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Volumn 39, Issue 30, 1998, Pages 5377-5380

A formal synthesis of (+)-brefeldin A

Author keywords

[No Author keywords available]

Indexed keywords

BREFELDIN A; CYCLOPENTANE DERIVATIVE;

EID: 0032560770     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01078-8     Document Type: Article
Times cited : (17)

References (23)
  • 1
    • 0029010279 scopus 로고
    • Other related references are cited therein
    • 1. For the recent synthesis of (+)-brefeldin A, see: Kim, D; Lim, J. I. Tetrahedron Lett. 1995, 36, 5035. Other related references are cited therein.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 5035
    • Kim, D.1    Lim, J.I.2
  • 3
    • 0021720782 scopus 로고
    • 2. a) Kitahara, T.; Mori, K.; Matsui, M. Tetrahedron Lett. 1979, 3021. Kitahara, T.; Mori, K Tetrahedron, 1984, 40, 2935.
    • (1984) Tetrahedron , vol.40 , pp. 2935
    • Kitahara, T.1    Mori, K.2
  • 8
    • 0028349304 scopus 로고
    • Reference 1 has shown elegant elaboration of hydroxyheptenyl chain of brefeldin A followed by cyclopentane construction
    • f) Miyaoka, H.; Kajiwara, M. J. Chem. Soc. Chem. Commun. 1994, 483. Reference 1 has shown elegant elaboration of hydroxyheptenyl chain of brefeldin A followed by cyclopentane construction.
    • (1994) J. Chem. Soc. Chem. Commun. , pp. 483
    • Miyaoka, H.1    Kajiwara, M.2
  • 11
    • 0000513405 scopus 로고
    • 5. Drian, C. L.; Greene, A. E. J. Am. Chem. Soc. 1982, 104, 5473. Nokami, J.; Ohkura, M.; Dan-Oh, Y.; Sakamoto, Y. Tetrahedron Lett. 1991, 32, 2409. The known 6-silyloxy-1-heptyne (6) was straightforwardly prepared from (S)-lactate in 74 % overall yield by our own six step sequence. (equition presented)
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5473
    • Drian, C.L.1    Greene, A.E.2
  • 12
    • 0025854913 scopus 로고
    • The known 6-silyloxy-1-heptyne (6) was straightforwardly prepared from (S)-lactate in 74 % overall yield by our own six step sequence. (equition presented)
    • 5. Drian, C. L.; Greene, A. E. J. Am. Chem. Soc. 1982, 104, 5473. Nokami, J.; Ohkura, M.; Dan-Oh, Y.; Sakamoto, Y. Tetrahedron Lett. 1991, 32, 2409. The known 6-silyloxy-1-heptyne (6) was straightforwardly prepared from (S)-lactate in 74 % overall yield by our own six step sequence. (equition presented)
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2409
    • Nokami, J.1    Ohkura, M.2    Dan-Oh, Y.3    Sakamoto, Y.4
  • 13
    • 0010500862 scopus 로고    scopus 로고
    • note
    • 2, vi) Litium acetylide-EDA complex, DMSO, 81% for 2steps
  • 14
    • 0010420714 scopus 로고    scopus 로고
    • note
    • 2).
  • 19
    • 49549126692 scopus 로고
    • 11. Unpublished results. The details for this extremely mild desulfonylation procedure will be reported soon in due courses. For Trost's conditions, see; Trost, B. M.; Arndt, H. C.; Strege, P. E.; Verhoeven, T. R. Tetrahedron Lett. 1976, 39, 3477.
    • (1976) Tetrahedron Lett. , vol.39 , pp. 3477
    • Trost, B.M.1    Arndt, H.C.2    Strege, P.E.3    Verhoeven, T.R.4
  • 20
    • 0010421418 scopus 로고    scopus 로고
    • DIBAL reduction of bicyclic lactone 12 provided the hydroxy aldehyde rather than lactol
    • 12. DIBAL reduction of bicyclic lactone 12 provided the hydroxy aldehyde rather than lactol.
  • 21
    • 0010503295 scopus 로고    scopus 로고
    • note
    • 2).
  • 22
    • 0002339617 scopus 로고
    • 14. Corey, E. J.; Wellenberg, R. H. Tetrahedron Lett. 1976, 4705. Honda, M.; Hirata, K.; Sueoka, H.; Katsuki, T.; Yamaguchi, M. Tetrahedron Lett. 1981, 22, 2679.
    • (1976) Tetrahedron Lett. , pp. 4705
    • Corey, E.J.1    Wellenberg, R.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.