Isothiourea-Catalyzed Enantioselective Functionalisation of Glycine Schiff Base Aryl Esters via 1,6- and 1,4-Additions.

Stockhammer L, Craik R, Monkowius U, Cordes DB, Smith AD, Waser M.

Open source

DOI: 10.1002/ceur.202300015
Published: 2023-05-03
Container: ChemistryEurope
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/ceur.202300015,
  title = {Isothiourea-Catalyzed Enantioselective Functionalisation of Glycine Schiff Base Aryl Esters via 1,6- and 1,4-Additions.},
  author = {Stockhammer L and  Craik R and  Monkowius U and  Cordes DB and  Smith AD and  Waser M.},
  year = {2023},
  journal = {ChemistryEurope},
  doi = {10.1002/ceur.202300015},
  url = {https://doi.org/10.1002/ceur.202300015}
}

RIS

TY  - JOUR
TI  - Isothiourea-Catalyzed Enantioselective Functionalisation of Glycine Schiff Base Aryl Esters via 1,6- and 1,4-Additions.
AU  - Stockhammer L
AU  -  Craik R
AU  -  Monkowius U
AU  -  Cordes DB
AU  -  Smith AD
AU  -  Waser M.
PY  - 2023
JO  - ChemistryEurope
DO  - 10.1002/ceur.202300015
UR  - https://doi.org/10.1002/ceur.202300015
ER  -

APA

L, S., R, C., U, M., DB, C., AD, S., & M., W. (2023). Isothiourea-Catalyzed Enantioselective Functionalisation of Glycine Schiff Base Aryl Esters via 1,6- and 1,4-Additions.. ChemistryEurope. https://doi.org/10.1002/ceur.202300015

Source records

europe-pmc · retrieved 2026-09-25T15:41:31.104Z
doaj · retrieved 2026-09-25T15:41:31.094Z