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Volumn 48, Issue 24, 2007, Pages 4259-4262

Synthesis of the C1-C12 fragment of amphidinolide T1

Author keywords

Amphidinolide; Cross metathesis; Evans' aldol; Oxy Michael

Indexed keywords

AMPHIDINOLIDE T1; MACROLIDE; UNCLASSIFIED DRUG;

EID: 34248578624     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.04.069     Document Type: Article
Times cited : (17)

References (33)
  • 1
    • 0000138888 scopus 로고    scopus 로고
    • For a review on the isolation of the amphidinolides, see:. Mori K. (Ed), Elsevier, New York
    • For a review on the isolation of the amphidinolides, see:. Kobayashi J. In: Mori K. (Ed). Comprehensive Natural Products Chemistry Vol. 8 (1999), Elsevier, New York 619
    • (1999) Comprehensive Natural Products Chemistry , vol.8 , pp. 619
    • Kobayashi, J.1
  • 5
    • 0037420318 scopus 로고    scopus 로고
    • For total syntheses of amphidinolide T1, see:
    • For total syntheses of amphidinolide T1, see:. Ghosh A.K., and Liu C. J. Am. Chem. Soc. 125 (2003) 2374
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2374
    • Ghosh, A.K.1    Liu, C.2
  • 12
    • 0033597805 scopus 로고    scopus 로고
    • For recent examples of the oxy-Michael reaction, see:
    • For recent examples of the oxy-Michael reaction, see:. Honda T., and Ishikawa F. J. Org. Chem. 64 (1999) 5542
    • (1999) J. Org. Chem. , vol.64 , pp. 5542
    • Honda, T.1    Ishikawa, F.2
  • 15
    • 33746087596 scopus 로고    scopus 로고
    • Base mediated epimerisation based on a ring-opening/ring-closure mechanism cannot be ruled out, see:
    • Base mediated epimerisation based on a ring-opening/ring-closure mechanism cannot be ruled out, see:. Freifeld I., Holtz E., Dahmann G., and Langer P. Eur. J. Org. Chem. (2006) 3251
    • (2006) Eur. J. Org. Chem. , pp. 3251
    • Freifeld, I.1    Holtz, E.2    Dahmann, G.3    Langer, P.4
  • 16
    • 34248558590 scopus 로고    scopus 로고
    • note
    • The stereochemistry was determined by NOE experiments.
  • 20
    • 18744394355 scopus 로고    scopus 로고
    • For some recent examples, see:
    • For some recent examples, see:. Bellur E., and Langer P. J. Org. Chem. 70 (2005) 3819
    • (2005) J. Org. Chem. , vol.70 , pp. 3819
    • Bellur, E.1    Langer, P.2
  • 25
    • 0009802446 scopus 로고
    • Isomerisation of Z to E configuration of 2-alkylidenetetrahydrofurans is well documented in literature, see:
    • Isomerisation of Z to E configuration of 2-alkylidenetetrahydrofurans is well documented in literature, see:. Batmangherlich S., and Davidson A.H. Tetrahedron Lett. 24 (1983) 2889
    • (1983) Tetrahedron Lett. , vol.24 , pp. 2889
    • Batmangherlich, S.1    Davidson, A.H.2
  • 30
    • 34248555081 scopus 로고    scopus 로고
    • Ref. 11c.
  • 33
    • 34248560566 scopus 로고    scopus 로고
    • note
    • 4SiNa 395.2589.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.