Thomas K. Hutton

发表

Switching between novel samarium(II)-mediated cyclizations by a simple change in alcohol cosolvent.

D. Procter, K. Muir, Thomas K. Hutton, 2003, Organic letters.

Samarium(II)-mediated reactions of γ,δ-unsaturated ketones. Cyclization and fragmentation processes

D. Procter, K. Muir, Thomas K. Hutton, 2002 .

Allylic selenosulfide rearrangement: a method for chemical ligation to cysteine and other thiols.

Venkata R. Krishnamurthy, D. Crich, Thomas K. Hutton, 2006, Journal of the American Chemical Society.

1‐(4‐Methoxyphenyl)‐2‐(4′‐methylbenzylthio)ethylamine

L. Parker, Thomas K. Hutton, 2005 .

Disarming, non-participating 2-O-protecting groups in manno- and rhamnopyranosylation: scope and limitations of sulfonates, vinylogous esters, phosphates, cyanates, and nitrates

Abhisek Banerjee, D. Crich, Thomas K. Hutton, 2005 .

β-Selective Glucosylation in the Absence of Neighboring Group Participation: Influence of the 3,4-O-Bisacetal Protecting System.

V. Subramanian, D. Crich, Thomas K. Hutton, 2007, Tetrahedron.

β-Selective Glucosylation in the Absence of Neighboring Group Participation: Influence of the 3,4-O-Bisacetal Protecting System.

V. Subramanian, D. Crich, Thomas K. Hutton, 2007, Tetrahedron.

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 media.

Venkata R. Krishnamurthy, V. Subramanian, D. Crich, 2007, Journal of the American Chemical Society.

Is there a homolytic substitution chemistry (SH2) of sulfones?

D. Crich, Thomas K. Hutton, K. Ranganathan, 2005, Journal of Organic Chemistry.

Enhanced diastereoselectivity in beta-mannopyranosylation through the use of sterically minimal propargyl ether protecting groups.

D. Crich, Thomas K. Hutton, P. Jayalath, 2006, Journal of Organic Chemistry.