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Volumn 53, Issue 1, 2005, Pages 1-10

Total synthesis of the squalene synthase inhibitor zaragozic acid C

Author keywords

Aldol reaction; Carbonyl ylide cycloaddition; Internal ketalization; Olefin cross metathesis; Total synthesis; Zaragozic acid

Indexed keywords

6,7 DIDEOXYSQUALESTATIN H5; ESTER DERIVATIVE; NATURAL PRODUCT; SQUALENE SYNTHASE INHIBITOR; SQUALESTATIN; TARTARIC ACID; TARTARIC ACID DERIVATIVE; UNCLASSIFIED DRUG; ZARAGOZIC ACID A; ZARAGOZIC ACID C; ENZYME INHIBITOR; FUSED HETEROCYCLIC RINGS; SQUALENE SYNTHASE;

EID: 18744385558     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.53.1     Document Type: Review
Times cited : (20)

References (76)
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    • note
    • α-Keto ester 46 was prepared in 40% overall yield from diethyl L-tartrate by the eight-step sequence analogous to that illustrated for 41.
  • 49
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    • note
    • 38) carboxyl groups were introduced and/or protected as rert-butyl esters until the end of the synthesis.
  • 67
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    • note
    • 2Et, THF, -78 °C; (8) HMDS, imidazole, THF.
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    • note
    • 2.
  • 76
    • 0032864403 scopus 로고    scopus 로고
    • The strategy is, in principle, readily applicable to the synthesis of side chain congeners, and further efforts toward these goals are currently underway in our laboratory. For a preparation of the C6 acyl side chain of zaragozic acid A, see: Nakamura S., Inagaki J., Kitaguchi J., Tatani K., Hashimoto S., Chem. Pharm. Bull., 47, 1330-1333 (1999).
    • (1999) Chem. Pharm. Bull. , vol.47 , pp. 1330-1333
    • Nakamura, S.1    Inagaki, J.2    Kitaguchi, J.3    Tatani, K.4    Hashimoto, S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.