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Thomas K Hutton

Showing results (1-10 of 7) with videos related to

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The Journal of Organic Chemistry|April 8, 2006
Enhanced diastereoselectivity in beta-mannopyranosylation through the use of sterically minimal propargyl ether protecting groupsDavid Crich, Prasanna Jayalath, Thomas K Hutton
The Journal of Organic Chemistry|September 10, 2005
Is there a homolytic substitution chemistry (SH2) of sulfones?David Crich, Thomas K Hutton, Krishnakumar Ranganathan
Tetrahedron|August 22, 2007
β-Selective Glucosylation in the Absence of Neighboring Group Participation: Influence of the 3,4-O-Bisacetal Protecting SystemDavid Crich, Venkataraman Subramanian, Thomas K Hutton
Journal of the American Chemical Society|February 24, 2006
Allylic selenosulfide rearrangement: a method for chemical ligation to cysteine and other thiolsDavid Crich, Venkataramanan Krishnamurthy, Thomas K Hutton
Organic Letters|July 6, 2002
Samarium(II)-mediated reactions of gamma,delta-unsaturated ketones. Cyclization and fragmentation processesThomas K Hutton, Kenneth Muir, David J Procter
Organic Letters|December 5, 2003
Switching between novel samarium(II)-mediated cyclizations by a simple change in alcohol cosolventThomas K Hutton, Kenneth W Muir, David J Procter
Journal of the American Chemical Society|July 28, 2007
Dechalcogenative allylic selenosulfide and disulfide rearrangements: complementary methods for the formation of allylic sulfides in the absence of electrophiles. Scope, limitations, and application to the functionalization of unprotected peptides in aqueous mediaDavid Crich, Venkataramanan Krishnamurthy, Franck Brebion, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The Journal of Organic Chemistry|April 8, 2006
Enhanced diastereoselectivity in beta-mannopyranosylation through the use of sterically minimal propargyl ether protecting groupsDavid Crich, Prasanna Jayalath, Thomas K Hutton
The Journal of Organic Chemistry|September 10, 2005
Is there a homolytic substitution chemistry (SH2) of sulfones?David Crich, Thomas K Hutton, Krishnakumar Ranganathan
Tetrahedron|August 22, 2007
β-Selective Glucosylation in the Absence of Neighboring Group Participation: Influence of the 3,4-O-Bisacetal Protecting SystemDavid Crich, Venkataraman Subramanian, Thomas K Hutton
Journal of the American Chemical Society|February 24, 2006
Allylic selenosulfide rearrangement: a method for chemical ligation to cysteine and other thiolsDavid Crich, Venkataramanan Krishnamurthy, Thomas K Hutton
Organic Letters|July 6, 2002
Samarium(II)-mediated reactions of gamma,delta-unsaturated ketones. Cyclization and fragmentation processesThomas K Hutton, Kenneth Muir, David J Procter
Organic Letters|December 5, 2003
Switching between novel samarium(II)-mediated cyclizations by a simple change in alcohol cosolventThomas K Hutton, Kenneth W Muir, David J Procter
Journal of the American Chemical Society|July 28, 2007
Dechalcogenative allylic selenosulfide and disulfide rearrangements: complementary methods for the formation of allylic sulfides in the absence of electrophiles. Scope, limitations, and application to the functionalization of unprotected peptides in aqueous mediaDavid Crich, Venkataramanan Krishnamurthy, Franck Brebion, et al.
Pageof 1