E. J.; Wollenberg, R. H. J. Org. Chem. 1975, 40, 2265.
    • (1975) J. Org. Chem. , vol.40 , pp. 2265
    • Corey, E.J.1    Wollenberg, R.H.2
  • 9
    • 0000293918 scopus 로고
    • Boeckman, R. K., Jr.; Perni, R. B.; McDonald, J. E.; Thomas, A. J. Org. Synth. 1987, 66, 194
    • Boeckman, R. K., Jr.; Thomas, A. J. J. Org. Chem. 1982, 47, 2823. Boeckman, R. K., Jr.; Perni, R. B.; McDonald, J. E.; Thomas, A. J. Org. Synth. 1987, 66, 194.
    • (1982) J. Org. Chem. , vol.47 , pp. 2823
    • Boeckman, R.K.1    Thomas, A.J.2
  • 12
    • 0001584239 scopus 로고
    • Tetrahedron Lett
    • Jeffrey, P. D.; McCombie, S. W. J. Org. Chem. 1982, 47, 587
    • Tsuji, J.; Yamakawa, T. Tetrahedron Lett. 1979, 20, 613. Jeffrey, P. D.; McCombie, S. W. J. Org. Chem. 1982, 47, 587.
    • (1979) , vol.20 , pp. 613
    • Tsuji, J.1    Yamakawa, T.2
  • 15
    • 0000728075 scopus 로고
    • Clemens, R. J.; Hyatt, J. A. J. Org. Chem. 1985, 50, 2431
    • Hyatt, J. A.; Feldman, P. L.; Clemens, R. J. J. Org. Chem. 1984, 49, 5105. Clemens, R. J.; Hyatt, J. A. J. Org. Chem. 1985, 50, 2431.
    • (1984) J. Org. Chem. , vol.49 , pp. 5105
    • Hyatt, J.A.1    Feldman, P.L.2    Clemens, R.J.3
  • 16
    • 0003003971 scopus 로고
    • Use of aprotic solvents for formation of 16 and related tetramic acids is distinctly inferior to t-BuOH both in terms of yield and production of pure products
    • Lacey, R. N. J. Chem. Soc. 1954, 850. Use of aprotic solvents for formation of 16 and related tetramic acids is distinctly inferior to t-BuOH both in terms of yield and production of pure products.
    • (1954) J. Chem. Soc. , pp. 850
    • Lacey, R.N.1
  • 17
    • 0021952325 scopus 로고
    • Deshong, P.; Ramesh, S.; Elango, V.; Perez, J. J. J. Am. Chem. Soc. 1985, 107, 5219. Boeckman, R. K., Jr.; Starrett, J. E.: Nickell. D. G.: Sum. P.-E. J. Am. Chem. Soc. 1986. 108. 5549
    • Schlessinger, R. H.; Bebernitz, G. R.; Lin, P.; Poss, A. J. J. Am. Chem. Soc. 1985, 107, 1777. Deshong, P.; Ramesh, S.; Elango, V.; Perez, J. J. J. Am. Chem. Soc. 1985, 107, 5219. Boeckman, R. K., Jr.; Starrett, J. E.: Nickell. D. G.: Sum. P.-E. J. Am. Chem. Soc. 1986. 108. 5549.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 1777
    • Schlessinger, R.H.1    Bebernitz, G.R.2    Lin, P.3    Poss, A.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.