Rhodium-Catalyzed Intermolecular [4+2] Cycloaddition of Unactivated Substrates
โ Scribed by Masahiro Murakami; Minoru Ubukata; Kenichiro Itami; Yoshihiko Ito
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 102 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0044-8249
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โฆ Synopsis
No electron-withdrawing or electron-releasing substituents are necessary for the substrates in the rhodium-catalyzed [4+2] cycloaddition reaction between a vinylallene and an ordinary alkyne under mild conditions [Eq. (1)]. The use of the strongly electron-accepting P[OCH(CF ) ] ligand affords the optimal rhodium catalyst. cod = 1,5-cyclooctadiene.
๐ SIMILAR VOLUMES
Directed Intermolecular (4 + 2) Cycloaddition of Unactivated 1,3-Diene Substrates with High Regio-and Stereoselectivities. -Pd(0)-catalyzed cycloaddition of vinylallenes with ordinary 1,3-dienes leads to cyclohexene derivatives. High regio-and stereoselectivities are achieved under mild conditions
## Abstract For Abstract see ChemInform Abstract in Full Text.