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David Crich

Showing results (31-40 of 272) with videos related to

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Organic Letters|November 9, 2002
Fluorous dimethyl sulfide: a convenient, odorless, recyclable borane carrierDavid Crich, Santhosh Neelamkavil
Journal of the American Chemical Society|October 17, 2002
Diastereoselectivity in the cyclization of alkene radical cations generated under non-oxidizing conditions: contact ion pairs and memory effectsDavid Crich, Krishnakumar Ranganathan
Organic Letters|June 7, 2003
The 4,6-O-[alpha-(2-(2- iodophenyl)ethylthiocarbonyl)benzylidene] protecting group: stereoselective glycosylation, reductive radical fragmentation, and synthesis of beta-D-rhamnopyranosides and other deoxy sugarsDavid Crich, Qingjia Yao
Journal of the American Chemical Society|July 26, 2002
Solid-phase synthesis of beta-mannosidesDavid Crich, Mark Smith
Tetrahedron|December 4, 2018
Allylic Strain as a Stereocontrol Element in the Hydrogenation of 3-Hydroxymethyl-cyclohex-3-en-1,2,5-triol Derivatives. Synthesis of the Carbasugar Pseudo-2-deoxy-α-D-glucopyranosePeng Wen, David Crich
The Journal of Organic Chemistry|April 13, 2005
Catalytic oxidation adjacent to carbonyl groups and at benzylic positions with a fluorous seleninic acid in the presence of iodoxybenzeneDavid Crich, Yekui Zou
Organic Letters|May 20, 2005
2-O-propargyl ethers: readily cleavable, minimally intrusive protecting groups for beta-mannosyl donorsDavid Crich, Prasanna Jayalath
Organic Letters|October 6, 2006
1-naphthylpropargyl ether group: a readily cleaved and sterically minimal protecting system for stereoselective glycosylationDavid Crich, Baolin Wu
Chimia|April 8, 2011
Synthesis of the beta-rhamnopyranosides and the 6-deoxy-beta-mannoheptopyranosidesSébastien Picard, David Crich
Organic Letters|October 2, 2008
Is donor-acceptor hydrogen bonding necessary for 4,6-O-benzylidene-directed beta-mannopyranosylation? Stereoselective synthesis of beta-C-mannopyranosides and alpha-C-glucopyranosidesDavid Crich, Indrajeet Sharma
Pageof 28

Showing results (31-40 of 272) with videos related to

Sort By:
Pageof 28
Organic Letters|November 9, 2002
Fluorous dimethyl sulfide: a convenient, odorless, recyclable borane carrierDavid Crich, Santhosh Neelamkavil
Journal of the American Chemical Society|October 17, 2002
Diastereoselectivity in the cyclization of alkene radical cations generated under non-oxidizing conditions: contact ion pairs and memory effectsDavid Crich, Krishnakumar Ranganathan
Organic Letters|June 7, 2003
The 4,6-O-[alpha-(2-(2- iodophenyl)ethylthiocarbonyl)benzylidene] protecting group: stereoselective glycosylation, reductive radical fragmentation, and synthesis of beta-D-rhamnopyranosides and other deoxy sugarsDavid Crich, Qingjia Yao
Journal of the American Chemical Society|July 26, 2002
Solid-phase synthesis of beta-mannosidesDavid Crich, Mark Smith
Tetrahedron|December 4, 2018
Allylic Strain as a Stereocontrol Element in the Hydrogenation of 3-Hydroxymethyl-cyclohex-3-en-1,2,5-triol Derivatives. Synthesis of the Carbasugar Pseudo-2-deoxy-α-D-glucopyranosePeng Wen, David Crich
The Journal of Organic Chemistry|April 13, 2005
Catalytic oxidation adjacent to carbonyl groups and at benzylic positions with a fluorous seleninic acid in the presence of iodoxybenzeneDavid Crich, Yekui Zou
Organic Letters|May 20, 2005
2-O-propargyl ethers: readily cleavable, minimally intrusive protecting groups for beta-mannosyl donorsDavid Crich, Prasanna Jayalath
Organic Letters|October 6, 2006
1-naphthylpropargyl ether group: a readily cleaved and sterically minimal protecting system for stereoselective glycosylationDavid Crich, Baolin Wu
Chimia|April 8, 2011
Synthesis of the beta-rhamnopyranosides and the 6-deoxy-beta-mannoheptopyranosidesSébastien Picard, David Crich
Organic Letters|October 2, 2008
Is donor-acceptor hydrogen bonding necessary for 4,6-O-benzylidene-directed beta-mannopyranosylation? Stereoselective synthesis of beta-C-mannopyranosides and alpha-C-glucopyranosidesDavid Crich, Indrajeet Sharma
Pageof 28