SCOPUS 정보 검색 플랫폼

Volumn 41, Issue 45, 2000, Pages 8753-8758

Can preferential β-mannopyranoside formation with 4,6-O-benzylidene protected mannopyranosyl sulfoxides be reached with trichloroacetimidates?

(2) Weingart, R a Schmidt, R R a

a UNIVERSITY OF KONSTANZ (Germany)

Author keywords

Glycosidation; Glycosyl donors; N glycans; Sulfoxides; Trichloroacetimidates; mannopyranosides

Indexed keywords

3 O ALLYL 2 O BENZYL 4,6 O BENZYLIDENE ALPHA DEXTRO MANNOPYRANOSYL SULFOXIDE; BENZYLIDENE DERIVATIVE; BETA MANNOPYRANOSIDE; CHLORINE DERIVATIVE; GLYCAN DERIVATIVE; GLYCOSIDE; MANNOSE; PYRANOSIDE; SOLVENT; TRICHLOROACETIMIDIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CONCENTRATION RESPONSE; GLYCOSYLATION; PARAMETER; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0034605825 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)01497-0 Document Type: Article

Times cited : (121)

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