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Volumn 64, Issue 14, 1999, Pages 5224-5229

On the role of neighboring group participation and ortho esters in β- xylosylation: 13C NMR observation of a bridging 2-phenyl-1,3-dioxalenium ion

Author keywords

[No Author keywords available]

Indexed keywords

2 PHENYL 1,3 DIOXALENIUM; CARBON 13; ESTER; ION; PYRANOSIDE; SULFOXIDE; THIOGLYCOSIDE; UNCLASSIFIED DRUG;

EID: 0032996670     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990424f     Document Type: Article
Times cited : (97)

References (36)
  • 9
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    • Ph.D. Thesis, Princeton
    • Walker, S. Ph.D. Thesis, Princeton, 1992.
    • (1992)
    • Walker, S.1
  • 10
    • 0345709764 scopus 로고    scopus 로고
    • Senior Thesis, Princeton
    • Laurich, V. M. Senior Thesis, Princeton, 1997.
    • (1997)
    • Laurich, V.M.1
  • 11
    • 0345709763 scopus 로고    scopus 로고
    • Ph.D. Thesis, Princeton
    • Van, L. Ph.D. Thesis, Princeton, 1996.
    • (1996)
    • Van, L.1
  • 27
    • 0345709758 scopus 로고    scopus 로고
    • note
    • We suspect that the α/β mixture of xylosides obtained in this experiment is a function of scrambling of anomeric stereochemistry under the strongly acidic conditions rather than of any lack of selectivity in the initial glycoside-forming reaction.
  • 36
    • 0344415138 scopus 로고    scopus 로고
    • note
    • 13C in the carbonyl carbon was obtained from Cambridge Isotope Laboratories, Woburn, MA 01801.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.