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Volumn 135, Issue 1, 2013, Pages 58-61

N-heterocyclic carbene-catalyzed Ireland-Coates claisen rearrangement: Synthesis of functionalized β-lactones

Author keywords

[No Author keywords available]

Indexed keywords

CLAISEN REARRANGEMENT; DIASTEREO-SELECTIVITY; DIVERSE RANGE; FUNCTIONALIZED; MECHANISTIC STUDIES; N-HETEROCYCLIC; N-HETEROCYCLIC CARBENES; STEREOSELECTIVE SYNTHESIS;

EID: 84872112660     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja310449k     Document Type: Article
Times cited : (151)

References (56)
  • 46
    • 82455205867 scopus 로고    scopus 로고
    • The role of salts in NHC organocatalysis has been documented previously by us and others. For cooperative catalysis using Lewis acids and nucleophilic carbenes, see: Cohen, D. T.; Scheidt, K. A. Chem. Sci. 2012, 3, 53 and references therein
    • (2012) Chem. Sci. , vol.3 , pp. 53
    • Cohen, D.T.1    Scheidt, K.A.2
  • 54
    • 0000204523 scopus 로고
    • The role of the counterion in the anionic Cope rearrangement is documented in Evans' seminal communication: Evans, D. A.; Golub, A. M. J. Am. Chem. Soc. 1975, 97, 4765
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 4765
    • Evans, D.A.1    Golub, A.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.