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Volumn 68, Issue 17, 2003, Pages 6839-6841

Conversion of (-)-3-dehydroshikimic acid into derivatives of the (+)-enantiomer

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOMERS;

EID: 0042890560     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo034689c     Document Type: Article
Times cited : (13)

References (20)
  • 3
    • 0041903624 scopus 로고    scopus 로고
    • Draths, K. M., Kambourakis, S., Li, K., Frost, J. W., Eds.; ACS Symposium Series 784; American Chemical Society: Washington, DC
    • Chemicals and Materials from Renewable Resources; Draths, K. M., Kambourakis, S., Li, K., Frost, J. W., Eds.; ACS Symposium Series 784; American Chemical Society: Washington, DC, 2001; p 133.
    • (2001) Chemicals and Materials from Renewable Resources , pp. 133
  • 14
    • 0027325480 scopus 로고
    • 2O resulted in a ca. 2:1 mixture of bis-acetal 9 and its regioisomer (77% combined yield). The use of chiral bis-DHP derivatives (see, for example: Boons, G.-J.; Entwistle, D. A.; Ley, S. V.; Woods, M. Tetrahedron Lett. 1993, 34, 5649) to effect more selective conversion of compound 5 into target 11 was not considered because of the likely high cost of producing such protecting agents and the multistep syntheses necessary for their preparation.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 5649
    • Boons, G.-J.1    Entwistle, D.A.2    Ley, S.V.3    Woods, M.4
  • 15
    • 12444332295 scopus 로고    scopus 로고
    • note
    • "Precipitated active" manganese dioxide as supplied by MERCK-Schuchardt was used.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.