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Volumn 13, Issue 35, 2007, Pages 9757-9774

Chemical clockwise tridifferentiation of α- and β-cyclodextrins: Bascule-bridge or deoxy-sugars strategies

Author keywords

Aluminum; Concave molecules; Cyclodextrins oligosaccharides; Regioselectivity

Indexed keywords

ALUMINUM COMPOUNDS; ENZYMES; MOLECULAR DYNAMICS; OLIGOSACCHARIDES; REGIOSELECTIVITY;

EID: 37249086730     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200700971     Document Type: Article
Times cited : (50)

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    • A notable exception, that works on both α- and β-CD: D. Armspach, L. Poorters, D. Matt, B. Benmerad, F. Balegroune, L. Toupet, Org. Biomol. Chem. 2005, 3, 2588-2592.
    • A notable exception, that works on both α- and β-CD: D. Armspach, L. Poorters, D. Matt, B. Benmerad, F. Balegroune, L. Toupet, Org. Biomol. Chem. 2005, 3, 2588-2592.
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    • Our experience now shows that the best protocol to operate this reaction is the use of 30 equivalents of DIBAL-H at a 1 M concentration in freshly distilled anhydrous toluene, at 50°C during 2 h, and under a flow of argon concentrating the reaction upon time
    • Our experience now shows that the best protocol to operate this reaction is the use of 30 equivalents of DIBAL-H at a 1 M concentration in freshly distilled anhydrous toluene, at 50°C during 2 h, and under a flow of argon concentrating the reaction upon time.
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    • Detailed structural elucidation can be found as Supporting Information
    • Detailed structural elucidation can be found as Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.