메뉴 건너뛰기




Volumn 9, Issue 9, 2011, Pages 3516-3529

Enantioselective radical cyclisation reactions of 4-substituted quinolones mediated by a chiral template

Author keywords

[No Author keywords available]

Indexed keywords

CHIRAL TEMPLATES; CYCLISATIONS; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE; ENANTIOSELECTIVE RADICALS; GOOD YIELD; NMR TITRATION; NON-LINEARITY; QUINOLONES; RADICAL CYCLISATION; REDUCTION PRODUCTS;

EID: 79954444640     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0ob01272f     Document Type: Article
Times cited : (43)

References (82)
  • 3
    • 0004269715 scopus 로고    scopus 로고
    • P. Renaud and M. P. Sibi (ed.), VCH, Weinheim
    • P. Renaud, and, M. P. Sibi, (ed.), Radicals in Organic Synthesis, VCH, Weinheim, 2001
    • (2001) Radicals in Organic Synthesis
  • 10
    • 0004269715 scopus 로고    scopus 로고
    • P. Renaud and M. P. Sibi, ed., VCH, Weinheim, 416
    • Reviews: N A. Porter in Radicals in Organic Synthesis,, P. Renaud, and, M. P. Sibi,, ed., VCH, Weinheim, 2001, Vol. 1, 416
    • (2001) Radicals in Organic Synthesis
    • Porter, N.A.1
  • 20
  • 30
    • 84886330800 scopus 로고    scopus 로고
    • For a pertinent review on asymmetric catalysis by chiral hydrogen-bond donors
    • D. O. Jang S. Y. Kim J. Am. Chem. Soc. 2008 130 16152
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 16152
    • Jang, D.O.1    Kim, S.Y.2
  • 76
    • 0034682859 scopus 로고    scopus 로고
    • HOSTEST 5.6, program by C. S. Wilcox, N. M. Glagovich, University of Pittsburgh Dr. John M. Sanderson, Durham University, is acknowledged for making this tool available:
    • L. Fielding Tetrahedron 2000 56 6151
    • (2000) Tetrahedron , vol.56 , pp. 6151
    • Fielding, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.