In the course of our work to prepare inhibitors of the enzyme dihydrofolate reductase, we desired to prepare sulfone analogues of some similar sulfides [1, 2].[...
© 2020 Mujahid Abas et al. A series of sulfonamide-bearing azaheterocyclic Schiff base derivatives 3...
This thesis documents the development of novel methodologies for access to sulfur-containing compoun...
Copyright © 2015 Park-media, Ltd. This is an open access article distributed under the Creative Comm...
In the course of our work to prepare inhibitors of the enzyme dihydrofolate reductase, we desired to...
In the course of our work to prepare inhibitors of the enzyme dihydrofolate reductase, we desired to...
In the course of our work to prepare inhibitors of the enzyme dihydrofolate reductase, we desired to...
In the folate biosynthetic pathway, sulfa drugs (sulfonamides and sulfones) compete with the natural...
This thesis focuses on the design and syntheses of the sulfonium-ion analogues of australine, lentig...
The C(sp2)-aryl sulfonate functional group is widely found in bioactive scaffolds but can often only...
Antibiotic resistance is one of the greatest public health challenges of our time. There is an urgen...
A simple synthesis of sulfonamides 4–22 as novel histone deacetylase (HDAC) inhibitors is described....
A palladium-catalysed aminosulfonylation process is used as the key-step in a one-pot, three-compone...
Sulfa drugs are well known blockers of folate synthesis, acting as competitive inhibitors of p-amino...
Inhibitors of sulfatase-2 are putative anticancer agents, but the discovery of potent small molecule...
A Schiff base (azomethine) is named after its inventor, Hugo Schiff and it is a functional group tha...
© 2020 Mujahid Abas et al. A series of sulfonamide-bearing azaheterocyclic Schiff base derivatives 3...
This thesis documents the development of novel methodologies for access to sulfur-containing compoun...
Copyright © 2015 Park-media, Ltd. This is an open access article distributed under the Creative Comm...
In the course of our work to prepare inhibitors of the enzyme dihydrofolate reductase, we desired to...
In the course of our work to prepare inhibitors of the enzyme dihydrofolate reductase, we desired to...
In the course of our work to prepare inhibitors of the enzyme dihydrofolate reductase, we desired to...
In the folate biosynthetic pathway, sulfa drugs (sulfonamides and sulfones) compete with the natural...
This thesis focuses on the design and syntheses of the sulfonium-ion analogues of australine, lentig...
The C(sp2)-aryl sulfonate functional group is widely found in bioactive scaffolds but can often only...
Antibiotic resistance is one of the greatest public health challenges of our time. There is an urgen...
A simple synthesis of sulfonamides 4–22 as novel histone deacetylase (HDAC) inhibitors is described....
A palladium-catalysed aminosulfonylation process is used as the key-step in a one-pot, three-compone...
Sulfa drugs are well known blockers of folate synthesis, acting as competitive inhibitors of p-amino...
Inhibitors of sulfatase-2 are putative anticancer agents, but the discovery of potent small molecule...
A Schiff base (azomethine) is named after its inventor, Hugo Schiff and it is a functional group tha...
© 2020 Mujahid Abas et al. A series of sulfonamide-bearing azaheterocyclic Schiff base derivatives 3...
This thesis documents the development of novel methodologies for access to sulfur-containing compoun...
Copyright © 2015 Park-media, Ltd. This is an open access article distributed under the Creative Comm...