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Volumn 49, Issue 45, 2008, Pages 6462-6465

Total synthesis of (-)-centrolobine

Author keywords

2,6 syn Tetrahydropyran; Butyllithium; CBS reduction; Cyclization; Mitsunobu reaction

Indexed keywords

ACETAL DERIVATIVE; ANTILEISHMANIAL AGENT; CENTROLOBINE; LEWIS ACID; LITHIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 52049089162     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.08.102     Document Type: Article
Times cited : (45)

References (47)
  • 28
    • 52049096247 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess (ee) was determined by HPLC (Daicel Chiralcel OD-H, 2-propanol/n-hexane = 1:15).
  • 32
    • 0346324621 scopus 로고
    • For intramolecual Barbier-type reaction of iodo-esters with organolithiums, see:
    • For intramolecual Barbier-type reaction of iodo-esters with organolithiums, see:. Cooke Jr. M.P., and Houpis I.N. Tetrahedron Lett. 26 (1985) 4987-4990
    • (1985) Tetrahedron Lett. , vol.26 , pp. 4987-4990
    • Cooke Jr., M.P.1    Houpis, I.N.2
  • 44
    • 52049093284 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess (ee) was determined by HPLC analysis (Daicel Chiralpak AD-H, 2-propanol/n-hexane = 1:15).
  • 45
    • 52049107213 scopus 로고    scopus 로고
    • note
    • +) 335.1618, found 335.1618.
  • 46
    • 52049111061 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess (ee) was determined by HPLC analysis (Daicel Chiralcel OD-H, 2-propanol/n-hexane = 1:99).
  • 47
    • 52049099695 scopus 로고    scopus 로고
    • note
    • 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.