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Volumn 128, Issue 16, 2006, Pages 5356-5357

Development of the 1,2-oxaza-cope rearrangement

Author keywords

[No Author keywords available]

Indexed keywords

COORDINATION COMPOUND; FUNCTIONAL GROUP; LEWIS ACID; NITROSO DERIVATIVE; OXAZINE DERIVATIVE;

EID: 33646464701     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0609710     Document Type: Article
Times cited : (26)

References (33)
  • 1
    • 0030866295 scopus 로고    scopus 로고
    • For a review, see: Paquette, L. A. Tetrahedron 1997, 53, 13971-14020.
    • (1997) Tetrahedron , vol.53 , pp. 13971-14020
    • Paquette, L.A.1
  • 2
    • 0001626504 scopus 로고
    • For leading references and reviews, see: (a) Overman, L. E. Acc. Chem. Res. 1992, 25, 352-359.
    • (1992) Acc. Chem. Res. , vol.25 , pp. 352-359
    • Overman, L.E.1
  • 6
    • 0037161886 scopus 로고    scopus 로고
    • There is an isolated yet intriguing example of a [3,3]-sigmatropic shift involving the nitro group that proceeds in the reverse direction: Wade, P. A.; Murray, J. K., Jr.; Shah-Patel, S.; Le, H. T. Chem. Commun. 2002, 1090.
    • (2002) Chem. Commun. , pp. 1090
    • Wade, P.A.1    Murray Jr., J.K.2    Shah-Patel, S.3    Le, H.T.4
  • 7
    • 0027495999 scopus 로고
    • For applications of oxazines in synthesis, see: (a) Keck, G. E.; Romer, D. R. J. Org. Chem. 1993, 58, 6083.
    • (1993) J. Org. Chem. , vol.58 , pp. 6083
    • Keck, G.E.1    Romer, D.R.2
  • 20
    • 0043032911 scopus 로고    scopus 로고
    • Limited information is available on π-facial selectivity in similar bicyclo-[2,2,2]oct-2-ene systems. For an excellent analysis of the topic, please see: (a) Paquette, L. A.; Guevel, R.; Sakamoto, S.; Kim, I. H.; Crawford, J. J. Org. Chem. 2003, 68, 6096.
    • (2003) J. Org. Chem. , vol.68 , pp. 6096
    • Paquette, L.A.1    Guevel, R.2    Sakamoto, S.3    Kim, I.H.4    Crawford, J.5
  • 23
    • 0001524266 scopus 로고
    • Although supported by the HRMS analysis, complete characterization of the byproducts arising from the other diastereomer is complicated by the possible existence of several stereoisomers of the dimeric nitroso esters. For a relevant discussion, see: Rogic, M. M.; Demmin, T. R.; Fuhrmann, R.; Koff, F. W. J. Am. Chem. Soc. 1975, 97, 3241.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 3241
    • Rogic, M.M.1    Demmin, T.R.2    Fuhrmann, R.3    Koff, F.W.4
  • 27
  • 32
    • 33646441166 scopus 로고    scopus 로고
    • note
    • See Supporting Information for the preparation of the substrates.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.