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Volumn 11, Issue 17, 2013, Pages 2847-2858

A stereoselective synthesis of the C9-C19 subunit of (+)-peloruside A

Author keywords

[No Author keywords available]

Indexed keywords

ANTI-TUMOR AGENTS; ASYMMETRIC TRANSFER HYDROGENATION; CHEMOENZYMATIC ROUTE; CONTROLLED REDUCTION; HYDROSTANNATION; REGIO-SELECTIVE; STEREOSELECTIVE SYNTHESIS; VINYLOGOUS MUKAIYAMA ALDOL REACTIONS;

EID: 84875861767     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob27508f     Document Type: Article
Times cited : (11)

References (56)
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  • 39
    • 0035917358 scopus 로고    scopus 로고
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    • Panek, J.S.1    Jain, N.F.2
  • 42
    • 84953502363 scopus 로고
    • 2 also failed to deliver 21 The outcome was no better in a less polar solvent like ether or toluene
    • J. I. Levin E. Turos S. M. Weinreb Synth. Commun. 1982 12 989
    • (1982) Synth. Commun. , vol.12 , pp. 989
    • Levin, J.I.1    Turos, E.2    Weinreb, S.M.3
  • 55
    • 0037467827 scopus 로고    scopus 로고
    • Probably as noted by Marshall and co-workers (ref. 37c), the secondary alcohol is probably not as effective as the primary alcohol in directing hydrostannation
    • J. A. Marshall M. P. Bourbeau Tetrahedron Lett. 2003 44 1087
    • (2003) Tetrahedron Lett. , vol.44 , pp. 1087
    • Marshall, J.A.1    Bourbeau, M.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.