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Rongze Kuang

Wichita State University

33

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A ONE-STEP PROTOCOL FOR THE N-CHLOROMETHYLATION OF HETEROCYCLIC IMIDES

2001 Synthetic Communications
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Inhibition of serine proteases by functionalized sulfonamides coupled to the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold.

2001 Bioorganic & Medicinal Chemistry
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Inhibition of serine proteases by functionalized sulfonamides coupled to the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold

2001 Bioorganic & Medicinal Chemistry
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1,2,5-Thiadiazolidin-3-one 1,1 dioxide: a powerful scaffold for probing the S' subsites of (chymo)trypsin-like serine proteases

2001 Archives of Biochemistry and Biophysics
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Utilization of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold in the design of potent inhibitors of serine proteases: SAR studies using carboxylates

2000 Bioorganic & Medicinal Chemistry
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Use of the 1,2,5-Thiadiazolidin-3-one 1,1 Dioxide and Isothiazolidin-3-one 1,1 Dioxide Scaffolds in the Design of Potent Inhibitors of Serine Proteinases.

1998 ChemInform
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Potent and specific inhibition of human leukocyte elastase, cathepsin G and proteinase 3 by sulfone derivatives employing the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold

1998
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Potent and specific inhibition of human leukocyte elastase, cathepsin G and proteinase 3 by sulfone derivatives employing the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold.

1998 Bioorganic & Medicinal Chemistry
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Use of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide and isothiazolidin-3-one 1,1 dioxide scaffolds in the design of potent inhibitors of serine proteinases

1998 Bioorganic & Medicinal Chemistry Letters
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Use of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide and isothiazolidin-3-one 1,1 dioxide scaffolds in the design of potent inhibitors of serine proteinases

1998
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