Synthesis of a 28-mer oligosaccharide core of Mycobacterial lipoarabinomannan (LAM) requires only two n-pentenyl orthoester progenitors

Tetrahedron Asymmetry

Volumn 17, Issue 17, 2006, Pages 2449-2463

  Fraser Reid, Bert ^a   Lu, Jun ^a   Jayaprakash, K N ^a   López, J Cristóbal ^a  

^a Natural Products and Glycotechnology Research Institute Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARABINOSE; CARBOHYDRATE; ESTER; GLYCOSIDE; HYDROXIDE; INOSITOL; LANTHANIDE; LIPOARABINOMANNAN; MANNAN; MANNOSE; N IODOSUCCINIMIDE; N PENTENYL GLYCOSIDE; N PENTENYL ORTHOESTER; OLIGOSACCHARIDE; SUCCINIMIDE DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG; YTTERBIUM;

CHEMICAL STRUCTURE; GLYCOSIDATION; GLYCOSYLATION; LABORATORY APPARATUS, EQUIPMENT AND SUPPLIES; MEDICAL RESEARCH; MOLECULAR BIOLOGY; MOLECULAR WEIGHT; MYCOBACTERIUM; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; REVIEW; STRUCTURE ANALYSIS; SYNTHESIS; TUBERCULOSIS;

EID: 33750987650     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.09.008     Document Type: Review

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