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Volumn 51, Issue 6, 2010, Pages 895-898

Conversion of l-rhamnose into ten of the sixteen 1- and 6-deoxyketohexoses in water with three reagents: d-tagatose-3-epimerase equilibrates C3 epimers of deoxyketoses

Author keywords

[No Author keywords available]

Indexed keywords

1 DEOXYFRUCTOSE; 1 DEOXYKETOHEXOSE; 1 DEOXYPSICOSE; 1 DEOXYTAGATOSE; 6 DEOXYFRUCTOSE; 6 DEOXYKETOHEXOSE; 6 DEOXYPSICOSE; 6 DEOXYTAGATOSE; KETOSE; REAGENT; RHAMNOSE; TAGATOSE; TAGATOSE 3 EPIMERASE; UNCLASSIFIED DRUG;

EID: 73249136791     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.12.024     Document Type: Article
Times cited : (30)

References (44)
  • 17
    • 73249137058 scopus 로고    scopus 로고
    • note
    • Whereas d-erythrose has R configuration at C3 and S at C2, any higher alditol related to d-erythritol will have R configuration at both carbons adjacent to the terminal C; this stereochemical motif is referred to in the Letter as t-RR [t for terminal C]. Alditols similarly related to d-threitol are described as t-RS, whereas l-erythritol is t-SS and l-threitol is t-SR.
  • 42
    • 73249120971 scopus 로고    scopus 로고
    • note
    • B).
  • 44
    • 73249142435 scopus 로고    scopus 로고
    • note
    • 13C NMR spectra of all the deoxyketoses prepared in this Letter.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.