A Domino Michael/Dieckmann Process as an Entry to alpha-(Hydroxymethyl)glutamic Acid

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

    Universidad de La Rioja

    Logroño, España

    GRID grid.119021.a

  2. 2 University of California Los Angeles
    info

    University of California Los Angeles

    Los Ángeles, Estados Unidos

    GRID grid.19006.3e

Journal:
Journal of Organic Chemistry

ISSN: 0022-3263

Year of publication: 2011

Volume: 76

Issue: 17

Pages: 6990-6996

Type: Article

Export: RIS
DOI: 10.1021/jo201067n SCOPUS: 2-s2.0-80052154759 WoS: 000294242900002 GOOGLE SCHOLAR

Metrics

Cited by

  • Scopus Cited by: 8 (12-06-2021)

Journal Citation Reports

  • Year 2011
  • Journal Impact Factor: 4.45
  • Best Quartile: Q1
  • Area: CHEMISTRY, ORGANIC Quartile: Q1 Rank in area: 9/56 (Ranking edition: SCIE)

SCImago Journal Rank

  • Year 2011
  • SJR Journal Impact: 2.265
  • Best Quartile: Q1
  • Area: Organic Chemistry Quartile: Q1 Rank in area: 13/182

CiteScore

  • Year 2011
  • CiteScore of the Journal : 7.7
  • Area: Organic Chemistry Percentile: 92
  • Area: Medicine (all) Percentile: 89

Abstract

A domino process that involves a Michael-type addition followed by a Dieckmann reaction mediated by the participation of the cyclic carbamate group is the key step in the synthesis of both enantiomers of α-(hydroxymethyl) glutamic acid (HMG). © 2011 American C emical Society.