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Volumn 12, Issue 15, 2010, Pages 3556-3559

Stereoselective synthesis of 1,2,3,4-tetrasubstituted dienes from allenoates and aldehydes: An observation of phosphine-induced chemoselectivity

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKADIENE; PHOSPHINE; PHOSPHINE DERIVATIVE;

EID: 77955156821     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101429z     Document Type: Article
Times cited : (47)

References (67)
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    • Normant, J. F. Modern Synthetic Methods; Scheffold, R., Ed.; Wiley: Chichester, 1983; Vol. 3, pp 139-171.
    • (1983) Modern Synthetic Methods , vol.3 , pp. 139-171
    • Normant, J.F.1
  • 14
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    • For leading reviews, see: (a) Ref 2c
    • For leading reviews, see: (a) Ref 2c.
  • 20
    • 77955130721 scopus 로고    scopus 로고
    • Ref 2c
    • Ref 2c.
  • 31
    • 77955134782 scopus 로고    scopus 로고
    • For recent reviews, see
    • For recent reviews, see
  • 35
    • 22944485617 scopus 로고    scopus 로고
    • Ma, S. Chem. Rev. 2005, 105, 2829
    • (2005) Chem. Rev. , vol.105 , pp. 2829
    • Ma, S.1
  • 39
    • 77955140667 scopus 로고    scopus 로고
    • For selected examples, see
    • For selected examples, see
  • 52
    • 77955157446 scopus 로고    scopus 로고
    • An air-stable and water-soluble phosphine, often used as a nucleophilic trialkylphosphine. See ref 10 and references cited therein
    • An air-stable and water-soluble phosphine, often used as a nucleophilic trialkylphosphine. See ref 10 and references cited therein.
  • 53
    • 77955155463 scopus 로고    scopus 로고
    • The exceptional reactivity of o-substituted benzaldehydes, which presumably results from the increased steric hindrance, in the reactions with allenoates was also observed in ref 12a
    • The exceptional reactivity of o-substituted benzaldehydes, which presumably results from the increased steric hindrance, in the reactions with allenoates was also observed in ref 12a.
  • 54
    • 77955164875 scopus 로고    scopus 로고
    • A distinct Wittig olefination of α-methyl allenoate 1f with salicylaldehydes or aromatic aldehydes to form trisubstituted dienes was observed
    • A distinct Wittig olefination of α-methyl allenoate 1f with salicylaldehydes or aromatic aldehydes to form trisubstituted dienes was observed
  • 58
    • 77955153405 scopus 로고    scopus 로고
    • For representative studies on the water-assisted hydrogen shift in nucleophilic phosphine catalyses of allenoates, see: (a) refs 9c and 9d
    • For representative studies on the water-assisted hydrogen shift in nucleophilic phosphine catalyses of allenoates, see: (a) refs 9c and 9d.
  • 65
    • 77955136494 scopus 로고    scopus 로고
    • For representative examples, see: (a) Refs 10 and 20b
    • For representative examples, see: (a) Refs 10 and 20b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.