메뉴 건너뛰기




Volumn 129, Issue 44, 2007, Pages 13360-13361

Reaction pathway of conjugate addition of lithium organozincates to s-trans-enones

Author keywords

[No Author keywords available]

Indexed keywords

ENONE DERIVATIVE; KETONE DERIVATIVE; LITHIUM DERIVATIVE; ORGANIC COMPOUND; UNCLASSIFIED DRUG; ZINC DERIVATIVE;

EID: 35948973877     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja070123k     Document Type: Article
Times cited : (21)

References (27)
  • 6
    • 0002563073 scopus 로고
    • Reviews: a
    • Reviews: (a) Posner, G. H. Org. React. 1972, 19, 1-113.
    • (1972) Org. React , vol.19 , pp. 1-113
    • Posner, G.H.1
  • 7
    • 0003417469 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon: Oxford University Press: UK
    • (b) Kozlowski, J. A. Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford University Press: UK, 1994.
    • (1994) Comprehensive Organic Synthesis
    • Kozlowski, J.A.1
  • 8
    • 35948968049 scopus 로고    scopus 로고
    • Book: Ho, T.-L. Hard and Soft Acids and Bases Principle in Organic Chemistry; Academic Press: New York, 1977.
    • Book: Ho, T.-L. Hard and Soft Acids and Bases Principle in Organic Chemistry; Academic Press: New York, 1977.
  • 12
    • 0034694687 scopus 로고    scopus 로고
    • 2 as chemical models for alkyllithium dimers and zincates, respectively. For details of theoretical methods and chemical models, see: (a) Hseffner, F. E.; Sun, C.; Williard, P. G. J. Am. Chem. Soc. 2000, 122, 12542-12546.
    • 2 as chemical models for alkyllithium dimers and zincates, respectively. For details of theoretical methods and chemical models, see: (a) Hseffner, F. E.; Sun, C.; Williard, P. G. J. Am. Chem. Soc. 2000, 122, 12542-12546.
  • 18
    • 35948955986 scopus 로고    scopus 로고
    • The additional single-point calculations with larger basis set confirm and validate the preference for 1,4- over 1,2-addition see Supporting Information, Table S1, for details
    • The additional single-point calculations with larger basis set confirm and validate the preference for 1,4- over 1,2-addition (see Supporting Information, Table S1, for details).
  • 19
    • 35948958238 scopus 로고    scopus 로고
    • NBO analysis was performed using 3CBOND and CHOOSE keywords in order to standardize the resonance structure representations of each TS. The descriptions are given in detail in the Supporting Information.
    • NBO analysis was performed using 3CBOND and CHOOSE keywords in order to standardize the resonance structure representations of each TS. The descriptions are given in detail in the Supporting Information.
  • 20
    • 11844291952 scopus 로고    scopus 로고
    • In the reaction of nucleophilic organometallics with α,α- unsaturated imines, 1,4-addition takes place much more easily than in the reaction with α,β-unsaturated carbonyl compounds, a Soeta, T, Kuriyama, M, Tomioka, K. J. Org. Chem. 2005, 70, 297-300
    • In the reaction of nucleophilic organometallics with α,α- unsaturated imines, 1,4-addition takes place much more easily than in the reaction with α,β-unsaturated carbonyl compounds, (a) Soeta, T.; Kuriyama, M.; Tomioka, K. J. Org. Chem. 2005, 70, 297-300.
  • 24
    • 35948963322 scopus 로고    scopus 로고
    • 2.
    • 2.
  • 25
    • 0037427234 scopus 로고    scopus 로고
    • Recently, Collum and co-workers reported that open form TS could be generated intentionally by utilizing bulky, poorly coordinating ethereal solvents in organolithium (homobimetal) chemistry, (a) Zhao, P.; Collum, D. B. J. Am. Chem. Soc. 2003, 125, 4008-4009.
    • Recently, Collum and co-workers reported that open form TS could be generated intentionally by utilizing bulky, poorly coordinating ethereal solvents in organolithium (homobimetal) chemistry, (a) Zhao, P.; Collum, D. B. J. Am. Chem. Soc. 2003, 125, 4008-4009.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.