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Volumn 71, Issue 2, 2006, Pages 498-503

Synthesis and reactivity of new chiral bicyclic phospholanes as acyl-transfer catalysts

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; CATALYSTS; COMPUTATIONAL METHODS; GROUND STATE; MOLECULAR STRUCTURE; QUENCHING; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 30744459136     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0519155     Document Type: Article
Times cited : (48)

References (33)
  • 11
    • 1842305809 scopus 로고
    • Kochi, J. K., Ed.; Wiley: New York
    • Bentrude, W. G. In Free radicals; Kochi, J. K., Ed.; Wiley: New York, 1973; Vol. 2, pp 595-663.
    • (1973) Free Radicals , vol.2 , pp. 595-663
    • Bentrude, W.G.1
  • 21
    • 0035944472 scopus 로고    scopus 로고
    • For a related nonradical approach for the formation of five-membered cyclic phosphines, see: Douglas, M. R.; Stern, C. L.; Marks, T. J. J. Am. Chem. Soc. 2001, 123, 10221.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 10221
    • Douglas, M.R.1    Stern, C.L.2    Marks, T.J.3
  • 24
    • 30744449203 scopus 로고    scopus 로고
    • note
    • (a) We have not determined whether 8a is formed under kinetic or thermodynamic control. Formation of the more stable phosphorus configuration 8a would be no surprise in a kinetically controlled cyclization. However, reversible phosphinyl radical additions are precedented and would also be expected to lead to 8a.
  • 31
    • 0033921576 scopus 로고    scopus 로고
    • For recent reviews on the kinetic resolution of alcohols using chiral nucleophilic catalysts, see: (a) Fu, G. C. Acc. Chem. Res. 2000, 33, 412.
    • (2000) Acc. Chem. Res. , vol.33 , pp. 412
    • Fu, G.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.