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Volumn 4, Issue 7, 2012, Pages 955-958

Asymmetric Organocatalysis Meets Hypervalent Iodine Chemistry for the α-Functionalization of Carbonyl Compounds

Author keywords

Asymmetric synthesis; Enantioselectivity; Hypervalent compounds; Iodine; Organocatalysis

Indexed keywords


EID: 84862730541     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201200116     Document Type: Note
Times cited : (54)

References (36)
  • 3
    • 77950261392 scopus 로고    scopus 로고
    • Ed.: B. List); Top. Curr. Chem. 291, Springer, Berlin, Germany
    • Asymmetric Organocatalysis (Ed.: B. List); Top. Curr. Chem. 291, Springer, Berlin, Germany, 2010.
    • (2010) Asymmetric Organocatalysis
  • 4
    • 84862728116 scopus 로고    scopus 로고
    • Ed.: M. Waser); Prog. Ch. Org. Nat. Prod., 96, Springer, Berlin, Germany
    • Asymmetric Organocatalysis in Natural Product Syntheses (Ed.: M. Waser); Prog. Ch. Org. Nat. Prod., 96, Springer, Berlin, Germany, 2012.
    • (2012) Asymmetric Organocatalysis in Natural Product Syntheses
  • 7
    • 79651474136 scopus 로고    scopus 로고
    • A subjective selection of recent examples is presented. The interested reader is encouraged to consult the primary literature or the following comprehensive review on the general use of hypervalent iodine reagents for the α-functionalization of carbonyls compounds
    • A subjective selection of recent examples is presented. The interested reader is encouraged to consult the primary literature or the following comprehensive review on the general use of hypervalent iodine reagents for the α-functionalization of carbonyls compounds: E. A. Merritt, B. Olofsson, Synthesis 2011, 517-538.
    • (2011) Synthesis , pp. 517-538
    • Merritt, E.A.1    Olofsson, B.2
  • 8
    • 84862735088 scopus 로고    scopus 로고
    • For a few selected examples, see:
    • For a few selected examples, see:
  • 18
    • 83455208461 scopus 로고    scopus 로고
    • For a review on the catalytic generation of hypervalent iodine reagents and hypoiodites, see:
    • H. Liang, M. A. Ciufolini, Angew. Chem. 2011, 123, 12051-12053; Angew. Chem. Int. Ed. 2011, 50, 11849-11851. For a review on the catalytic generation of hypervalent iodine reagents and hypoiodites, see:
    • (2011) Angew. Chem. 2011, 123, 12051-12053; Angew. Chem. Int. Ed. , vol.50 , pp. 11849-11851
    • Liang, H.1    Ciufolini, M.A.2
  • 28
    • 84862728121 scopus 로고    scopus 로고
    • For a few selected examples, see:
    • For a few selected examples, see:
  • 35
    • 84862729851 scopus 로고    scopus 로고
    • On-going investigations in our group have shown that optimisation of the catalyst and ester structures can lead to a substantial increase in the enantioselectivity of the reaction (up to 79%ee): D. Fernández González, J. Waser, unpublished results.
    • On-going investigations in our group have shown that optimisation of the catalyst and ester structures can lead to a substantial increase in the enantioselectivity of the reaction (up to 79%ee): D. Fernández González, J. Waser, unpublished results.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.