Regioselective Diels-Alder reactions. A synthesis of the left-hand portion of CC-1065
โ Scribed by Kraus, George A.; Yue, Stephen; Sy, James
- Book ID
- 126791653
- Publisher
- American Chemical Society
- Year
- 1985
- Tongue
- English
- Weight
- 265 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract The 2,5โdimethylideneโ3,6โbis[(__Z__)โ(2โnitrophenyl)sulfenylmethylidene]โ7โoxabicyclo[2.2.1]heptane (**13**) can be used to generate polyfunctional and multicyclic molecules with high regioโ and stereoselectivity __via__ two successive __Diels__โ__Alder__ additions using two different
Total Synthesis of Maturinone Through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione. -Using a known directing effect of a bromine atom located on the double bond of a quinone such as (III) in a Diels-Alder reaction maturinone ( VI) is synthesized in an efficient and regiosel