We have undertaken a synthesis of this substance as part of a broader program in the area of biologically active macrocyclic natural products. One attractive approach to the synthesis of maytansine involves the introduction of chiraltty at carbons 3, 4, 5, 10, and 9 after formation of the macro ring
Concise route to the key intermediate for divergent synthesis of C7-substituted fluoroquinolone derivatives
โ Scribed by Xin Zhang; Feng Mu; Bobby Robinson; Pengfei Wang
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 211 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A concise route to ethyl 7-bromo-1-cyclopropyl-6,8-difluoro-4-quinolone-3-carboxylate has been developed. This compound is a key intermediate for divergent synthesis of various C7-substituted fluoroquinolones, a group of potent topoisomerase II inhibitors with promising clinical applications.
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