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Volumn 10, Issue 5, 2008, Pages 957-960

Synthesis of an n-mesityl substituted chiral imidazolium salt for NHC-catalyzed reactions

Author keywords

[No Author keywords available]

Indexed keywords

DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; IMIDAZOLE DERIVATIVE; INORGANIC SALT;

EID: 43549123600     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol800006m     Document Type: Article
Times cited : (94)

References (32)
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    • For a recent, comprehensive review, see
    • For a recent, comprehensive review, see: Enders, D.; Niemeier, O.; Henseler, A. Chem. Rev. 2007, 107, 5606-5655.
    • (2007) Chem. Rev , vol.107 , pp. 5606-5655
    • Enders, D.1    Niemeier, O.2    Henseler, A.3
  • 2
    • 0038001592 scopus 로고    scopus 로고
    • For recent reviews, see: a
    • For recent reviews, see: (a) Johnson, J. S. Angew. Chem., Int. Ed. 2003, 42, 2534-2536.
    • (2003) Angew. Chem., Int. Ed , vol.42 , pp. 2534-2536
    • Johnson, J.S.1
  • 4
    • 3042770459 scopus 로고    scopus 로고
    • For the first reports of this concept, see: a
    • For the first reports of this concept, see: (a) Chow, K. Y.-C; Bode, J. W. J. Am. Chem. Soc. 2004,126, 8126-8127.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 8126-8127
    • Chow, K.Y.-C.1    Bode, J.W.2
  • 6
    • 28244479394 scopus 로고    scopus 로고
    • For a highlight, see
    • (c)For a highlight, see: Zeitler, K. Angew. Chem., Int. Ed. 2005, 44, 7506-7510.
    • (2005) Angew. Chem., Int. Ed , vol.44 , pp. 7506-7510
    • Zeitler, K.1
  • 21
    • 0037453328 scopus 로고    scopus 로고
    • For an excellent review of chiral N-heterocyclic carbenes, see
    • For an excellent review of chiral N-heterocyclic carbenes, see: Perry, M. C; Burgess, K. Tetrahedron: Asymmetry 2003, 14, 951-961.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 951-961
    • Perry, M.C.1    Burgess, K.2
  • 27
    • 58149192119 scopus 로고    scopus 로고
    • 4. Further details on the development of this route and its use to prepare a range of N- substituted derivatives is the subject of forthcoming full account.
    • 4. Further details on the development of this route and its use to prepare a range of N- substituted derivatives is the subject of forthcoming full account.
  • 28
    • 58149198167 scopus 로고    scopus 로고
    • The most common achiral imidazolium salt employed for homoeno-late based annulations is IMesCl
    • The most common achiral imidazolium salt employed for homoeno-late based annulations is IMesCl:
  • 29
    • 58149181956 scopus 로고    scopus 로고
    • 4 was employed. When DBU was used as base, the aldehyde was consumed but the dihydropyranone product was not observed.
    • 4 was employed. When DBU was used as base, the aldehyde was consumed but the dihydropyranone product was not observed.
  • 31
    • 34247874549 scopus 로고    scopus 로고
    • For another racemic variant, see
    • (b)For another racemic variant, see: Chan, A.; Scheidt, K. J. Am. Chem. Soc. 2007, 129, 5334-5335.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 5334-5335
    • Chan, A.1    Scheidt, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.