RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2015; 47(15): 2217-2222
DOI: 10.1055/s-0034-1379928
DOI: 10.1055/s-0034-1379928
special topic
Asymmetric Conjugate Addition of Alkylzirconocenes to Cyclopent-4-ene-1,3-dione Monoacetals
Weitere Informationen
Publikationsverlauf
Received: 27. März 2015
Accepted after revision: 06. Mai 2015
Publikationsdatum:
01. Juli 2015 (online)

Abstract
Copper-catalyzed asymmetric conjugate additions are powerful reactions that allow the formation of single-enantiomer building blocks in a few steps. However, highly enantioselective conjugate addition to five-membered-ring substrates is more challenging and is often neglected. Here, we report catalytic asymmetric 1,4-addition of alkylzirconocenes, formed in situ from readily available alkenes, to cyclopent-4-ene-1,3-dione monoacetals. Good to high enantioselectivities are observed and the procedure tolerates various functional groups.
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1379928.
- Supporting Information
-
References
- 1a Harutyunyan SR, den Hartog T, Geurts K, Minnaard AJ, Feringa BL. Chem. Rev. 2008; 108: 2824
- 1b Copper-Catalyzed Asymmetric Synthesis . Alexakis A, Krause N, Woodward S. Wiley-VCH; Weinheim: 2014
- 1c Krause N, Hoffmann-Röder A. Synthesis 2001; 171
- 1d Hayashi T, Yamasaki K. Chem. Rev. 2003; 103: 2829
- 1e Alexakis A, Bäckvall JE, Krause N, Pàmies O, Diéguez M. Chem. Rev. 2008; 108: 2796
- 1f Maksymowicz RA, Bissette AJ, Fletcher SP. Chem. Eur. J. 2015; 21: 5668
- 2a Feringa BL. Acc. Chem. Res. 2000; 33: 346
- 2b Krause N. Angew. Chem. Int. Ed. 1998; 37: 283
- 2c Kanai M, Nakagawa Y, Tomioka K. Tetrahedron 1999; 55: 3843
- 3 Degrado SJ, Mizutani H, Hoveyda AH. J. Am. Chem. Soc. 2001; 123: 755
- 4a Brown MK, Hoveyda AH. J. Am. Chem. Soc. 2008; 130: 12904
- 4b Jansen DJ, Shenvi RA. J. Am. Chem. Soc. 2013; 135: 1209
- 4c Sunazuka T, Hirose T, Shirahata T, Harigaya Y, Hayashi M, Komiyama K, Ōmura S, Smith AB. J. Am. Chem. Soc. 2000; 122: 2122
- 4d Arnold LA, Naasz R, Minnaard AJ, Feringa BL. J. Am. Chem. Soc. 2001; 123: 5841
- 5a Maksymowicz RM, Roth PM. C, Fletcher SP. Nat. Chem. 2012; 4: 649
- 5b Sidera M, Roth PM. C, Maksymowicz RM, Fletcher SP. Angew. Chem. Int. Ed. 2013; 52: 7995
- 5c Maksymowicz RM, Roth PM. C, Thompson AL, Fletcher SP. Chem. Commun. 2013; 49: 4211
- 5d Maksymowicz RM, Sidera M, Roth PM. C, Fletcher SP. Synthesis 2013; 45: 2662
- 5e Roth PM. C, Sidera M, Maksymowicz RM, Fletcher SP. Nat. Protoc. 2014; 9: 104
- 5f Maciver EE, Maksymowicz RM, Wilkinson N, Roth PM. C, Fletcher SP. Org. Lett. 2014; 16: 3288
- 5g Roth PM. C, Fletcher SP. Org. Lett. 2015; 17: 912
- 5h You H, Rideau E, Sidera M, Fletcher SP. Nature 2015; 517: 351
- 5i Mola L, Sidera M, Fletcher SP. Aust. J. Chem. 2015; 68: 401
- 5j Sidera M, Fletcher SP. Chem. Commun. 2015; 51: 5044
- 6 Arnold LA, Naasz R, Minnaard AJ, Feringa BL. J. Org. Chem. 2002; 67: 7244