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Volumn 70, Issue 20, 2005, Pages 8027-8034

Stereoselective syntheses of highly functionalized bicyclo[3.1.0]hexanes: A general methodology for the synthesis of potent and selective mGluR2/3 agonists

Author keywords

[No Author keywords available]

Indexed keywords

REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 25444486184     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0511187     Document Type: Article
Times cited : (23)

References (38)
  • 10
    • 0038141859 scopus 로고    scopus 로고
    • Holden, C. Science 2003, 300, 1866.
    • (2003) Science , vol.300 , pp. 1866
    • Holden, C.1
  • 23
    • 0035959461 scopus 로고    scopus 로고
    • (a) An intramolecular cyclopropanation reaction of ester enolate to an iodide has been reported and complete F-endo products were observed. See: Saito, A.; Ito, H.; Taguchi, T. Tetrahedron 2001, 57, 7487.
    • (2001) Tetrahedron , vol.57 , pp. 7487
    • Saito, A.1    Ito, H.2    Taguchi, T.3
  • 34
    • 25444492513 scopus 로고    scopus 로고
    • note
    • 6 at room temperature and was decomposed completely to a mixture of several aromatic compounds in 3-5 days.
  • 35
    • 25444531850 scopus 로고    scopus 로고
    • note
    • In ref 5e, the desired hydantoin was obtained in 16% yield from the ethyl ester of the enantiomer of hydroxy ketone 17 under Bucherer-Bergs conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.