Synlett 2004(9): 1619-1621  
DOI: 10.1055/s-2004-829080
LETTER
© Georg Thieme Verlag Stuttgart · New York

Vaulted Biaryls: Efficient Ligands for the Aluminum-Catalyzed Asymmetric Baeyer-Villiger Reaction

Carsten Bolm*a, Jean-Cédric Frisona, Yu Zhangb, William D. Wulffb
a Institut für Organische Chemie der RWTH Aachen, Professor Pirlet-Str. 1, 52056 Aachen, Germany
Fax: +49(241)8092391; e-Mail: Carsten.Bolm@oc.RWTH-Aachen.de;
b Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, USA
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Publikationsverlauf

Received 20 March 2004
Publikationsdatum:
29. Juni 2004 (online)

Abstract

Vaulted biaryls (VANOL and VAPOL) have been applied in the aluminum-catalyzed asymmetric Baeyer-Villiger ­reaction of prochiral 3-substituted cyclobutanones. Optically active γ-butyrolactones are obtained in high yields with enantioselectivities of up to 84% ee.

    References

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  • 1b Krow GR. In Comprehensive Organic Chemistry   Vol. 7:  Trost BM. Pergamon Press; Oxford: 1991.  p.671 
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  • Reviews:
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  • 3b Bolm C. In Peroxide Chemistry   Adam W. Wiley-VCH; Weinheim: 2000.  p.494 
  • 3c Bolm C. Beckmann O. In Comprehensive Asymmetric Catalysis   Vol. 2:  Jacobsen EN. Pfaltz A. Yamamoto H. Springer-Verlag; Stuttgart: 1999.  p.803 
  • 3d Bolm C. Med. Res. Rev.  1999,  19:  348 
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  • For other recent examples of metal-catalyzed asymmetric Baeyer-Villiger reactions focusing on the conversions of cyclobutanones, see:
  • 13a Uchida T. Katsuki T. Ito K. Akashi S. Ishii A. Kuroda T. Helv. Chim. Acta  2002,  85:  3078 
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  • 14 To the best of our knowledge there is only a single report with a higher ee. Katsuki et al. found a zirconium catalyst bearing a complex salen ligand to give 87% ee in the conversion of 4 to 5. See: Watanabe A. Uchida T. Ito K. Katsuki T. Tetrahedron Lett.  2002,  43:  4481 
10

After 72 h at -40 °C the reaction was quenched to give the lactone with 84% ee in 40% yield.

11

Experimental Procedure for the Al-Catalyzed Asymmetric Baeyer-Villiger Reaction.
To a solution of (R)-VANOL (26.4 mg, 0.06 mmol) in toluene (2.5 mL) was added dropwise Me2AlCl (0.06 mmol, 60 µL, 1 M solution in hexanes) at r.t. The mixture was stirred for 30 min and then cooled at -30 °C. After 15 min at this temperature, a solution of the ketone (0.3 mmol) in toluene (0.5 mL) was added. Stirring was continued for 15 min, cumene hydroperoxide (technical grade 80%, 1.2 equiv, 75 µL) was then added in one portion. Subsequently, the reaction mixture was stirred at -30 °C until full conversion of the ketone (as monitored by GC). The solvent was then evaporated, and the crude product absorbed onto silica gel. Extraction with Et2O afforded the crude product, which was analyzed by GC or HPLC using chiral columns (for details of the enantiomeric ratio determinations and assignments of absolute configurations, see ref. 4 and references therein).

12

Slightly better results can be obtained for benzyl-substituted substrates when 50 mol% of the BINOL/Me2AlCl catalyst system are applied (comp. ref. 4a). Thus, conversions of 6c and 6d give lactones with 73% and 58% ee, respectively.