The photoaddition of alkenes to 2,2-dimethyl-3(2H)-furanone affords products which can be efficiently elaborated to cyclohexenones by two different methods. During the past several years we have been exploring the utility of acyclic a-formy ketones, particularly formyl acetone, as partners in the ph
Face selectivity in the [2+2] photoannelation of chiral 3(2h)-furanones with alkenes
β Scribed by S.W Baldwin; T.J Mazzuckelli; Paul M Gross
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 281 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The photocycloadditions of a series of chiral 3(2H)-l'uranones with alkenes show facial selectivilies which parallel the steric bulk of the furanone substituents.
Selectivities approaching 50: 1 are observed in some instances.
π SIMILAR VOLUMES
## Abstract 3,4βDichloroβ2(5__H__)βfuranone, which has been prepared efficiently from mucochloric acid, has been transformed selectively into 4βarylβ3βchloroβ2(5__H__)βfuranones either by Suzukiβ or Stilleβtype reactions. These monochloro derivatives have been used as precursors either to (__Z__)β4
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