Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David Crich

Showing results (11-20 of 272) with videos related to

Pageof 28
Sort By:
Organic Letters|April 29, 2020
Synthesis of Gentamicin Minor Components: Gentamicin B1 and Gentamicin X2Parasuraman Rajasekaran, David Crich
Carbohydrate 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 Crich
Organic Letters|February 28, 2003
Direct synthesis of the beta-l-rhamnopyranosidesDavid Crich, John Picione
Journal 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 Yao
Angewandte Chemie (International Ed. in English)|March 25, 2010
Stereoselective synthesis of alpha-keto-deoxy-D-glycero-D-galacto-nonulosonic acid glycosides by means of the 4,5-O-carbonate protecting groupDavid Crich, Chandrasekhar Navuluri
The 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 Jayalath
Organic Letters|March 25, 2005
Synthesis and stereoselective glycosylation of D- and L-glycero-beta-D-manno-heptopyranosesDavid Crich, Abhisek Banerjee
Journal 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 Banerjee
The Journal of Organic Chemistry|August 26, 2006
Expedient synthesis of threo-beta-hydroxy-alpha-amino acid derivatives: phenylalanine, tyrosine, histidine, and tryptophanDavid Crich, Abhisek Banerjee
The Journal of Organic Chemistry|March 7, 2007
O-sialylation with N-acetyl-5-n,4-o-carbonyl-protected thiosialoside donors in dichloromethane: facile and selective cleavage of the oxazolidinone ringDavid Crich, Wenju Li
Pageof 28

Showing results (11-20 of 272) with videos related to

Sort By:
Pageof 28
Organic Letters|April 29, 2020
Synthesis of Gentamicin Minor Components: Gentamicin B1 and Gentamicin X2Parasuraman Rajasekaran, David Crich
Carbohydrate 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 Crich
Organic Letters|February 28, 2003
Direct synthesis of the beta-l-rhamnopyranosidesDavid Crich, John Picione
Journal 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 Yao
Angewandte Chemie (International Ed. in English)|March 25, 2010
Stereoselective synthesis of alpha-keto-deoxy-D-glycero-D-galacto-nonulosonic acid glycosides by means of the 4,5-O-carbonate protecting groupDavid Crich, Chandrasekhar Navuluri
The 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 Jayalath
Organic Letters|March 25, 2005
Synthesis and stereoselective glycosylation of D- and L-glycero-beta-D-manno-heptopyranosesDavid Crich, Abhisek Banerjee
Journal 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 Banerjee
The Journal of Organic Chemistry|August 26, 2006
Expedient synthesis of threo-beta-hydroxy-alpha-amino acid derivatives: phenylalanine, tyrosine, histidine, and tryptophanDavid Crich, Abhisek Banerjee
The Journal of Organic Chemistry|March 7, 2007
O-sialylation with N-acetyl-5-n,4-o-carbonyl-protected thiosialoside donors in dichloromethane: facile and selective cleavage of the oxazolidinone ringDavid Crich, Wenju Li
Pageof 28