Organic Letters 2007-08-02

Medium-sized carbocycles by a zirconocene-catalyzed tandem formal ring expansion-magnesation reaction of alkenyl-substituted cyclic enol ethers.

José Barluenga, Lucía Alvarez-Rodrigo, Félix Rodríguez, Francisco J Fañanás

Index: Org. Lett. 9(16) , 3081-4, (2007)

Full Text: HTML

Abstract

A new regio- and stereoselective zirconocene-catalyzed reaction for the synthesis of medium-sized rings is described. The global reaction supposes a formal ring expansion of a cyclic enol ether to give a functionalized carbocycle.


Related Compounds

  • Bis(cyclopentadien...

Related Articles:

Unusual temperature effects in propene polymerization using stereorigid zirconocene catalysts.

2003-02-15

[ChemPhysChem 6(9) , 1929-33, (2005)]

Enantioselective route from carbohydrates to cyclooctane polyols.

2005-02-03

[Org. Lett. 7(3) , 511-3, (2005)]

Functionalised cyclopentadienyl zirconium compounds as potential anticancer drugs.

2008-10-21

[Dalton Trans. (39) , 5293-5, (2008)]

Formal total synthesis of (+/-)-estrone and zirconocene-promoted cyclization of 2-fluoro-1,7-octadienes and ru-catalyzed ring closing metathesis.

2008-08-15

[J. Org. Chem. 73(16) , 6202-6, (2008)]

In pursuit of pestalotiopsin a via zirconocene-mediated ring contraction.

2006-05-25

[Org. Lett. 8(11) , 2429-31, (2006)]

More Articles...