A Biomimetic Approach to Lanthionines

  1. Aydillo, C. 1
  2. Avenoza, A. 1
  3. Busto, J.H. 1
  4. Jiménez-Osés, G. 12
  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:
Organic Letters

ISSN: 1523-7060

Year of publication: 2012

Volume: 14

Issue: 1

Pages: 334-337

Type: Article

Export: RIS
DOI: 10.1021/ol203068s SCOPUS: 2-s2.0-84855499525 WoS: 000298828500086 GOOGLE SCHOLAR

Metrics

Cited by

  • Scopus Cited by: 18 (12-06-2021)

Journal Citation Reports

  • Year 2012
  • Journal Impact Factor: 6.142
  • Best Quartile: Q1
  • Area: CHEMISTRY, ORGANIC Quartile: Q1 Rank in area: 6/57 (Ranking edition: SCIE)

SCImago Journal Rank

  • Year 2012
  • SJR Journal Impact: 3.338
  • Best Quartile: Q1
  • Area: Biochemistry Quartile: Q1 Rank in area: 23/407
  • Area: Organic Chemistry Quartile: Q1 Rank in area: 5/185
  • Area: Physical and Theoretical Chemistry Quartile: Q1 Rank in area: 6/164

CiteScore

  • Year 2012
  • CiteScore of the Journal : 9.8
  • Area: Organic Chemistry Percentile: 97
  • Area: Biochemistry Percentile: 94
  • Area: Physical and Theoretical Chemistry Percentile: 94
  • Area: Medicine (all) Percentile: 93

Abstract

The asymmetric sulfa-Michael additions of appropriately protected l- and d-cysteine derivatives to new chiral dehydroamino acid derivatives have been developed as key steps in the synthesis of biologically important cysteine derivatives, such as lanthionine (Lan) and β-methyllanthionine (MeLan), which are unusual bis-α-amino acids found in the emerging lantibiotics such as nisin. © 2011 American Chemical Society.