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The Journal of Organic Chemistry|January 10, 2009
Stereocontrolled synthesis of D- and L-beta-rhamnopyranosides with 4-O-6-S-alpha-cyanobenzylidene-protected 6-thiorhamnopyranosyl thioglycosidesDavid Crich, Linfeng LiJournal of the American Chemical Society|April 11, 2020
Stereocontrolled Synthesis of the Equatorial Glycosides of 3-Deoxy-d-manno-oct-2-ulosonic Acid: Role of Side Chain ConformationPhilemon Ngoje, David CrichOrganic Letters|April 29, 2020
Synthesis of Gentamicin Minor Components: Gentamicin B1 and Gentamicin X2Parasuraman Rajasekaran, David CrichCarbohydrate Research|October 17, 2016
Synthesis and intramolecular glycosylation of sialyl mono-esters of o-xylylene glycol. The importance of donor configuration and nitrogen protecting groups on cyclization yield and selectivity; isolation and characterization of a N-sialyl acetamide indicative of participation by acetonitrileHarsha Amarasekara, David CrichOrganic Letters|February 28, 2003
Direct synthesis of the beta-l-rhamnopyranosidesDavid Crich, John PicioneJournal of the American Chemical Society|July 1, 2004
Benzylidene acetal fragmentation route to 6-deoxy sugars: direct reductive cleavage in the presence of ether protecting groups, permitting the efficient, highly stereocontrolled synthesis of beta-D-rhamnosides from D-mannosyl glycosyl donors. Total synthesis of alpha-D-Gal-(1-->3)-alpha-D-Rha-(1-->3)- beta-D-Rha-(1-->4)-beta-D-Glu-OMe, the repeating unit of the antigenic lipopolysaccharide from Escherichia hermannii ATCC 33650 and 33652David Crich, Qingjia YaoThe Journal of Organic Chemistry|August 27, 2005
Stereocontrolled formation of beta-glucosides and related linkages in the absence of neighboring group participation: influence of a trans-fused 2,3-O-carbonate groupDavid Crich, Prasanna JayalathOrganic Letters|March 25, 2005
Synthesis and stereoselective glycosylation of D- and L-glycero-beta-D-manno-heptopyranosesDavid Crich, Abhisek BanerjeeJournal of the American Chemical Society|June 15, 2006
Stereocontrolled synthesis of the D- and L-glycero-beta-D-manno-heptopyranosides and their 6-deoxy analogues. Synthesis of methyl alpha-l-rhamno-pyranosyl-(1-->3)-D-glycero-beta-D-manno-heptopyranosyl- (1-->3)-6-deoxy-glycero-beta-D-manno-heptopyranosyl-(1-->4)-alpha-L- rhamno-pyranoside, a tetrasaccharide subunit of the lipopolysaccharide from Plesimonas shigelloidesDavid Crich, Abhisek BanerjeeThe Journal of Organic Chemistry|August 26, 2006
Expedient synthesis of threo-beta-hydroxy-alpha-amino acid derivatives: phenylalanine, tyrosine, histidine, and tryptophanDavid Crich, Abhisek BanerjeePageof 27