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Rhodium-Catalyzed Intermolecular [4+2] Cycloaddition of Unactivated Substrates

โœ 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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โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Directed Intermolec
โœ M. MURAKAMI; K. ITAMI; Y. ITO ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 31 KB ๐Ÿ‘ 1 views

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