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Volumn 128, Issue 13, 2006, Pages 4232-4233

Asymmetric Claisen rearrangements enabled by catalytic asymmetric Di(allyl) ether synthesis

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; DIMETHYL ETHER; ETHER DERIVATIVE;

EID: 33645470784     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja058172p     Document Type: Article
Times cited : (63)

References (24)
  • 6
    • 0000956817 scopus 로고
    • Other examples olefin isomerization-Claisen rearrangements: (a) Reuter, J. M.; Salomon, R. G. J. Org. Chem. 1977, 42, 3360.
    • (1977) J. Org. Chem. , vol.42 , pp. 3360
    • Reuter, J.M.1    Salomon, R.G.2
  • 12
    • 33845279007 scopus 로고
    • and references therein
    • Ziegler, F. E. Chem. Rev. 1988, 88, 1423 and references therein.
    • (1988) Chem. Rev. , vol.88 , pp. 1423
    • Ziegler, F.E.1
  • 13
    • 0012677208 scopus 로고    scopus 로고
    • For the development of Pd(0)-catalyzed allylation of symmetric zinc alkoxides, see: Kim, H.; Lee, C. Org. Lett. 2002, 4, 4369.
    • (2002) Org. Lett. , vol.4 , pp. 4369
    • Kim, H.1    Lee, C.2
  • 15
    • 33645464569 scopus 로고    scopus 로고
    • note
    • The illustrated structures for zinc alkoxides 3 and 5 are based on reagent stoichiometry; 3 and 5 were not rigorously characterized.
  • 16
    • 33645473380 scopus 로고    scopus 로고
    • note
    • Claisen adduct 9 is accompanied by a considerable amount of unreacted di(allyl) ether due to sluggish isomerization of the sterically hindered vinyl silane moiety.
  • 18
    • 0037120811 scopus 로고    scopus 로고
    • For MIB-catalyzed additions of in situ generated vinyl zinc reagents to benzaldehyde, see: (a) Chen, Y. K.; Lurain, A. E.; Walsh, P. J. J. Am. Chem. Soc. 2002, 124, 12225.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 12225
    • Chen, Y.K.1    Lurain, A.E.2    Walsh, P.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.