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Volumn , Issue 5, 2005, Pages 793-796

Chiral auxiliaries as docking/protecting groups in biohydroxylation: (S)-specific hydroxylation of enantiopure tert-butyl-substituted spirooxazolidines derived from cyclopentanone

Author keywords

Biohydroxylation; Biotransformations; Enantioselectivity; Substrate engineering

Indexed keywords

CARBON; CYCLOPENTANONE DERIVATIVE; HYDROXYL GROUP; OXAZOLIDINE DERIVATIVE; PENTANE; SPIROOXAZOLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 15044348499     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400636     Document Type: Article
Times cited : (8)

References (11)
  • 3
    • 33748228947 scopus 로고    scopus 로고
    • G. Asensio, R. Mello, M. E. González-Núnez, G. Castellano, J. Corral, Angew. Chem. 1996, 108, 196-198; Angew. Chem. Int. Ed. 1996, 35, 217-218.
    • (1996) Angew. Chem. Int. Ed. , vol.35 , pp. 217-218
  • 9
    • 15044363008 scopus 로고    scopus 로고
    • note
    • A number of reaction variables, such as reaction temperature, reaction solvent and order of reagent addition, were examined in an effort to improve the yields of compounds 7 and 8.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.