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Volumn 9, Issue 14, 2003, Pages 3397-3414

Highly diastereoselective additions to polyhydroxylated pyrrolidine cyclic imines: Ready elaboration of aza-sugar scaffolds to create diverse carbohydrate-processing enzyme probes

Author keywords

Asymmetric synthesis; Azasugars; Carbohydrates; Enzyme catalysis; Heterocycles

Indexed keywords

ADDITION REACTIONS; AROMATIC COMPOUNDS; CONFORMATIONS; ENZYME INHIBITION; ENZYMES; NITROGEN COMPOUNDS; REACTION KINETICS; STEREOCHEMISTRY; SUGARS; SYNTHESIS (CHEMICAL);

EID: 0042848476     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200304718     Document Type: Article
Times cited : (85)

References (110)
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    • note
    • Imines 3 and 4 contain the same core substructure as ribitol imine 1 (see ref. [14]), which prior to this work had been the substrate for one of the highest yielding examples of addition of an organometallic nucleophile to a cyclic imine reported in the literature. We therefore wondered if the increased rigidity of this bicyclic [3.3.0] geometry could be an important factor.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.