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Volumn 350, Issue 1, 2008, Pages 40-42

Brønsted acid-catalyzed synthesis of pyrans via a formal [3+3] cycloaddition

Author keywords

, unsatu Rated carbonyl compounds; Cycloaddition; Electrocyclic reactions; Organocatalysis; Oxygen heterocycles

Indexed keywords


EID: 38349159602     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200700375     Document Type: Article
Times cited : (47)

References (36)
  • 1
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    • For recent reviews on the reactivity of 1,3-dicarbonyl compounds: a
    • For recent reviews on the reactivity of 1,3-dicarbonyl compounds: a) C. Simon, T. Constantieux, J. Rodriguez, Eur. J. Org. Chem. 2004, 4957;
    • (2004) Eur. J. Org. Chem , pp. 4957
    • Simon, C.1    Constantieux, T.2    Rodriguez, J.3
  • 4
    • 0028810949 scopus 로고    scopus 로고
    • For some examples of the MARDI cascade: a M.-H. Filippini, R. Faure, J. Rodriguez, J. Org. Chem. 1995, 60, 6872;
    • For some examples of the MARDI cascade: a) M.-H. Filippini, R. Faure, J. Rodriguez, J. Org. Chem. 1995, 60, 6872;
  • 11
    • 30744456247 scopus 로고    scopus 로고
    • For a recent review on application of electrocyclization reactions in synthesis, see: a
    • For a recent review on application of electrocyclization reactions in synthesis, see: a) C. M. Beaudry, J. P. Malerich, D. Trauner, Chem. Rev. 2005, 105, 4757;
    • (2005) Chem. Rev , vol.105 , pp. 4757
    • Beaudry, C.M.1    Malerich, J.P.2    Trauner, D.3
  • 35
    • 38349159032 scopus 로고    scopus 로고
    • 2, the yields were lower.
    • 2, the yields were lower.
  • 36
    • 38349094550 scopus 로고    scopus 로고
    • The relative stereochemistry of the major diastereomer of 1k was determined by nOe experiment.
    • The relative stereochemistry of the major diastereomer of 1k was determined by nOe experiment.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.