Abstract
The 8-chlorobicyclo[3.2.1]oct-6-ene 3 has been prepared by a [3+2] cycloaddition route, and converted to the bicyclic alpha -methylene ketones 6 and 8-12. some of which showed cytotoxic properties. (C) 2001 Elsevier Science Ltd. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 2729-2731 |
| Number of pages | 3 |
| Journal | Tetrahedron Letters |
| Volume | 42 |
| Publication status | Published - 2 Apr 2001 |
Keywords
- [3+2] cycloaddition
- Hg(II) mediated hydrolysis
- alkynyl and vinyl sulphide
- bicyclo[3.2.1]octane alpha-methylene ketones
- cytotoxicity
- TERRECYCLIC ACID-A
- ASPERGILLUS-TERREUS
- PROSTANOIDS
Fingerprint
Dive into the research topics of 'Synthesis and cytotoxic properties of a series of bicyclo[3.2.1]octane alpha-methylene ketones'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver