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Volumn 4, Issue 6, 2014, Pages 2772-2775

Stereoselective synthesis of conjugated α-Z/γ-E and α-Z/γ-Z dienoic acids. Kinetic torquoselectivity versus thermodynamic control

Author keywords

[No Author keywords available]

Indexed keywords

GRIGNARD REAGENT; STEREOCONTROL; STEREOSELECTIVE ADDITION; STEREOSELECTIVE SYNTHESIS; THERMODYNAMIC CONTROL; TORQUOSELECTIVITY;

EID: 84890726239     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c3ra45309j     Document Type: Article
Times cited : (12)

References (46)
  • 38
    • 0001327661 scopus 로고
    • 8. This result suggests that the 6-π electrocyclic ring opening reaction operates on the cyclic enolate and not on the cyclic enolsilyl ether. This suggests that in the mechanism TMSCl activates the methoxycarbonyl instead of the lactone
    • R. Gompper O. Christmann Chem. Ber. 1961 94 1795
    • (1961) Chem. Ber. , vol.94 , pp. 1795
    • Gompper, R.1    Christmann, O.2
  • 43
    • 0026568881 scopus 로고
    • For more theoretical studies on thermally disrotatory 6-π electrocyclic processes see
    • Y. Zhu S. Ganapathy R. S. H. Liu J. Org. Chem. 1992 57 1110
    • (1992) J. Org. Chem. , vol.57 , pp. 1110
    • Zhu, Y.1    Ganapathy, S.2    Liu, R.S.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.