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Volumn , Issue 9, 2000, Pages 1759-1765

Synthesis and α-mannosidase inhibitory activity of three deoxy derivatives of mannostatin A

Author keywords

Aminocyclitols; Cyclitols; Deoxygenation; Glycosidase inhibitors; Mannosidase inhibitors

Indexed keywords

ALPHA MANNOSIDASE; AMINOCYCLITOL; GLYCOSIDASE INHIBITOR; MANNOSTATIN A;

EID: 0034027097     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0690(200005)2000:9<1759::AID-EJOC1759>3.0.CO;2-J     Document Type: Article
Times cited : (19)

References (23)
  • 5
    • 0029058703 scopus 로고
    • Total synthesis: [3a] S. Ogawa, Y. Yuming, J. Chem. Soc., Chem. Cummun. 1991, 890-891; Biorg. Med. Chem. 1995, 3, 939-943. -
    • (1995) Biorg. Med. Chem. , vol.3 , pp. 939-943
  • 6
    • 0025880543 scopus 로고
    • [3b] S. B. King, B. Ganem, J. Am. Chem. Soc. 1991, 113, 5089-5090; J. Am. Chem. Soc. 1994, 116, 562-571. -
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 5089-5090
    • King, S.B.1    Ganem, B.2
  • 7
    • 0028349238 scopus 로고
    • [3b] S. B. King, B. Ganem, J. Am. Chem. Soc. 1991, 113, 5089-5090; J. Am. Chem. Soc. 1994, 116, 562-571. -
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 562-571
  • 9
    • 0013604392 scopus 로고
    • [3d] B. M. Trost, D. L. Van Vranken, J. Am. Chem. Soc. 1991, 113, 5089-5090. For a review article, see B. Ganem, Carbohydrate Mimics (Ed.: Y. Chapleur), Wiley-VCH, Weinheim, 1998, pp. 239-258.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 5089-5090
    • Trost, B.M.1    Van Vranken, D.L.2
  • 10
    • 0013576151 scopus 로고    scopus 로고
    • Ed.: Y. Chapleur, Wiley-VCH, Weinheim
    • [3d] B. M. Trost, D. L. Van Vranken, J. Am. Chem. Soc. 1991, 113, 5089-5090. For a review article, see B. Ganem, Carbohydrate Mimics (Ed.: Y. Chapleur), Wiley-VCH, Weinheim, 1998, pp. 239-258.
    • (1998) Carbohydrate Mimics , pp. 239-258
    • Ganem, B.1
  • 11
    • 0000354881 scopus 로고
    • IUPAC-IUB 1973 Recommendations for Cyclitols
    • In the Experimental Section, the R,S-notation is generally used instead to describe absolute configurations
    • In this paper, the nomenclature of cyclitols follows the IUPAC-IUB 1973 Recommendations for Cyclitols [Pure Appl. Chem. 1974, 37, 285-297]. In the Experimental Section, the R,S-notation is generally used instead to describe absolute configurations.
    • (1974) Pure Appl. Chem. , vol.37 , pp. 285-297
  • 12
    • 0025675652 scopus 로고    scopus 로고
    • G. Legler, Adv. Carbohydr. Chem. Biochem. 1990, 48, 319-384; G. Legler, Carbohydrate Mimics (Ed.: Y. Chapleur), Wiley-VCH, Weinheim, 1998, pp. 463-490.
    • (1990) Adv. Carbohydr. Chem. Biochem. , vol.48 , pp. 319-384
    • Legler, G.1
  • 13
    • 0025675652 scopus 로고    scopus 로고
    • (Ed.: Y. Chapleur), Wiley-VCH, Weinheim
    • G. Legler, Adv. Carbohydr. Chem. Biochem. 1990, 48, 319-384; G. Legler, Carbohydrate Mimics (Ed.: Y. Chapleur), Wiley-VCH, Weinheim, 1998, pp. 463-490.
    • (1998) Carbohydrate Mimics , pp. 463-490
    • Legler, G.1
  • 19
    • 0342710083 scopus 로고    scopus 로고
    • note
    • Reaction conditions which facilitate the migration of the cyclohexylidene function were thus found. However, attempts have not been made to optimize the reaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.