New strategy for the synthesis of the taxane diterpenes: Formation of the BC-rings of taxol via a [5+2]-pyrylium ylide-alkene cyclization, ring expansion strategy
✍ Scribed by William Bauta; John Booth; Mary Ellen Bos; Mark DeLuca; Louis Diorazio; Timothy Donohoe; Nicholas Magnus; Philip Magnus; José Mendoza; Philip Pye; James Tarrant; Stephen Thom; Feroze Ujjainwalla
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 210 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A highly efficient strategy for the iterative synthesis of a trans-fused polytetrahydropyran ring system was developed. The new iterative method involves SmI2-induced reductive intramolecular cyclization of an aldehyde and a [~-alkoxy acrylate as the key step, producing a 2,3-trans-tetrahydropyran r
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v