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Volumn 70, Issue 6, 2005, Pages 2409-2412

Enantioselective approaches to potential MetAP-2 reversible inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; STEREOCHEMISTRY; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 15444377540     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo047858h     Document Type: Article
Times cited : (30)

References (28)
  • 22
    • 0037266148 scopus 로고    scopus 로고
    • Compound 17 was prepared in a few steps from the known 4-(4-methoxy-benzyloxy)-cyclohexanone (Spino, C.; Hill, B.; Dube, P.; Gingras, S. Can. J. Chem. 2003, 81, 81-108); the ketone was converted to the corresponding enol triflate and the latter was converted to 17 as described in the preparation of 14 (see Supporting Information for details).
    • (2003) Can. J. Chem. , vol.81 , pp. 81-108
    • Spino, C.1    Hill, B.2    Dube, P.3    Gingras, S.4
  • 23
    • 15444369188 scopus 로고    scopus 로고
    • note
    • At the time this work was in progress, the enantioselective synthesis of the required Sorensen's intermediate had not been disclosed (ref 14a).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.