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Volumn 12, Issue 19, 2010, Pages 4352-4355

Organocatalytic asymmetric synthesis of chiral pyrrolizines by cascade conjugate addition-aldol reactions

Author keywords

[No Author keywords available]

Indexed keywords

3-HYDROXYBUTANAL; ALDEHYDE; ALDOL; PYRROLE DERIVATIVE;

EID: 77957164101     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101811c     Document Type: Article
Times cited : (48)

References (61)
  • 4
    • 77957137943 scopus 로고    scopus 로고
    • For examples of enantioselective organocatalyses using N -centered heteroaromatic nucleophiles, see
    • For examples of enantioselective organocatalyses using N -centered heteroaromatic nucleophiles, see
  • 7
    • 77957145469 scopus 로고    scopus 로고
    • For examples of enantioselective transition-metal catalyses using N -centered heteroaromatic nucleophiles, see
    • For examples of enantioselective transition-metal catalyses using N -centered heteroaromatic nucleophiles, see
  • 10
    • 77957116637 scopus 로고    scopus 로고
    • For recent reviews of organocatalytic asymmetric cascade reactions, see
    • For recent reviews of organocatalytic asymmetric cascade reactions, see
  • 15
    • 77957153332 scopus 로고    scopus 로고
    • For synthesis of chiral heterocycles via organocatalytic cascade Michael-aldol reactions, see
    • For synthesis of chiral heterocycles via organocatalytic cascade Michael-aldol reactions, see
  • 20
    • 77957151805 scopus 로고    scopus 로고
    • For examples of pyrroles as C -centered nucleophiles for enantioselective organocatalyses, see the following
    • For examples of pyrroles as C -centered nucleophiles for enantioselective organocatalyses, see the following.
  • 24
    • 0034807741 scopus 로고    scopus 로고
    • Friedel-Crafts alkylation with α,β-unsaturated aldehydes
    • Friedel-Crafts alkylation with α,β-unsaturated aldehydes: Paras, N. A.; MacMillan, D. W. C. J. Am. Chem. Soc. 2001, 123, 4370
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 4370
    • Paras, N.A.1    MacMillan, D.W.C.2
  • 41
    • 77957144135 scopus 로고    scopus 로고
    • For recent reviews of organocatalytic asymmetric conjugate addition reactions, see
    • For recent reviews of organocatalytic asymmetric conjugate addition reactions, see
  • 45
    • 77957146194 scopus 로고    scopus 로고
    • For the first development of diarylprolinol silyl ethers as organocatalysts, see
    • For the first development of diarylprolinol silyl ethers as organocatalysts, see
  • 49
    • 77957105779 scopus 로고    scopus 로고
    • note
    • 2H was the best reagent.
  • 50
    • 77957160859 scopus 로고    scopus 로고
    • For general reviews in this area, see
    • For general reviews in this area, see
  • 55
    • 77957154506 scopus 로고    scopus 로고
    • Under the optimized reaction conditions, the cascade reaction did not proceed with pyrroles bearing less electrophilic carbonyl substituent such as 2-acetylpyrrole and 2-acetyl-4-cyanopyrrole
    • Under the optimized reaction conditions, the cascade reaction did not proceed with pyrroles bearing less electrophilic carbonyl substituent such as 2-acetylpyrrole and 2-acetyl-4-cyanopyrrole.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.