메뉴 건너뛰기




Volumn 20, Issue 19, 2009, Pages 2216-2219

Asymmetric synthesis of aza-diospongin A as an iNOS inducer

Author keywords

[No Author keywords available]

Indexed keywords

1 (AZIDOBUT 3 ENYL)BENZENE; 2 4 HYDROXY 6 PHENYLPIPERIDIN 2 YL) 1 PHENYLETHANONE; ALKENE; ALLYL ALCOHOL; DIOSPONGIN A; DIOSPONGIN B; INDUCIBLE NITRIC OXIDE SYNTHASE; NITRIC OXIDE SYNTHASE; NITRITE; PIPERIDINE; TERT BUTYL 1 PHENYLBUT 3 ENYLCARBAMATE; TERT BUTYL 3 HYDROXY 7 OXO 1,7 DIPHENYL HEPT 5 ENYLCARBAMATE; TERT BUTYL 3 HYDROXYL 1 PHENYLHEX 5 ENYLCARBAMATE; UNCLASSIFIED DRUG;

EID: 72049119638     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.09.013     Document Type: Article
Times cited : (16)

References (29)
  • 23
    • 32144461395 scopus 로고    scopus 로고
    • Compound 9 was prepared from benzaldehyde in two steps: addition of vinyl magnesium bromide followed by IBX oxidation. See ref:
    • Compound 9 was prepared from benzaldehyde in two steps: addition of vinyl magnesium bromide followed by IBX oxidation. See ref:. Wu F., Li H., Hong R., and Deng L. Angew. Chem., Int. Ed. 45 (2006) 947
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 947
    • Wu, F.1    Li, H.2    Hong, R.3    Deng, L.4
  • 24
    • 72049095224 scopus 로고    scopus 로고
    • note
    • Enantiomeric excess was determined by chiral HPLC with chiral column: OD-H, 250 × 4.6 mm, 5 μm; mobile phase: 30% i-propanol in hexanes; flow rate: 1 mL/min.; detection: PDA; run time: 30 min.; retention time: 6.5.
  • 25
    • 72049124444 scopus 로고    scopus 로고
    • note
    • NOE experiment has been carried out on aza-diospongin-A 2 and key NOE enhancements are shown below.{A figure is presented}


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.