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Volumn 5, Issue 14, 2003, Pages 2425-2428

Stereoselective trimerization of [(S)R]-[(p-tolylsulfinyl)methyl] -p-quinols and p-quinamines

Author keywords

[No Author keywords available]

Indexed keywords

4 QUINAMINE; [(4 TOLYLSULFINYL)METHYL] 4 QUINOL; ALCOHOL DERIVATIVE; AMINE; NITROGEN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0141743330     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol034589t     Document Type: Article
Times cited : (24)

References (25)
  • 1
    • 0034694720 scopus 로고    scopus 로고
    • Evidence supporting the real intermediacy of quinols in such biosynthetic routes has been recently reported: Abe, N.; Sugimoto, O.; Tanji, K.; Hirota, A. J. Am. Chem. Soc. 2000, 122, 12606-12607.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 12606-12607
    • Abe, N.1    Sugimoto, O.2    Tanji, K.3    Hirota, A.4
  • 15
    • 84978556575 scopus 로고
    • By analogy with p-quinols, we use the name p-quinamines for the 4-amino analogues. This name was proposed in 1928: Fries, K.; Ohemes, G. Justus Liebigs Ann Chem. 1928, 462, 1.
    • (1928) Justus Liebigs Ann Chem. , vol.462 , pp. 1
    • Fries, K.1    Ohemes, G.2
  • 20
    • 0000428270 scopus 로고    scopus 로고
    • p-Quinols are sufficiently stable to be isolated and stored. See, for instance: Wipf, P.; Jung, J.-K. Chem. Rev. 1999, 99, 1469-1480.
    • (1999) Chem. Rev. , vol.99 , pp. 1469-1480
    • Wipf, P.1    Jung, J.-K.2
  • 21
    • 0141665725 scopus 로고    scopus 로고
    • note
    • Conditions were chosen in accordance with previous results obtained with p-quinamine 2; see ref 9.
  • 22
    • 0141554252 scopus 로고    scopus 로고
    • note
    • 2 group instead of the alkoxide acting as nucleophile and with enols instead of enolates as intermediates due to the ethanolic medium.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.