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Volumn 2, Issue 24, 2000, Pages 3941-3943

Effecient, Diastereoselective Chemical Synthesis of a β-Mannopyranosyl Phosphoisoprenoid

Author keywords

[No Author keywords available]

Indexed keywords

ISOPRENOID PHOSPHATE SUGAR;

EID: 0034736360     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol006725p     Document Type: Article
Times cited : (22)

References (16)
  • 9
    • 0026580117 scopus 로고
    • The β-selective (4/1) phosphorylation of 2,3,4,6-tetra-O-acetylmannopyranose with limiting diphenyl chlorophosphidate has been reported: Sabesan, S.; Neira, S. Carbohydr. Res. 1992, 223, 169-185. It is highly unlikely that this method can be extended to the significantly less reactive dialkyl chlorophosphidates required for the synthesis of the present targets. Other groups typically report α-selective phosphorylation of mannose in this type of process even with diphenyl chlorophosphidate, e.g., Boger, D. L.; Teramoto, S.; Zhou, J. J. Am. Chem. Soc. 1995, 117, 7344- 7356.
    • (1992) Carbohydr. Res. , vol.223 , pp. 169-185
    • Sabesan, S.1    Neira, S.2
  • 10
    • 0029111403 scopus 로고
    • The β-selective (4/1) phosphorylation of 2,3,4,6-tetra-O-acetylmannopyranose with limiting diphenyl chlorophosphidate has been reported: Sabesan, S.; Neira, S. Carbohydr. Res. 1992, 223, 169-185. It is highly unlikely that this method can be extended to the significantly less reactive dialkyl chlorophosphidates required for the synthesis of the present targets. Other groups typically report α-selective phosphorylation of mannose in this type of process even with diphenyl chlorophosphidate, e.g., Boger, D. L.; Teramoto, S.; Zhou, J. J. Am. Chem. Soc. 1995, 117, 7344-7356.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 7344-7356
    • Boger, D.L.1    Teramoto, S.2    Zhou, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.