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Volumn 24, Issue 20, 2013, Pages 2720-2722

Indirect support for a stepwise carbonium ion pathway operating in (4+3)-cycloaddition reactions between furanoxonium ions and 1,3-dienes

Author keywords

(4+3) type cycloadditions; furanoxonium ions; furfuryl alcohols

Indexed keywords

1,3 DIENE DERIVATIVE; ALKADIENE; CARBONIUM ION; CYCLOHEPTENE; CYCLOHEXA 1,3 DIENE; CYCLOPENTADIENE; DICHLOROMETHANE METHANOL; FURANOXONIUM ION; FURFURYL ALCOHOL; ION; METHANOL DERIVATIVE; PLUMARELLIDE; RAMESWARALIDE; SUBSTITUTED FURYL TETRAHYDROFURAN DERIVATIVE; TETRAHYDROFURAN DERIVATIVE; TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG;

EID: 84885336390     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0033-1339893     Document Type: Article
Times cited : (13)

References (11)
  • 1
    • 7444242717 scopus 로고    scopus 로고
    • For illustrations of the scope for the products of oxidative cleavage of the furan ring in furfuryl alcohols, i.e. the Achmatowicz reaction, in synthesis, see: and references therein
    • For illustrations of the scope for the products of oxidative cleavage of the furan ring in furfuryl alcohols, i.e., the Achmatowicz reaction, in synthesis, see: Burke M. D., Berger E. M., Schreiber S. L. J. Am. Chem. Soc.: 2004; 126 14095; and references therein
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 14095
    • Burke, M.D.1    Berger, E.M.2    Schreiber, S.L.3
  • 2
    • 70350020774 scopus 로고    scopus 로고
    • For recent examples of the scope for [5+2]-cycloaddition reactions in synthesis, including natural products, see: and references therein
    • For recent examples of the scope for [5+2]-cycloaddition reactions in synthesis, including natural products, see: Tang B., Bray C. D., Pattenden G. Org. Biomol. Chem.: 2009; 7 4448; and references therein
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 4448
    • Tang, B.1    Bray, C.D.2    Pattenden, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.