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Volumn 24, Issue 2, 2005, Pages 161-168

Synthesis of α-2-deoxyglycosides by acid-mediated conjugate addition

Author keywords

2 Deoxyglycosides; Conjugate addition

Indexed keywords


EID: 27844506623     PISSN: 07328303     EISSN: 15322327     Source Type: Journal    
DOI: 10.1081/CAR-200059931     Document Type: Conference Paper
Times cited : (9)

References (10)
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  • 3
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    • Studies of the stereoselective reduction of keto sugar (hexosulose)
    • Stereoselective reduction: Chang, C.T.; Hui, Y.; Elchert, B. Studies of the stereoselective reduction of keto sugar (hexosulose). Tetrahedron Lett. 2001, 42, 7019-7023.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 7019-7023
    • Chang, C.T.1    Hui, Y.2    Elchert, B.3
  • 4
    • 27844578545 scopus 로고    scopus 로고
    • Functionalized saccharides
    • Boons, G.J., Ed.; Blackie Academic and Professional: London
    • Reductive amination: Boons, G.J.; Heskamp, B. Functionalized saccharides. In Carbohydrate Chemistry; Boons, G.J., Ed.; Blackie Academic and Professional: London, 1998; 56-57.
    • (1998) Carbohydrate Chemistry , pp. 56-57
    • Boons, G.J.1    Heskamp, B.2
  • 5
    • 6444236860 scopus 로고
    • Synthesis of branched chain sugars
    • Branching: Yoshimura, J. Synthesis of branched chain sugars. Adv. Carbohydr. Chem. Biochem. 1984, 42, 69-134.
    • (1984) Adv. Carbohydr. Chem. Biochem. , vol.42 , pp. 69-134
    • Yoshimura, J.1
  • 6
    • 0027304545 scopus 로고
    • A new stereoselective route to branched-chain nitro and amino sugars. Synthesis of both enantiomers of decilonitrose and avidinosamine
    • Branched-chain nitro and amino groups: Greven, R.; Jütten, P.; Scharf, H.D. A new stereoselective route to branched-chain nitro and amino sugars. Synthesis of both enantiomers of decilonitrose and avidinosamine. J. Org. Chem. 1993, 58, 3742-3747.
    • (1993) J. Org. Chem. , vol.58 , pp. 3742-3747
    • Greven, R.1    Jütten, P.2    Scharf, H.D.3
  • 7
    • 0018125477 scopus 로고
    • A new synthesis of methyl α-L-mycaroside
    • (a) Thiem, J.; Elvers, J. A new synthesis of methyl α-L-mycaroside. Chem. Ber. 1978, 111, 3514;
    • (1978) Chem. Ber. , vol.111 , pp. 3514
    • Thiem, J.1    Elvers, J.2
  • 8
    • 0029999934 scopus 로고    scopus 로고
    • Michael-type addition in the synthesis of α-O and -S-2-deoxyglycosides
    • (b) Michael, K.; Kessler, H. Michael-type addition in the synthesis of α-O and -S-2-deoxyglycosides. Tetrahedron Lett. 1996, 37, 3453-3456.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3453-3456
    • Michael, K.1    Kessler, H.2
  • 9
    • 0001527970 scopus 로고
    • Oxidation of fully protected glycals by hypervalent iodine reagents
    • Kirschning, A. Oxidation of fully protected glycals by hypervalent iodine reagents. J. Org. Chem. 1995, 60, 1228-1232.
    • (1995) J. Org. Chem. , vol.60 , pp. 1228-1232
    • Kirschning, A.1
  • 10
    • 0000588043 scopus 로고
    • Convenient synthesis of hex-1-enopyran-3-uloses selective oxidation of allylic alcohols using pyridinium dichromate
    • Czernecki, S.; Vijayakumaran, K.; Ville, G. Convenient synthesis of hex-1-enopyran-3-uloses selective oxidation of allylic alcohols using pyridinium dichromate. J. Org. Chem. 1986, 51, 5472-5475.
    • (1986) J. Org. Chem. , vol.51 , pp. 5472-5475
    • Czernecki, S.1    Vijayakumaran, K.2    Ville, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.