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Volumn , Issue 11, 1999, Pages 2991-2995

Asymmetric synthesis of the C1-C16 segment of lasonolide A

Author keywords

Macrocyclic factone; Marine natural products; Polyketide; Stereoselective carbonyl olefination

Indexed keywords

ANTINEOPLASTIC AGENT; LASONOLIDE A; UNCLASSIFIED DRUG;

EID: 0032742949     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(199911)1999:11<2991::aid-ejoc2991>3.3.co;2-q     Document Type: Article
Times cited : (22)

References (24)
  • 2
    • 0031562078 scopus 로고    scopus 로고
    • M. Nowakowski, H. M. R. Hoffmann, Tetrahedron Lett. 1997, 38, 1001. See also: M. K. Gurjar, A. Chakrabarti, B. V. Rao, P. Kumar, Tetrahedron Lett. 1997, 38, 6885; M. K. Gurjar, P. Kumar, B. V. Rao, Tetrahedron Lett. 1996, 37, 8617.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 1001
    • Nowakowski, M.1    Hoffmann, H.M.R.2
  • 3
    • 0030818229 scopus 로고    scopus 로고
    • M. Nowakowski, H. M. R. Hoffmann, Tetrahedron Lett. 1997, 38, 1001. See also: M. K. Gurjar, A. Chakrabarti, B. V. Rao, P. Kumar, Tetrahedron Lett. 1997, 38, 6885; M. K. Gurjar, P. Kumar, B. V. Rao, Tetrahedron Lett. 1996, 37, 8617.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6885
    • Gurjar, M.K.1    Chakrabarti, A.2    Rao, B.V.3    Kumar, P.4
  • 4
    • 16144365082 scopus 로고    scopus 로고
    • M. Nowakowski, H. M. R. Hoffmann, Tetrahedron Lett. 1997, 38, 1001. See also: M. K. Gurjar, A. Chakrabarti, B. V. Rao, P. Kumar, Tetrahedron Lett. 1997, 38, 6885; M. K. Gurjar, P. Kumar, B. V. Rao, Tetrahedron Lett. 1996, 37, 8617.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 8617
    • Gurjar, M.K.1    Kumar, P.2    Rao, B.V.3
  • 6
    • 0033118794 scopus 로고    scopus 로고
    • [3b] Discodermolide C1-C7 segment and Phorboxazole C20-C26 segment: A. Misske, H. M. R. Hoffmann, Tetrahedron 1999, 55, 4315.
    • (1999) Tetrahedron , vol.55 , pp. 4315
    • Misske, A.1    Hoffmann, H.M.R.2
  • 11
    • 85088333097 scopus 로고    scopus 로고
    • note
    • [2]
  • 13
    • 85088331971 scopus 로고    scopus 로고
    • note
    • [3a]
  • 14
    • 85088332068 scopus 로고    scopus 로고
    • note
    • [3b]
  • 17
    • 0002232935 scopus 로고    scopus 로고
    • A "racemic switch" has been defined as "the redevelopment in single-enantiomer form of a drug that was first approved as a racemate"; see: S. C. Stinson, Chem. Eng. News 1998, September 21, 83-104. In our case the early racemic switch provides two key single-isomer precursors of structurally different bioactive natural products.
    • (1998) Chem. Eng. News , vol.SEPTEMBER 21 , pp. 83-104
    • Stinson, S.C.1
  • 18
    • 25944457640 scopus 로고    scopus 로고
    • unpublished work
    • [8a] P. Schäfer, unpublished work.
    • Schäfer, P.1
  • 19
    • 25944460525 scopus 로고    scopus 로고
    • PhD thesis, in preparation
    • [8b] The ozonolysis was performed following a lead by: P. Schäfer, PhD thesis, in preparation.
    • Schäfer, P.1
  • 23
    • 0026325277 scopus 로고
    • 2Et was prepared according to the procedure recorded in: C. Patois, P. Savignac, Synth. Commun. 1991, 21, 2391.
    • (1991) Synth. Commun. , vol.21 , pp. 2391
    • Patois, C.1    Savignac, P.2
  • 24
    • 0344786972 scopus 로고    scopus 로고
    • note
    • The yield is 12% with respect to the early racemic switch rac-1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.