메뉴 건너뛰기




Volumn 131, Issue 6, 2009, Pages 2086-2087

Enantioselective intramolecular friedel-crafts-type α-arylation of aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLATION; ARYLATION; CYTOTOXIC AGENTS; ELECTRON-DONATING GROUP; ENANTIOSELECTIVE; FRIEDEL-CRAFTS; HUMAN ADENOCARCINOMA; TOTAL SYNTHESIS; VINYLATION;

EID: 67749114483     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja809405c     Document Type: Article
Times cited : (155)

References (20)
  • 8
    • 0034654216 scopus 로고    scopus 로고
    • For examples of proline-based catalysis involving enamines, see: (a) List, B, Lerner, R. A, Barbas, C. F, III. J. Am. Chem. Soc. 2000, 122, 2395
    • For examples of proline-based catalysis involving enamines, see: (a) List, B.; Lerner, R. A.; Barbas, C. F., III. J. Am. Chem. Soc. 2000, 122, 2395.
  • 10
    • 33744826542 scopus 로고    scopus 로고
    • For examples of prolinol-derived ligands for enamine catalysis, see: (a) Chi, Y, Gellman, S. H. J. Am. Chem. Soc. 2006, 128, 6804
    • For examples of prolinol-derived ligands for enamine catalysis, see: (a) Chi, Y.; Gellman, S. H. J. Am. Chem. Soc. 2006, 128, 6804.
  • 14
    • 84891744494 scopus 로고    scopus 로고
    • See the Supporting Information for the preparation of 1c. CCDC 709588 contains the supplementary crystallographic data for 1c and is available free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ data-request/cif.
    • See the Supporting Information for the preparation of 1c. CCDC 709588 contains the supplementary crystallographic data for 1c and is available free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ data-request/cif.
  • 15
    • 84891747225 scopus 로고    scopus 로고
    • In view of the requirement of electron donating substituents on the aromatic nucleus for this reaction, we favored the cationic rather than the radical mechanism operating in the corresponding reactions with alkenes see refs 1 and 2
    • In view of the requirement of electron donating substituents on the aromatic nucleus for this reaction, we favored the cationic rather than the radical mechanism operating in the corresponding reactions with alkenes (see refs 1 and 2).
  • 16
    • 0006043219 scopus 로고
    • For the previous enantioselective total syntheses, see: a
    • For the previous enantioselective total syntheses, see: (a) Tietze, L. F.; Raschke, T. Synlett 1995, 6, 597.
    • (1995) Synlett , vol.6 , pp. 597
    • Tietze, L.F.1    Raschke, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.