J. P. Yasomanee

发表

p-type oxide semiconductors as hole collectors in dye-sensitized solid-state solar cells

J. Bandara, J. P. Yasomanee, 2007 .

Multi-electron storage of photoenergy using Cu2O–TiO2 thin film photocatalyst

J. Bandara, J. P. Yasomanee, 2008 .

Bromine-promoted glycosidation of conformationally superarmed thioglycosides.

M. Civera, L. Belvisi, J. P. Yasomanee, 2019, Chemistry.

Synthesis of 2-azido-2-deoxy- and 2-acetamido-2-deoxy-D-manno derivatives as versatile building blocks.

J. P. Yasomanee, A. Demchenko, Yongzhen Zhang, 2019, Carbohydrate research.

OFox imidates as versatile glycosyl donors for chemical glycosylation.

Swati S. Nigudkar, K. Stine, J. P. Yasomanee, 2017, Organic & biomolecular chemistry.

Hydrogen bond mediated aglycone delivery: synthesis of linear and branched α-glucans.

J. P. Yasomanee, A. Demchenko, 2014, Angewandte Chemie.

Glycosidation of thioglycosides in the presence of bromine: mechanism, reactivity, and stereoselectivity.

J. P. Yasomanee, A. Demchenko, Sophon Kaeothip, 2012, The Journal of organic chemistry.

From Stereocontrolled Glycosylation to Expeditious Oligosaccharide Synthesis

J. P. Yasomanee, A. Demchenko, 2014 .

2,3-Di-O-picolinyl building blocks as glycosyl donors with switchable stereoselectivity.

J. P. Yasomanee, A. Demchenko, N. Rath, 2016, Organic & biomolecular chemistry.

6-O-Picolinyl and 6-O-Picoloyl Building Blocks As Glycosyl Donors with Switchable Stereoselectivity.

J. P. Yasomanee, A. Demchenko, A. K. Kayastha, 2015, Organic letters.

Hydrogen-bond-mediated aglycone delivery (HAD): a highly stereoselective synthesis of 1,2-cis α-D-glucosides from common glycosyl donors in the presence of bromine.

J. P. Yasomanee, A. Demchenko, 2015, Chemistry.

Hydrogen-bond-mediated aglycone delivery: focus on β-mannosylation.

J. P. Yasomanee, A. Demchenko, S. Pistorio, 2014, Organic letters.

Effect of remote picolinyl and picoloyl substituents on the stereoselectivity of chemical glycosylation.

J. P. Yasomanee, A. Demchenko, 2012, Journal of the American Chemical Society.

Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2.

Swati S. Nigudkar, K. Stine, J. P. Yasomanee, 2018, Organic & biomolecular chemistry.

Application of Armed, Disarmed, Superarmed, and Superdisarmed Building Blocks in Stereocontrolled Glycosylation and Expeditious Oligosaccharide Synthesis

J. P. Yasomanee, A. Demchenko, M. Bandara, 2017 .

Investigation of the H-bond-mediated aglycone delivery reaction in application to the synthesis of β-glucosides.

J. P. Yasomanee, A. Demchenko, M. Mannino, 2018, Carbohydrate research.

Picoloyl-Protecting Group in Oligosaccharide Synthesis : Installation, H-Bond-Mediated Aglycone Delivery (HAD), and Selective Removal

J. P. Yasomanee, A. Demchenko, M. Mannino, 2017 .

Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot.

M. Bols, J. P. Yasomanee, A. Demchenko, 2017, Organic & biomolecular chemistry.

Synthesis of the Repeating Unit of Capsular Polysaccharide Staphylococcus aureus Type 5 To Study Chemical Activation and Conjugation of Native CP5.

J. P. Yasomanee, A. Demchenko, S. A. Kolodziej, 2016, Journal of Organic Chemistry.

Halobenzoyl groups in glycosylation: effect on stereoselectivity and reactivity of glycosyl donors

J. P. Yasomanee, A. Demchenko, Satsawat Visansirikul, 2015, Russian Chemical Bulletin.

A Concise Synthesis of the Repeating Unit of Capsular Polysaccharide Staphylococcus aureus Type 8.

J. P. Yasomanee, M. Kamat, A. Demchenko, 2015, Organic letters.