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Volumn 49, Issue 24, 2008, Pages 3899-3901

A highly enantioselective synthesis of (-)- and (+)-juglomycin A through Dötz annulation and asymmetric dihydroxylation

Author keywords

Asymmetric dihydroxylation; Asymmetric synthesis; D tz annulation; Juglomycins; Modified Knoevenagel reaction

Indexed keywords

ANTIBIOTIC AGENT; JUGLOMYCIN A; JUGLOMYCIN B;

EID: 43049168648     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.04.059     Document Type: Article
Times cited : (26)

References (20)
  • 9
    • 0002961432 scopus 로고
    • Method: Using methyl malonate:
    • Method: Using methyl malonate:. Ragoussis N. Tetrahedron Lett. 28 (1987) 93
    • (1987) Tetrahedron Lett. , vol.28 , pp. 93
    • Ragoussis, N.1
  • 14
    • 33644560625 scopus 로고    scopus 로고
    • Alkyne 5 was prepared by TBDMS protection of commercially available 3-butyn-1-ol as reported earlier:
    • Alkyne 5 was prepared by TBDMS protection of commercially available 3-butyn-1-ol as reported earlier:. Narayan R.S., and Borhan B. J. Org. Chem. 71 (2006) 1416
    • (2006) J. Org. Chem. , vol.71 , pp. 1416
    • Narayan, R.S.1    Borhan, B.2
  • 19
    • 43049166060 scopus 로고    scopus 로고
    • note
    • 11 The spectroscopic and analytical data of ent-10 were similar to 10.
  • 20
    • 19944417918 scopus 로고    scopus 로고
    • Enantiomeric excess (ee) was determined by chiral HPLC as reported:
    • Enantiomeric excess (ee) was determined by chiral HPLC as reported:. Fernandes R.A., and Brückner R. Synlett (2005) 1281
    • (2005) Synlett , pp. 1281
    • Fernandes, R.A.1    Brückner, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.