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Volumn 78, Issue 22, 2013, Pages 11483-11493

Tandem Blaise/retro-Blaise reaction for the nitrile-mediated regioselective intermolecular addition of unstabilized zinc ester enolates (Reformatsky Reagents) to 1-alkynes and 1,3-enynes

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION PRODUCTS; DIELS-ALDER REACTION; ESTER ENOLATES; INTERMOLECULAR ADDITIONS; OXIDATIVE AROMATIZATION; REFORMATSKY REAGENTS; REGIO-SELECTIVE; REVERSIBLE ADDITION;

EID: 84887945979     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo402015n     Document Type: Article
Times cited : (18)

References (66)
  • 2
    • 34548428596 scopus 로고    scopus 로고
    • In; Rappoport, Z. Marek, I. Wiley: Chichester, U.K. Chapter 19
    • Lothiois, E.; Meyer, C. In The Chemistry of Organozinc Compounds; Rappoport, Z., Marek, I., Eds.; Wiley: Chichester, U.K., 2006; Chapter 19, p 863.
    • (2006) The Chemistry of Organozinc Compounds , pp. 863
    • Lothiois, E.1    Meyer, C.2
  • 56
    • 68949163947 scopus 로고    scopus 로고
    • Chang and co-workers reported that a nitrile can be used as an accelerator in Rh-catalyzed conversion of aldoximes to amides, see
    • Chang and co-workers reported that a nitrile can be used as an accelerator in Rh-catalyzed conversion of aldoximes to amides, see: Kim, M.; Lee, J.; Lee, H.-Y.; Chang, S. Adv. Synth. Catal. 2009, 351, 1807
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 1807
    • Kim, M.1    Lee, J.2    Lee, H.-Y.3    Chang, S.4
  • 57
    • 84865467710 scopus 로고    scopus 로고
    • trans can be synthesized by direct reaction of a Reformatsky reagent 1a with acetophenone in the presence of stoichiometric amount of diphenylphosphite in a 45% yield. See
    • trans-5a can be synthesized by direct reaction of a Reformatsky reagent 1a with acetophenone in the presence of stoichiometric amount of diphenylphosphite in a 45% yield. See: Cui, H.; Li, Y.; Zhang, S. Org. Biomol Chem. 2012, 10, 2862
    • (2012) Org. Biomol Chem. , vol.10
    • Cui, H.1    Li, Y.2    Zhang, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.