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Volumn 19, Issue 16, 2008, Pages 1919-1933

Synthesis of new mono- and disaccharidic carboxymethylglycoside lactones (CMGLs) and their use toward 1,2-bisfunctionalized carbohydrate synthons

Author keywords

[No Author keywords available]

Indexed keywords

(TERT BUTYLOXYCARBONYL)METHYL 2 ACETAMIDO 3,4,6 TETRA O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO FUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO GALACTOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO GLUCOPYRANOSYL (1-4) 2,3,6 TRI O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO GLUCOPYRANOSYL (1-4) 2,3,6 TRI O ACETYL BETA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO MANNOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO FUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GALACTOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GALACTOPYRANOSYL (1-4) 2,3,6 TRI O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GALACTOPYRANOSYL (1-4) 2,3,6 TRI O ACETYL BETA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GLUCOPYRANOSYL (1-4) 2,3,6 TRI O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; (TERT BUTYLOXYCARBONYL)METHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO MANNOPYRANOSIDE; AMINE; CABOXYMETHYLGLYCOSIDE LACTONE DERIVATIVE; CARBOHYDRATE; CARBOXYMETHYL 2 ACETAMIDO 3,4,6 TETRA O ACETYL 2 DEOXY ALPHA DEXTRO GLUCOPYRANOSIDE; CARBOXYMETHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO GLUCOPYRANOSYL(1-4) 2,3,6 TRI O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; CARBOXYMETHYL 2,3,4,6 TETRA O ACETYL ALPHA DEXTRO GLUCOPYRANOSYL(1-4) 2,3,6 TRI O ACETYL BETA DEXTRO GLUCOPYRANOSIDE; CARBOXYMETHYL 2,3,4,6 TETRA O ACETYL ALPHA LEVO FUCOOPYRANOSIDE; CARBOXYMETHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GALACTOPYRANOSYL(1-4) 2,3,6 TRI O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; CARBOXYMETHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GALACTOPYRANOSYL(1-4) 2,3,6 TRI O ACETYL BETA DEXTRO GLUCOPYRANOSIDE; CARBOXYMETHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO GLUCOPYRANOSYL(1-4) 2,3,6 TRI O ACETYL ALPHA DEXTRO GLUCOPYRANOSIDE; CARBOXYMETHYL 2,3,4,6 TETRA O ACETYL BETA DEXTRO MANNOPYRANOSIDE; DISACCHARIDE; GLYCOSIDE; HYDROXIDE; LACTONE DERIVATIVE; MONOSACCHARIDE; UNCLASSIFIED DRUG;

EID: 50949107488     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.07.016     Document Type: Article
Times cited : (23)

References (52)
  • 3
    • 0000109163 scopus 로고    scopus 로고
    • Ernst B., Hart G.W., and Sinaÿ P. (Eds), Wiley-CCH, Weinheim, Germany
    • Wessel H.P. In: Ernst B., Hart G.W., and Sinaÿ P. (Eds). Carbohydrates in Chemistry and Biology Vol. 1 (2000), Wiley-CCH, Weinheim, Germany 565-585
    • (2000) Carbohydrates in Chemistry and Biology , vol.1 , pp. 565-585
    • Wessel, H.P.1
  • 4
    • 0012235012 scopus 로고    scopus 로고
    • Fraser-Reid B.O., Tatsuta K., and Thiem J. (Eds), Springer, Heidelberg, Germany
    • Wessel H.P. In: Fraser-Reid B.O., Tatsuta K., and Thiem J. (Eds). GlycoScience: Chemistry and Chemical Biology, Part II (2001), Springer, Heidelberg, Germany 2725-2752
    • (2001) GlycoScience: Chemistry and Chemical Biology, Part II , pp. 2725-2752
    • Wessel, H.P.1
  • 30
    • 44949238684 scopus 로고    scopus 로고
    • For a recent reference, see:
    • For a recent reference, see:. Li Y., Tang P., Chen Y., and Yu B. J. Org. Chem. 73 (2008) 4323-4325
    • (2008) J. Org. Chem. , vol.73 , pp. 4323-4325
    • Li, Y.1    Tang, P.2    Chen, Y.3    Yu, B.4
  • 34
    • 0002644010 scopus 로고    scopus 로고
    • Kahn S.H., and O'Neill R.A. (Eds), Hardwood Academic Publishers
    • Schmidt R.R. In: Kahn S.H., and O'Neill R.A. (Eds). Modern Methods in Carbohydrate Synthesis (1996), Hardwood Academic Publishers 20-54
    • (1996) Modern Methods in Carbohydrate Synthesis , pp. 20-54
    • Schmidt, R.R.1
  • 41
    • 50949097775 scopus 로고    scopus 로고
    • note
    • Differing results reported in Refs. 21 and 25 concerning the reaction of N-acyl glucosamines with allyl bromide suggest that concentration and solubility play important roles in the selectivity outcome of this reaction.
  • 42
    • 33947493431 scopus 로고    scopus 로고
    • For a recent review on carbohydrate-based substrates used in Huisgen cycloadditions, see:
    • For a recent review on carbohydrate-based substrates used in Huisgen cycloadditions, see:. Dedola S., Nepogodiev S.A., and Field R.A. Org. Biomol. Chem. 5 (2007) 1006-1017
    • (2007) Org. Biomol. Chem. , vol.5 , pp. 1006-1017
    • Dedola, S.1    Nepogodiev, S.A.2    Field, R.A.3
  • 43
    • 45449117868 scopus 로고    scopus 로고
    • Queneau, Y.; Chambert, S.; Besset, C.; Cheaib, R. Carbohydr. Res. 2008, in press, doi.org/10.1016/j.carres.2008.02.008.
    • Queneau, Y.; Chambert, S.; Besset, C.; Cheaib, R. Carbohydr. Res. 2008, in press, doi.org/10.1016/j.carres.2008.02.008.
  • 51
    • 50949089956 scopus 로고    scopus 로고
    • Sasaki, A.; Naoichi, M. JP Patent 06271597.
    • Sasaki, A.; Naoichi, M. JP Patent 06271597.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.