Asymmetric synthesis of 1-aryl and 1,3-diarylcyclopentenes by the Heck reaction of 1-sulfinylcyclopentenes with iodoarenes
✍ Scribed by Juan Carlos de la Rosa; Nuria Dı́az; Juan C Carretero
- Book ID
- 104210341
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 178 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The asymmetric synthesis of 1-aryl and 1,3-diarylcyclopentenes by Heck reaction of (R)-1-[o-(N,Ndimethylamino)phenylsufinyl]cyclopentene with iodoarenes is described.
📜 SIMILAR VOLUMES
The first examples of the synthesis of 1,3-dienyl sulfoxides by Heck reactions are described. Both racemic and enantiomerically pure exocyclic 1-p-tolylsulfinyl-1,3-dienes 1 are readily prepared by the intramolecular Heck reaction of their corresponding vinyl iodides in the presence of Pd(OAc) 2 as
New, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic carbene precursors were synthesized and characterized. These salts, combined with palladium acetate, provided active catalysts for Heck and Suzuki cross-coupling of aryl chlorides and bromides under mild conditions.
## Dedicated to Professor Dr. Fritz Sauter on the occasion of his 75 th birthday 1-Acetyl-and 1-propionyl-2-pyrazolines 11-27 have been synthesized by the reaction of (3coumarinyl)chalcones 1-10 with hydrazine in hot acetic acid or propionic acid. While 5-aryl-3-(3coumarinyl)-1-phenyl-2-pyrazoline