메뉴 건너뛰기




Volumn 18, Issue 13, 2007, Pages 1533-1539

The intramolecular tandem Michael/Mannich-type reaction of α,β-unsaturated carbonyl compounds with acyliminium ions provides access to chiral indolizidines

Author keywords

[No Author keywords available]

Indexed keywords

ACYLIMINIUM DERIVATIVE; CARBONYL DERIVATIVE; IMINE; INDOLIZIDINE DERIVATIVE; OXAZOLIDINONE DERIVATIVE; SOLVENT; TITANIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34547141215     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.06.009     Document Type: Article
Times cited : (12)

References (53)
  • 18
    • 34547195628 scopus 로고    scopus 로고
    • Ref. 5.
  • 19
    • 34547232934 scopus 로고    scopus 로고
    • 2AlI mediated reactions, see Ref. 2a.
  • 24
    • 34547212185 scopus 로고    scopus 로고
    • Ref. 8.
  • 25
    • 0037126220 scopus 로고    scopus 로고
    • 2 mediated reactions, see
    • 2 mediated reactions, see. Wei H.-X., Kim S.H., and Li G. Org. Lett. 4 (2002) 3691
    • (2002) Org. Lett. , vol.4 , pp. 3691
    • Wei, H.-X.1    Kim, S.H.2    Li, G.3
  • 40
    • 34249688755 scopus 로고    scopus 로고
    • Very recently, an example of the aza-Baylis Hillman reaction via N-acyliminium ion has been reported, see
    • Very recently, an example of the aza-Baylis Hillman reaction via N-acyliminium ion has been reported, see. Myers E.L., De Vries J.G., and Aggarwal V.K. Angew. Chem., Int. Ed. 46 (2007) 1893
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 1893
    • Myers, E.L.1    De Vries, J.G.2    Aggarwal, V.K.3
  • 44
    • 34547149397 scopus 로고    scopus 로고
    • note
    • 4, Lewis acid/MeOH) gave the same result.
  • 48
    • 34247570300 scopus 로고
    • For examples of the conjugated addition of chloride to α,β-unsaturated chiral imides using Evans-type oxazolidinones, see
    • For examples of the conjugated addition of chloride to α,β-unsaturated chiral imides using Evans-type oxazolidinones, see. Cadillo G., De Simone A., Gentilucci L., and Tomasini C. J. Chem. Soc., Chem. Commun. (1994) 735
    • (1994) J. Chem. Soc., Chem. Commun. , pp. 735
    • Cadillo, G.1    De Simone, A.2    Gentilucci, L.3    Tomasini, C.4
  • 50
    • 34547159577 scopus 로고    scopus 로고
    • note
    • 5, 393.1217; found, 393.1096.
  • 51
    • 24944565287 scopus 로고    scopus 로고
    • {A figure is presented} Recently, an example of the tandem Michael-aldol reaction of chalcogenide-enones possessing a chiral oxazolidinethione for synthesis of 3-sulfanylpropanols containing three stereogenic centers has been reported, see
    • {A figure is presented} Recently, an example of the tandem Michael-aldol reaction of chalcogenide-enones possessing a chiral oxazolidinethione for synthesis of 3-sulfanylpropanols containing three stereogenic centers has been reported, see. Kinoshita H., Takahashi N., Iwamura T., Watanabe S., Kataoka T., Muraoka O., and Tanabe G. Tetrahedron Lett. 46 (2005) 7155
    • (2005) Tetrahedron Lett. , vol.46 , pp. 7155
    • Kinoshita, H.1    Takahashi, N.2    Iwamura, T.3    Watanabe, S.4    Kataoka, T.5    Muraoka, O.6    Tanabe, G.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.