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Volumn 354, Issue 2-3, 2012, Pages 364-370

Enantioselective conjugate addition of nitroalkanes to alkylidenemalonates promoted by thiourea-based bifunctional organocatalysts

Author keywords

alkylidenemalonates; asymmetric organocatalysis; bifunctional thioureas; Michael reaction; nitro compounds

Indexed keywords


EID: 84857288724     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201100732     Document Type: Article
Times cited : (24)

References (60)
  • 6
    • 6044269452 scopus 로고    scopus 로고
    • See also
    • Angew. Chem. Int. Ed. 2004, 43, 5138-5175. See also
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5138-5175
  • 23
    • 78649855595 scopus 로고    scopus 로고
    • γ-Nitro carbonyl compounds are also achievable by the organocatalysed addition of aldehydes to nitroalkenes. For examples, see
    • D. Roca-Lopez, D. Sadaba, I. Delso, R. P. Herrera, T. Tejero, P. Merino, Tetrahedron: Asymmetry 2010, 21, 2561-2601. γ-Nitro carbonyl compounds are also achievable by the organocatalysed addition of aldehydes to nitroalkenes. For examples, see
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 2561-2601
    • Roca-Lopez, D.1    Sadaba, D.2    Delso, I.3    Herrera, R.P.4    Tejero, T.5    Merino, P.6
  • 25
    • 22144459070 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4212-4215
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4212-4215
  • 36
    • 21244471124 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4032-4035
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4032-4035


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.