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Volumn 11, Issue 1, 2000, Pages 305-317

Stereoselective synthesis of C-glycosylphosphonates from their ketols. Reconsideration of an abandoned route

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSYL 1 PHOSPHATE; METHYLPHOSPHONIC ACID; PHOSPHONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034000692     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00477-2     Document Type: Article
Times cited : (35)

References (42)
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    • and references cited therein
    • For other types of aldose 1-phosphate analogues, such as non-isosteric but isopolar phosphonates, and ketosyl- and ulosonylphosphonates, see: Dondoni, A.; Daninos, S.; Marra, A.; Formaglio, P. Tetrahedron 1998, 54, 9859 and references cited therein.
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    • Ref. 3a, p. 71
    • Ref. 3a, p. 71.
  • 32
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    • note
    • The α-D anomeric configuration of ketopyranoses 2a-d and ketofuranose 10 was supported by a substantial NOE between HO-2 and H-6 or H-5, respectively. Furthermore, HO-2 of ketoses 2a-c showed a long range (W) coupling with H-3.
  • 33
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    • note
    • The geometric configuration of the exocyclic enol ethers 4a, 4d, and 12 was assigned by NOE experiments.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.