Planar Chirality Directs Enantiospecific Diastereoselectivity in Isocyanide-Based Multicomponent Reactions.

Kapsalis M, Fragkiadakis M, Konstantaras I, Froudas KG, Stergiannakos T, Sun R, Benedetti E, Neochoritis CG

Open source

DOI: 10.1021/acsorginorgau.6c00034
Published: 2026 Aug 5
Container: ACS organic & inorganic Au
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1021/acsorginorgau.6c00034,
  title = {Planar Chirality Directs Enantiospecific Diastereoselectivity in Isocyanide-Based Multicomponent Reactions.},
  author = {Kapsalis M and Fragkiadakis M and Konstantaras I and Froudas KG and Stergiannakos T and Sun R and Benedetti E and Neochoritis CG},
  year = {2026},
  journal = {ACS organic \& inorganic Au},
  doi = {10.1021/acsorginorgau.6c00034},
  url = {https://doi.org/10.1021/acsorginorgau.6c00034}
}

RIS

TY  - JOUR
TI  - Planar Chirality Directs Enantiospecific Diastereoselectivity in Isocyanide-Based Multicomponent Reactions.
AU  - Kapsalis M
AU  - Fragkiadakis M
AU  - Konstantaras I
AU  - Froudas KG
AU  - Stergiannakos T
AU  - Sun R
AU  - Benedetti E
AU  - Neochoritis CG
PY  - 2026
JO  - ACS organic & inorganic Au
DO  - 10.1021/acsorginorgau.6c00034
UR  - https://doi.org/10.1021/acsorginorgau.6c00034
ER  -

APA

M, K., M, F., I, K., KG, F., T, S., R, S., E, B., & CG, N. (2026). Planar Chirality Directs Enantiospecific Diastereoselectivity in Isocyanide-Based Multicomponent Reactions.. ACS organic & inorganic Au. https://doi.org/10.1021/acsorginorgau.6c00034

Source records

pubmed · retrieved 2026-09-26T11:43:44.998Z
europe-pmc · retrieved 2026-09-26T11:43:44.990Z
doaj · retrieved 2026-09-26T11:43:44.981Z
hal · retrieved 2026-09-26T11:43:45.026Z