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Volumn , Issue 19, 2010, Pages 2827-2838

Proline sulfonamide based organocatalysis: Better late than never

Author keywords

aldol reaction; amino acids; asymmetric catalysis; enantioselectivity; Michael addition; multicomponent reaction; phase transfer catalysis; solvent effects; sulfonamides

Indexed keywords

PROLINE SULFONAMIDE; SOLVENT; SULFONAMIDE; UNCLASSIFIED DRUG;

EID: 78650173761     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1259020     Document Type: Review
Times cited : (65)

References (134)
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    • Sigma-Aldrich Catalog Numbers: 733008 (S)-isomer 733016 (R)-isomer. Synthetech Inc. Catalog Numbers: 24C806 (S)-isomer 24C805 (R)-isomer.
    • Sigma-Aldrich Catalog Numbers: 733008 (S)-isomer 733016 (R)-isomer. Synthetech Inc. Catalog Numbers:24C806 (S)-isomer 24C805 (R)-isomer.
  • 73
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    • Meciarova and Toma have explored the use of ionic liquids as alternative solvent systems for proline sulfonamide catalyzed aldol reactions, Mannich reactions, and Michael additions
    • Meciarova and Toma have explored the use of ionic liquids as alternative solvent systems for proline sulfonamide catalyzed aldol reactions, Mannich reactions, and Michael additions:, Meciarová M, Toma S, Berkessel A, Koch B, Lett. Org. Chem. 2006 3 437
    • (2006) Lett. Org. Chem. , vol.3 , pp. 437
    • Meciarová, M.1    Toma, S.2    Berkessel, A.3    Koch, B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.