Pyridine-mediated tandem Knoevenagel condensation-decarboxylation: Chemoselectivity, mechanistic rationale, and discovery of a novel Lead(II) fumarate coordination polymer.

Köntös Z, Bartek M

DOI: 10.1177/00368504261477972
Published: 2026 Jul-Sep
Container: Science progress
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1177/00368504261477972,
  title = {Pyridine-mediated tandem Knoevenagel condensation-decarboxylation: Chemoselectivity, mechanistic rationale, and discovery of a novel Lead(II) fumarate coordination polymer.},
  author = {Köntös Z and Bartek M},
  year = {2026},
  journal = {Science progress},
  doi = {10.1177/00368504261477972},
  url = {https://doi.org/10.1177/00368504261477972}
}

RIS

TY  - JOUR
TI  - Pyridine-mediated tandem Knoevenagel condensation-decarboxylation: Chemoselectivity, mechanistic rationale, and discovery of a novel Lead(II) fumarate coordination polymer.
AU  - Köntös Z
AU  - Bartek M
PY  - 2026
JO  - Science progress
DO  - 10.1177/00368504261477972
UR  - https://doi.org/10.1177/00368504261477972
ER  -

APA

Z, K., & M, B. (2026). Pyridine-mediated tandem Knoevenagel condensation-decarboxylation: Chemoselectivity, mechanistic rationale, and discovery of a novel Lead(II) fumarate coordination polymer.. Science progress. https://doi.org/10.1177/00368504261477972

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pubmed · retrieved 2026-09-25T12:13:14.114Z