Direct Chemical Synthesis of the β-Mannans: Linear and Block Syntheses of the Alternating β-(1→3)-β-(1→4)-Mannan Common to <i>Rhodotorula </i><i>glutinis</i>, <i>Rhodotorula </i><i>mucilaginosa</i>, and <i>Leptospira </i><i>biflexa</i>David Crich, Hongmei Li, Wenju Li|Journal of the American Chemical Society|2004Cited by 101
Direct Stereoselective Synthesis of β-ThiomannosidesDavid Crich, Hongmei Li|The Journal of Organic Chemistry|2000Cited by 74
Direct Synthesis of β-Mannans. A Hexameric [→3)-β-<scp>d</scp>-Man-(1→4)-β-<scp>d</scp>-Man-(1]<sub>3</sub> Subunit of the Antigenic Polysaccharides from <i>Leptospira </i><i>b</i><i>iflexa</i> and the Octameric (1→2)-Linked β-<scp>d</scp>-Mannan of the <i>Candida a</i><i>lbicans</i> Phospholipomannan. X-ray Crystal Structure of a Protected TetramerDavid Crich, Arnold L. Rheingold, Roger D. Sommer et al.|Journal of the American Chemical Society|2001Cited by 72
Synthesis of the Salmonella Type E<sub>1</sub> Core Trisaccharide as a Probe for the Generality of 1-(Benzenesulfinyl)piperidine/Triflic Anhydride Combination for Glycosidic Bond Formation from ThioglycosidesDavid Crich, Hongmei Li|The Journal of Organic Chemistry|2002Cited by 50
Stereodirecting Effect of Esters at the 4-Position of Galacto- and Glucopyranosyl Donors: Effect of 4-<i>C</i>-Methylation on Side-Chain Conformation and Donor Reactivity, and Influence of Concentration and Stoichiometry on Distal Group ParticipationAnde Chennaiah, David Crich|The Journal of Organic Chemistry|2023Cited by 16