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David Crich

Showing results (181-190 of 272) with videos related to

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Accounts of Chemical Research|May 11, 2007
Catalysis of stannane-mediated radical chain reactions by benzeneselenolDavid Crich, Daniel Grant, Venkataramanan Krishnamurthy, et al.
Organic Letters|July 3, 2013
Se-(9-Fluorenylmethyl) selenoesters; preparation, reactivity, and use as convenient synthons for selenoacidsFabien Fécourt, Bernard Delpech, Oleg Melnyk, et al.
The Journal of Organic Chemistry|October 11, 2003
Influence of the 4,6-O-benzylidene, 4,6-O-phenylboronate, and 4,6-O-polystyrylboronate protecting groups on the stereochemical outcome of thioglycoside-based glycosylations mediated by 1-benzenesulfinyl piperidine/triflic anhydride and N-iodosuccinimide/trimethylsilyl triflateDavid Crich, Marco de la Mora, A U Vinod
Carbohydrate Research|March 29, 2020
Stereospecific synthesis of methyl 2-amino-2,4-dideoxy-6S-deuterio-α-D-xylo-hexopyranoside and methyl 2-amino-2,4-dideoxy-6S-deuterio-4-propyl-α-d-glucopyranoside: Side chain conformation of the novel aminoglycoside antibiotic propylamycinMichael G Pirrone, Takahiko Matsushita, Andrea Vasella, et al.
Angewandte Chemie (International Ed. in English)|December 3, 2014
The isothiocyanato moiety: an ideal protecting group for the stereoselective synthesis of sialic acid glycosides and subsequent diversificationAppi Reddy Mandhapati, Salla Rajender, Jonathan Shaw, et al.
The Journal of Organic Chemistry|March 25, 2011
Protecting group-free glycoligation by the desulfurative rearrangement of allylic disulfides as a means of assembly of oligosaccharide mimeticsVenkataraman Subramanian, Myriame Moumé-Pymbock, Tianshun Hu, et al.
Journal of the American Chemical Society|August 30, 2013
Probing the influence of a 4,6-O-acetal on the reactivity of galactopyranosyl donors: verification of the disarming influence of the trans-gauche conformation of C5-C6 bondsMyriame Moumé-Pymbock, Takayuki Furukawa, Sujit Mondal, et al.
Carbohydrate Research|March 10, 2023
Synthesis and evaluation of 1,5-dithialaminaribiose and -triose tetravalent constructsDaniil Ahiadorme, Chennaiah Ande, Rafael Fernandez-Botran, et al.
Carbohydrate Research|March 16, 2020
Use of hydroxylamines, hydroxamic acids, oximes and amines as nucleophiles in the Zbiral oxidative deamination of N-acetyl neuraminic acid. Isolation and characterization of novel mono- and disubstitution productsMohammed Hawsawi, Michael G Pirrone, Anura Wickramasinghe, et al.
ACS Medicinal Chemistry Letters|April 15, 2026
Endocyclic Trisubstituted Hydroxylamine Isosteres of Basic Amines for ADME Modulation and Reduction of hERG ActivityIftikhar Khan, Asiri A Hettikankanamalage, Yizhi Cui, et al.
Pageof 28

Showing results (181-190 of 272) with videos related to

Sort By:
Pageof 28
Accounts of Chemical Research|May 11, 2007
Catalysis of stannane-mediated radical chain reactions by benzeneselenolDavid Crich, Daniel Grant, Venkataramanan Krishnamurthy, et al.
Organic Letters|July 3, 2013
Se-(9-Fluorenylmethyl) selenoesters; preparation, reactivity, and use as convenient synthons for selenoacidsFabien Fécourt, Bernard Delpech, Oleg Melnyk, et al.
The Journal of Organic Chemistry|October 11, 2003
Influence of the 4,6-O-benzylidene, 4,6-O-phenylboronate, and 4,6-O-polystyrylboronate protecting groups on the stereochemical outcome of thioglycoside-based glycosylations mediated by 1-benzenesulfinyl piperidine/triflic anhydride and N-iodosuccinimide/trimethylsilyl triflateDavid Crich, Marco de la Mora, A U Vinod
Carbohydrate Research|March 29, 2020
Stereospecific synthesis of methyl 2-amino-2,4-dideoxy-6S-deuterio-α-D-xylo-hexopyranoside and methyl 2-amino-2,4-dideoxy-6S-deuterio-4-propyl-α-d-glucopyranoside: Side chain conformation of the novel aminoglycoside antibiotic propylamycinMichael G Pirrone, Takahiko Matsushita, Andrea Vasella, et al.
Angewandte Chemie (International Ed. in English)|December 3, 2014
The isothiocyanato moiety: an ideal protecting group for the stereoselective synthesis of sialic acid glycosides and subsequent diversificationAppi Reddy Mandhapati, Salla Rajender, Jonathan Shaw, et al.
The Journal of Organic Chemistry|March 25, 2011
Protecting group-free glycoligation by the desulfurative rearrangement of allylic disulfides as a means of assembly of oligosaccharide mimeticsVenkataraman Subramanian, Myriame Moumé-Pymbock, Tianshun Hu, et al.
Journal of the American Chemical Society|August 30, 2013
Probing the influence of a 4,6-O-acetal on the reactivity of galactopyranosyl donors: verification of the disarming influence of the trans-gauche conformation of C5-C6 bondsMyriame Moumé-Pymbock, Takayuki Furukawa, Sujit Mondal, et al.
Carbohydrate Research|March 10, 2023
Synthesis and evaluation of 1,5-dithialaminaribiose and -triose tetravalent constructsDaniil Ahiadorme, Chennaiah Ande, Rafael Fernandez-Botran, et al.
Carbohydrate Research|March 16, 2020
Use of hydroxylamines, hydroxamic acids, oximes and amines as nucleophiles in the Zbiral oxidative deamination of N-acetyl neuraminic acid. Isolation and characterization of novel mono- and disubstitution productsMohammed Hawsawi, Michael G Pirrone, Anura Wickramasinghe, et al.
ACS Medicinal Chemistry Letters|April 15, 2026
Endocyclic Trisubstituted Hydroxylamine Isosteres of Basic Amines for ADME Modulation and Reduction of hERG ActivityIftikhar Khan, Asiri A Hettikankanamalage, Yizhi Cui, et al.
Pageof 28