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Volumn 47, Issue 22, 2006, Pages 3755-3757

The first total synthesis of lamellarin α 20-sulfate, a selective inhibitor of HIV-1 integrase

Author keywords

Hinsberg reaction; HIV 1 integrase inhibitor; Lamellarin; Sulfate; Suzuki Miyaura coupling

Indexed keywords

BENZYL DERIVATIVE; INTEGRASE INHIBITOR; LAMELLARIN ALPHA 20 SULFATE; PYRROLE; UNCLASSIFIED DRUG;

EID: 33646102443     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.03.121     Document Type: Article
Times cited : (95)

References (26)
  • 1
    • 0042423356 scopus 로고    scopus 로고
    • For a review of HIV-1 integrase inhibitors, see:
    • For a review of HIV-1 integrase inhibitors, see:. Maurin C., Bailly F., and Cotelle P. Curr. Med. Chem. 10 (2003) 1795-1810
    • (2003) Curr. Med. Chem. , vol.10 , pp. 1795-1810
    • Maurin, C.1    Bailly, F.2    Cotelle, P.3
  • 14
    • 23944462404 scopus 로고    scopus 로고
    • During the course of our synthesis of lamellarin α 20-sulfate (1), Fürstner completed the total synthesis of the marine alkaloid dictyodendrin B, in which Taylor's protocol was successfully used for the final sulfate formation, see:
    • During the course of our synthesis of lamellarin α 20-sulfate (1), Fürstner completed the total synthesis of the marine alkaloid dictyodendrin B, in which Taylor's protocol was successfully used for the final sulfate formation, see:. Fürstner A., Domostoj M.M., and Scheiper B. J. Am. Chem. Soc. 127 (2005) 11620-11621
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 11620-11621
    • Fürstner, A.1    Domostoj, M.M.2    Scheiper, B.3
  • 19
    • 33646094149 scopus 로고    scopus 로고
    • note
    • The boronic acid 11 was prepared from O-benzylisovanillin in a similar manner as described for the synthesis of 4-isopropoxy-5-methoxy-2-methoxymethoxyphenylboronic acid. See Ref. 10.
  • 26
    • 33646082442 scopus 로고    scopus 로고
    • note
    • -]: 592.0914. Found: 592.0913.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.