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Volumn 13, Issue 5, 2011, Pages 1258-1260

Investigation of the stereochemistry of intermolecular conjugate additions of nucleophiles to acyclic nitrosoalkenes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKENE; NITROSO DERIVATIVE;

EID: 79952120574     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2000793     Document Type: Article
Times cited : (23)

References (38)
  • 1
    • 12344313515 scopus 로고
    • For reviews of vinylnitroso compounds and lead references see
    • For reviews of vinylnitroso compounds and lead references see: Gilchrist, T. L. Chem. Soc. Rev. 1983, 11, 53
    • (1983) Chem. Soc. Rev. , vol.11 , pp. 53
    • Gilchrist, T.L.1
  • 3
    • 0001675637 scopus 로고
    • For representative examples of enolonium ion equivalents see
    • For representative examples of enolonium ion equivalents see: Sacks, C. E.; Fuchs, P. L. J. Am. Chem. Soc. 1975, 97, 7372
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 7372
    • Sacks, C.E.1    Fuchs, P.L.2
  • 24
    • 79952161198 scopus 로고    scopus 로고
    • 2 led to a single anti diastereomer in 73% yield.
    • 2 led to a single anti diastereomer in 73% yield.
  • 25
    • 79952169549 scopus 로고    scopus 로고
    • In a control experiment, α-chloro-O -silyloxime 3 was found to be unreactive towards potassium diethyl malonate at room temperature in the absence of TBAF.
    • In a control experiment, α-chloro-O -silyloxime 3 was found to be unreactive towards potassium diethyl malonate at room temperature in the absence of TBAF.
  • 33
    • 33947435343 scopus 로고
    • Synthesized from the corresponding known α-chloroaldehyde
    • Synthesized from the corresponding known α-chloroaldehyde: Emling, B. L.; Vogt, R. R.; Hennion, G. F. J. Am. Chem. Soc. 1941, 63, 1624
    • (1941) J. Am. Chem. Soc. , vol.63 , pp. 1624
    • Emling, B.L.1    Vogt, R.R.2    Hennion, G.F.3
  • 34
    • 79952160203 scopus 로고    scopus 로고
    • Prepared from the corresponding commercially available aldehyde (see Supporting Information).
    • Prepared from the corresponding commercially available aldehyde (see Supporting Information).
  • 36
    • 68949092539 scopus 로고    scopus 로고
    • For synthesis of other compounds closely related to nitrile 21 see
    • For synthesis of other compounds closely related to nitrile 21 see: Tka, N.; Kraiem, J.; Kacem, Y.; Hajri, A.; Hassine, B. B. C. R. Chim. 2009, 12, 1066
    • (2009) C. R. Chim. , vol.12 , pp. 1066
    • Tka, N.1    Kraiem, J.2    Kacem, Y.3    Hajri, A.4    Hassine, B.B.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.