메뉴 건너뛰기




Volumn 70, Issue 16, 2005, Pages 6474-6483

Stereocontrolled synthesis of a complex library via elaboration of angular epoxyquinol scaffolds

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; AMINES; CARBONYLATION; DEHYDRATION; HYDROGENATION; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 23044481109     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050956y     Document Type: Article
Times cited : (39)

References (101)
  • 27
    • 33544465171 scopus 로고    scopus 로고
    • PCT Int. Appl. 1996, WO 9603424
    • For select examples, see: (a) Boger, D. L. PCT Int. Appl. 1996, WO 9603424.
    • Boger, D.L.1
  • 45
    • 33544467869 scopus 로고    scopus 로고
    • note
    • See the Supporting Information for further details.
  • 67
    • 0001658980 scopus 로고
    • (b) For a review of stereoelectronic control in the reactions of ketones and their enolates, see: Pollack, R. M. Tetrahedron 1989, 45, 4913.
    • (1989) Tetrahedron , vol.45 , pp. 4913
    • Pollack, R.M.1
  • 79
    • 33544472905 scopus 로고    scopus 로고
    • note
    • For details on the syntheses of dienophiles M5 and T4, see the Supporting Information.
  • 80
    • 1642271318 scopus 로고    scopus 로고
    • For the synthesis and application of dienophile scavenger resin 37, see: Lei, X.; Porco, J. A., Jr. Org. Lett. 2004, 6, 795.
    • (2004) Org. Lett. , vol.6 , pp. 795
    • Lei, X.1    Porco Jr., J.A.2
  • 81
    • 0035935115 scopus 로고    scopus 로고
    • (a) B1, B2, B6, B7, and B8 are commercially available. (b) For the syntheses of B3, B4, and B5, see: Supporting Information. (c) For synthesis of B9, see: Renaudet, O.; Dumy, P. Tetrahedron Lett. 2001, 42, 7575.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 7575
    • Renaudet, O.1    Dumy, P.2
  • 83
    • 33544473967 scopus 로고    scopus 로고
    • note
    • HPLC purity values refer to the sum of the HPLC (ELSD) area % for oxime E/Z isomers.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.