Abstract
The chemistry of squalene oxide (1) exemplifies that architectural complexity can be encoded in the structures of relatively simple, polyunsaturated molecules. When the concept of architectural self-construction is an integral part of the design of a chemical synthesis, powerful strategies can be uncovered. this article addresses studies which showed that polyunsaturated, 19-membered ring carbocycle contains all of the molecular information that is required to give the stereochemically complex polycyclic architecture of the cytotoxic natural product FR182877.
Original language | English (US) |
---|---|
Pages (from-to) | 3225-3228 |
Number of pages | 4 |
Journal | Bioorganic and Medicinal Chemistry |
Volume | 11 |
Issue number | 15 |
DOIs | |
State | Published - Jul 31 2003 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Drug Discovery
- Molecular Medicine
- Molecular Biology
- Biochemistry
- Clinical Biochemistry
- Pharmaceutical Science
- Organic Chemistry