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Volumn 121, Issue 2, 1999, Pages 456-457

Enantioselective total synthesis of reveromycin B

Author keywords

[No Author keywords available]

Indexed keywords

NATURAL PRODUCT; REVEROMYCIN B; UNCLASSIFIED DRUG;

EID: 0033585536     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja983429n     Document Type: Article
Times cited : (49)

References (24)
  • 1
    • 0026020228 scopus 로고
    • Osada, H.; Koshino, H.; Isono, K.; Takahashi, H.; Kawanishi, G. J. Antibiot. 1991, 44, 259. Koshino, H.; Takahashi, H.; Osada, H.; Isono, K. J. Antibiotics 1992, 45, 1420. Takahashi, H.; Osada, H.; Koshino, H.; Kudo, T.; Amano, S.; Shimizu, S.; Yoshihama, M.; Isono, K. J. Antibiot. 1992, 45, 1409.
    • (1991) J. Antibiot. , vol.44 , pp. 259
    • Osada, H.1    Koshino, H.2    Isono, K.3    Takahashi, H.4    Kawanishi, G.5
  • 2
    • 0026764947 scopus 로고
    • Osada, H.; Koshino, H.; Isono, K.; Takahashi, H.; Kawanishi, G. J. Antibiot. 1991, 44, 259. Koshino, H.; Takahashi, H.; Osada, H.; Isono, K. J. Antibiotics 1992, 45, 1420. Takahashi, H.; Osada, H.; Koshino, H.; Kudo, T.; Amano, S.; Shimizu, S.; Yoshihama, M.; Isono, K. J. Antibiot. 1992, 45, 1409.
    • (1992) J. Antibiotics , vol.45 , pp. 1420
    • Koshino, H.1    Takahashi, H.2    Osada, H.3    Isono, K.4
  • 11
    • 0000610844 scopus 로고
    • Kishi Y. Pure Appl. Chem. 1992, 64, 343. Cintas, P. Synthesis 1992, 248.
    • (1992) Pure Appl. Chem. , vol.64 , pp. 343
    • Kishi, Y.1
  • 12
    • 0026607521 scopus 로고
    • Kishi Y. Pure Appl. Chem. 1992, 64, 343. Cintas, P. Synthesis 1992, 248.
    • (1992) Synthesis , pp. 248
    • Cintas, P.1
  • 13
    • 0344139404 scopus 로고    scopus 로고
    • note
    • All new compounds exhibited satisfactory spectral and exact mass data. Yields refer to spectroscopically and chromatographically homogeneous materials.
  • 14
    • 0344139403 scopus 로고    scopus 로고
    • note
    • Experimental details for the synthesis of 3, 6, and 7 are included in Supporting Information.
  • 18
    • 0030743260 scopus 로고    scopus 로고
    • Panek, J. S.; Hu, T. J. Org. Chem. 1997, 62, 4912. Panek, J. S.; Hu, T. J. Org. Chem. 1997, 62, 4914.
    • (1997) J. Org. Chem. , vol.62 , pp. 4912
    • Panek, J.S.1    Hu, T.2
  • 19
    • 0030790367 scopus 로고    scopus 로고
    • Panek, J. S.; Hu, T. J. Org. Chem. 1997, 62, 4912. Panek, J. S.; Hu, T. J. Org. Chem. 1997, 62, 4914.
    • (1997) J. Org. Chem. , vol.62 , pp. 4914
    • Panek, J.S.1    Hu, T.2
  • 20
    • 0345433036 scopus 로고    scopus 로고
    • note
    • Our earlier attempts to exploit Stille cross-coupling chemistry for this transformation proved to be either unsuccessful or produced 15 in low yields.
  • 22
    • 84985080215 scopus 로고
    • Sieber, P. Helv. Chim. Acta 1977, 60, 2711. Lipshutz, B. H.; Miller, T. A. Tetrahedron Lett. 1989, 30, 7149.
    • (1977) Helv. Chim. Acta , vol.60 , pp. 2711
    • Sieber, P.1
  • 24
    • 0344570912 scopus 로고    scopus 로고
    • note
    • We thank Professor H. Osada (RIKEN Institute, Japan) for providing us with the NMR data of natural reveromycin B.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.