| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5216455 | Tetrahedron | 2014 | 5 Pages | 
Abstract
												Starting with commercial and inexpensive reagents, a high-yielding chemical process carried out in [b-3C-im][NTf2] ionic liquid was achieved to afford the synthesis of batracylin and its N-sulfonamido analogues. Among all compounds synthesized, compounds 1, 11, and 14 exhibit potent inhibitory activity against human topoisomerase 1 (hTop1).
Graphical abstractDownload full-size imageStarting with commercial and inexpensive reagents, a high-yielding chemical process carried out in [b-3C-im][NTf2] ionic liquid was achieved to afford the synthesis of batracylin and its N-sulfonamido analogues. Among all compounds synthesized, compounds 1, 11, and 14 exhibit potent inhibitory activity against human topoisomerase 1 (hTop1).
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											Authors
												Ming-Chung Tseng, Peng-Yeh Lai, Lin Shi, Hsin-Yi Li, Min-Jen Tseng, Yen-Ho Chu, 
											![First Page Preview: Synthesis of batracylin and its N-sulfonamido analogues in [b-3C-im][NTf2] ionic liquid Synthesis of batracylin and its N-sulfonamido analogues in [b-3C-im][NTf2] ionic liquid](/preview/png/5216455.png)