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Volumn 15, Issue 1, 2009, Pages 53-57

Fast access to robust C-sialoside multimers

Author keywords

Click reaction; Cycloaddition; Glycoconjugates; Samarium; Sialic acids

Indexed keywords

ACETYLENE; ACIDS; CARBOXYLIC ACIDS; CELL MEMBRANES; KETONES; SAMARIUM;

EID: 58449131233     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200801810     Document Type: Article
Times cited : (29)

References (47)
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    • For a very recent clustering of 5-sialosides to calix[4]arene scaffolds see: A. Marra, L. Moni, D. Pazzi, A. Corallini, D. Bridib, A. Dondoni, Org. Biomot. Chem. 2008, 6, 1396-1409.
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    • The bromo-azides were prepared by treating an excess of the corresponding dibromoalcanes with sodium azide in DMF at 80°C overnight 46-65, yield
    • The bromo-azides were prepared by treating an excess of the corresponding dibromoalcanes with sodium azide in DMF at 80°C overnight (46-65 % yield).
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    • Propargylation of this scaffold will be described in a full paper
    • Propargylation of this scaffold will be described in a full paper.
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    • An interesting notable exception was the preparation of tetravalent 10 which did not show the formation of intermediate lower oligomers
    • An interesting notable exception was the preparation of tetravalent 10 which did not show the formation of intermediate lower oligomers.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.