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Volumn 4, Issue 7, 2002, Pages 1239-1241

Lewis Acid Promoted Phenylseleno Group Transfer Tandem Radical Cyclization Reactions

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EID: 0042375996     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol025750n     Document Type: Article
Times cited : (29)

References (31)
  • 6
    • 0006557011 scopus 로고    scopus 로고
    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim Chapter 1.5
    • (f) For a recent review, see: Byers, J. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1, Chapter 1.5.
    • (2001) Radicals in Organic Synthesis , vol.1
    • Byers, J.1
  • 8
    • 0032538355 scopus 로고    scopus 로고
    • For an recent review on the use of Lewis acids in free radical reactions, see: (a) Renaud, P.; Gerster, M. Angew. Chem., Int. Ed. 1998, 37, 2562-2579. For recent examples of Lewis acid promoted atom transfer radical reactions, see:
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 2562-2579
    • Renaud, P.1    Gerster, M.2
  • 22
    • 0041400800 scopus 로고    scopus 로고
    • note
    • 2 was used as the Lewis acid, the addition of 4 Å molecular sieves led to faster reaction and higher yield
  • 31
    • 0032960346 scopus 로고    scopus 로고
    • For an excellent review on enantioselective radical reactions, see: Sibi, M. P.; Porter, N. A. Acc. Chem. Res. 1999, 32, 163-171.
    • (1999) Acc. Chem. Res. , vol.32 , pp. 163-171
    • Sibi, M.P.1    Porter, N.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.