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Volumn 46, Issue 32, 2005, Pages 5265-5268

Erratum: Fragmentation of carbohydrate anomeric alkoxyl radicals. Synthesis of highly functionalized chiral vinyl sulfones (Tetrahedron Letters (2005) 46 (5265) DOI: 10.1016/j.tetlet.2005.06.043);Fragmentation of carbohydrate anomeric alkoxyl radicals. Synthesis of highly functionalized chiral vinyl sulfones

Author keywords

Alkoxyl radical; Carbohydrate; Radical reaction; Vinyl sulfone

Indexed keywords

BENZENE; CARBOHYDRATE DERIVATIVE; IODINE; MERCURY DERIVATIVE; VINYL DERIVATIVE;

EID: 21844462579     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.12.035     Document Type: Erratum
Times cited : (19)

References (47)
  • 9
  • 35
  • 45
    • 0030492285 scopus 로고    scopus 로고
    • The tri-O-acetyl-d-glucal (7 ), precursor of sulfones 12 and 13, is commercially available. Tri-O-acetyl-l-rhamnal (9 ), tri-O-acetyl-d-galactal (10 ), and tri-O-acetyl-d-lactal (11 ) were easily prepared according to: B.K. Shull, Z. Wu, and M. Koreeda J. Carbohydr. Chem. 15 1996 955 964
    • (1996) J. Carbohydr. Chem. , vol.15 , pp. 955-964
    • Shull, B.K.1    Wu, Z.2    Koreeda, M.3
  • 46
    • 21844439698 scopus 로고    scopus 로고
    • note
    • 4, concentrated under vacuum, and the residue used in the next reaction without purification.
  • 47
    • 21844459163 scopus 로고    scopus 로고
    • note
    • 2. The organic layer was washed with 10% aqueous sodium thiosulfate, dried, and concentrated in vacuo. Chromatotron chromatography of the residue (hexanes-EtOAc mixtures) afforded the required vinyl sulfones.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.