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Volumn , Issue 14 SPEC. ISS., 2008, Pages 2158-2162

A practical synthesis of the C1-C9 fragment of dictyostatin

Author keywords

Aldol reactions; Antitumor agents; Olefination; Stereoselective synthesis; Titanium

Indexed keywords

STEREOCHEMISTRY; STEREOSELECTIVITY;

EID: 48549094863     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067149     Document Type: Article
Times cited : (15)

References (38)
  • 25
    • 48549099174 scopus 로고    scopus 로고
    • Novartis AG, Annual Report, file no. 1-15024, Form 20-F, Jan 28, 2005, p 42.
    • Novartis AG, Annual Report, file no. 1-15024, Form 20-F, Jan 28, 2005, p 42.
  • 29
    • 0001316868 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon: Oxford
    • (b) Gennari, C. In Comprehensive Organic Synthesis, Vol. 2; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, 1991, 629.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 629
    • Gennari, C.1
  • 32
    • 48549094159 scopus 로고    scopus 로고
    • Hydrogenolysis with Pd/C in EtOAc at r.t. (see ref. 11c) resulted in concurrent extensive deprotection of the TBS groups.
    • (b) Hydrogenolysis with Pd/C in EtOAc at r.t. (see ref. 11c) resulted in concurrent extensive deprotection of the TBS groups.
  • 37
    • 0034725908 scopus 로고    scopus 로고
    • Olefination of an aldehyde similar to 12 by use of the Ando reagent gave the desired product as a Z/E mixture (9:1) in 70% yield: see ref. 6g. For the Ando reagent, see: Ando, K. J.; Oishi, T.; Hirama, M.; Ohno, H.; Ibuka, T. J. Org. Chem. 2000, 65, 4745.
    • Olefination of an aldehyde similar to 12 by use of the Ando reagent gave the desired product as a Z/E mixture (9:1) in 70% yield: see ref. 6g. For the Ando reagent, see: Ando, K. J.; Oishi, T.; Hirama, M.; Ohno, H.; Ibuka, T. J. Org. Chem. 2000, 65, 4745.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.