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Volumn 11, Issue 17, 2005, Pages 4935-4952

Solution- and solid-phase synthesis of radicicol (monorden) and pochonin C

Author keywords

Metathesis; Natural products; Solid phase synthesis; Total synthesis

Indexed keywords

ALCOHOLS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC POLYMERS;

EID: 24344442417     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200500160     Document Type: Article
Times cited : (60)

References (56)
  • 21
    • 0037451452 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 1280-1284.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1280-1284
  • 30
    • 4544334262 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3467-3470.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3467-3470
  • 39
    • 24344502270 scopus 로고    scopus 로고
    • note
    • A survey of the literature revealed that most Mitsunobu esterifica-tion on 2-hydroxybenzoic acid were carried out with the hydroxy group in the 2-position left unprotected. The benefit of this free phenol presumably comes from the hydrogen bond it forms with the acid thereby increasing the acidity of the benzoic acid which is known to accelerate the reaction.
  • 54
    • 24344433504 scopus 로고    scopus 로고
    • note
    • Synthetic pochonin C was found to have identical NMR spectra to natural pochonin D (spectra were kindly provide by Marc Stadler, Bayer Health Care, Wuppertal, Germany).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.