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Volumn 77, Issue 14, 2012, Pages 6358-6364

Julia-Kocienski reaction-based 1,3-diene synthesis: Aldehyde-dependent (E, E/E, Z)-selectivity

Author keywords

[No Author keywords available]

Indexed keywords

1 ,3-DIENES; CHELATING AGENT; DOUBLE BONDS; OLEFINATION REACTION;

EID: 84864035599     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo300929a     Document Type: Article
Times cited : (43)

References (23)
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    • In; Georg Thieme Verlag: Stuttgart, Vol. pp and references cited therein.
    • Markó, I. E.; Pospíšil, J. In Science of Synthesis; de Meijere, A., Ed.; Georg Thieme Verlag: Stuttgart, 2009; Vol. 47a, pp 105-160 and references cited therein.
    • (2009) Science of Synthesis , vol.47 , pp. 105-160
    • Markó, I.E.1    Pospíšil, J.2    De Meijere, A.3
  • 6
    • 70349213329 scopus 로고    scopus 로고
    • The addition/retroaddition process was already proposed previously as a possible explanation of unusual high (Z)-selectivity of newly created olefin; see
    • The addition/retroaddition process was already proposed previously as a possible explanation of unusual high (Z)-selectivity of newly created olefin; see: Kikuchi, R.; Fujii, M.; Akita, H. Tetrahedron: Asymmetry 2009, 20, 1975-1983
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1975-1983
    • Kikuchi, R.1    Fujii, M.2    Akita, H.3
  • 8
    • 0035974379 scopus 로고    scopus 로고
    • This assumption was based on analogy with the olefination reaction of 2-pyridyl sulfones with various aldehydes; see refs 1b, 4, and
    • This assumption was based on analogy with the olefination reaction of 2-pyridyl sulfones with various aldehydes; see refs 1b, 4, and: Charette, A. B.; Berthelette, C.; St-Martin, D. Tetrahedron Lett. 2001, 42, 5149-5153
    • (2001) Tetrahedron Lett. , vol.42 , pp. 5149-5153
    • Charette, A.B.1    Berthelette, C.2    St-Martin, D.3
  • 9
    • 79953199029 scopus 로고    scopus 로고
    • Allyl and benzyl BT- and PT-sulfones were prepared in two steps from the corresponding allylic or benzylic alcohols; see
    • Allyl and benzyl BT- and PT-sulfones were prepared in two steps from the corresponding allylic or benzylic alcohols; see: Pospíšil, J.; Sato, H. J. Org. Chem. 2011, 76, 2269-2272
    • (2011) J. Org. Chem. , vol.76 , pp. 2269-2272
    • Pospíšil, J.1    Sato, H.2
  • 10
    • 0000048258 scopus 로고
    • In; Trost, B. M. Fleming, I. Pergamon Press: Oxford, Vol.
    • Oppolzer, W. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 315-377.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 315-377
    • Oppolzer, W.1
  • 11
    • 0000048482 scopus 로고
    • In; Trost, B. M. Fleming, I. Pergamon Press: Oxford, Vol.
    • Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 513-546.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513-546
    • Roush, W.R.1
  • 12
    • 0000730407 scopus 로고
    • In; Trost, B. M. Fleming, I. Pergamon Press: Oxford, Vol.
    • Weinreb, S. M. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 401-444.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 401-444
    • Weinreb, S.M.1
  • 14
    • 0001197388 scopus 로고
    • Sulfones 14 were prepared in two steps starting from styryl oxide; see
    • Sulfones 14 were prepared in two steps starting from styryl oxide; see: Vougioukas, A. E.; Kagan, H. B. Tetrahedron Lett. 1987, 28, 6065-6068
    • (1987) Tetrahedron Lett. , vol.28 , pp. 6065-6068
    • Vougioukas, A.E.1    Kagan, H.B.2
  • 17
    • 84872212160 scopus 로고    scopus 로고
    • +-specific chelating agent, see, e.g. ref 2 or
    • +-specific chelating agent, see, e.g., ref 2 or Tamao, K.; Nakagawa, Y.; Ito, Y. Org. Synth. 1996, 73, 1035-1042
    • (1996) Org. Synth. , vol.73 , pp. 1035-1042
    • Tamao, K.1    Nakagawa, Y.2    Ito, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.