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Original Articles

Diastereo and Enantioselective Synthesis of 1,2-Diols Promoted by Electrophilic Selenium Reagents

, , , , &
Pages 956-960 | Published online: 29 Oct 2008

REFERENCES AND NOTES

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  • Tiecco , M. , Testaferri , L. , Santi , C. , Tomassini , C. , Santoro , S. , Marini , F. , Bagnoli , L. , Temperini , A. and Costantino , F. 2006 . Eur. J. Org. Chem , : 4867
  • Tiecco , M. , Testaferri , L. , Santi , C. , Tomassini , C. , Bonini , R. , Marini , F. , Bagnoli , L. and Temperini , A. 2004 . Org. Lett. , 6 : 4751
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  • Tiecco , M. , Testaferri , L. , Tingoli , M. , Bagnoli , L. and Santi , C. 1993 . J. Chem. Soc. Chem. Commun. , : 637
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  • 1H and 13C NMR spectra were recorded at 400 and 100.62 MHz, respectively, on a Bruker Avance-DRX 400 instrument. Unless otherwise specified, CDCl3 was used as the solvent and TMS as internal standard. GC-MS analyses were carried out with an HP-6890 gas chromatograph (dimethyl silicone column, 12.5 m) equipped with an HP-5973 mass-selective detector. IR spectra were recorded on a JASCO FT/IR-410 spectrophotometer using a multiple reflection horizontal ATR (HATR) accessory. Optical rotations were measured with a JASCO DIP-1000 digital polarimeter
  • Jonsson , S. , Adolfsson , H. and Backvall , J.-E. 2001 . Org. Lett. , 3 : 3463

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