메뉴 건너뛰기




Volumn 9, Issue 18, 2007, Pages 3667-3670

Stereoselective conjugate addition of aryl- And alkenylboronic acids to acyclic γ,δ-oxygen-substituted α,β-enoates

Author keywords

[No Author keywords available]

Indexed keywords


EID: 34548543339     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7016033     Document Type: Article
Times cited : (19)

References (31)
  • 1
    • 5244346814 scopus 로고    scopus 로고
    • First report: Sakai, M.; Hayashi, H.; Miyaura, N. Organometallics 1997, 16, 4229.
    • First report: Sakai, M.; Hayashi, H.; Miyaura, N. Organometallics 1997, 16, 4229.
  • 2
    • 0034975355 scopus 로고    scopus 로고
    • Reviews: a
    • Reviews: (a) Hayashi, T. Synlett 2001, 879.
    • (2001) Synlett , pp. 879
    • Hayashi, T.1
  • 8
    • 0041528503 scopus 로고    scopus 로고
    • For recent leading references on the synthesis of boronic acids and derivatives, see: a
    • For recent leading references on the synthesis of boronic acids and derivatives, see: (a) Kalinin, A. V.; Scherer, S.; Snieckus, V. Angew. Chem., Int. Ed. 2003, 42, 3399.
    • (2003) Angew. Chem., Int. Ed , vol.42 , pp. 3399
    • Kalinin, A.V.1    Scherer, S.2    Snieckus, V.3
  • 15
    • 17844373774 scopus 로고    scopus 로고
    • 1 reagents to γ-OH-substituted cyclic enones, see: de la Herrán, G.; Mba, M.; Murcia, M. C.; Plumet, J.; Csáky, A. G. Org. Lett. 2005, 7, 1669.
    • 1 reagents to γ-OH-substituted cyclic enones, see: de la Herrán, G.; Mba, M.; Murcia, M. C.; Plumet, J.; Csáky, A. G. Org. Lett. 2005, 7, 1669.
  • 22
    • 0037764896 scopus 로고    scopus 로고
    • For other OH-free directed conjugate additions of RMgX and RLi reagents to open-chain systems, see: a
    • For other OH-free directed conjugate additions of RMgX and RLi reagents to open-chain systems, see: (a) Fleming, F. F.; Wang, Q.; Steward, O. W. J. Org. Chem. 2003, 68, 4235.
    • (2003) J. Org. Chem , vol.68 , pp. 4235
    • Fleming, F.F.1    Wang, Q.2    Steward, O.W.3
  • 29
    • 34548527919 scopus 로고    scopus 로고
    • This is to be compared with the additions of vinyl-Rh1 species to γ-OH-substituted cyclic enones, which may take place under chelation or nonchelation control, and similar additions of Ar-Rh1 species, which take place under nonchelation control. See ref 6
    • 1 species, which take place under nonchelation control. See ref 6.
  • 30
    • 0000458209 scopus 로고
    • For OH-directed stereoselectivity in Rh-catalyzed hydrogenation reactions, see:, and references cited therein
    • For OH-directed stereoselectivity in Rh-catalyzed hydrogenation reactions, see: Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307 and references cited therein.
    • (1993) Chem. Rev , vol.93 , pp. 1307
    • Hoveyda, A.H.1    Evans, D.A.2    Fu, G.C.3
  • 31
    • 33645523429 scopus 로고    scopus 로고
    • Similar models have been used to interpret the addition reactions of other nucleophiles to γ-hydroxy-substituted α,β-unsaturated esters. See: Kireev, A. S, Manpadi, M, Kornienko, A. J. Org. Chem. 2006, 71, 2630 and references cited therein
    • Similar models have been used to interpret the addition reactions of other nucleophiles to γ-hydroxy-substituted α,β-unsaturated esters. See: Kireev, A. S.; Manpadi, M.; Kornienko, A. J. Org. Chem. 2006, 71, 2630 and references cited therein.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.