A Convenient Enantioselective Synthesis of (S)-alfa-Trifluoromethylisoserine

  1. Avenoza, A. 1
  2. Busto, J.H. 1
  3. Jiménez-Osés, G. 1
  4. Peregrina, J.M. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Aldizkaria:
Journal of Organic Chemistry

ISSN: 0022-3263

Argitalpen urtea: 2005

Alea: 70

Zenbakia: 14

Orrialdeak: 5721-5724

Mota: Artikulua

DOI: 10.1021/JO0505371 PMID: 15989359 SCOPUS: 2-s2.0-22144478679 WoS: WOS:000230355200046 GOOGLE SCHOLAR

Beste argitalpen batzuk: Journal of Organic Chemistry

Gordailu instituzionala: lock_openSarbide irekia Editor

Laburpena

This report describes two straightforward synthetic methodologies to obtain α-CF3-isoserine, a new α,α-disubstituted β-amino acid, from α-(trifluoromethyl)acrylic acid. The routes involve the synthesis of five-membered cyclic sulfates (using sulfuryl chloride) or sulfamidates (using the Burgess reagent) from the corresponding chiral diols, which are obtained by a catalytic asymmetric dihydroxylation (AD) reaction. © 2005 American Chemical Society.