Organocatalytic Asymmetric Formal Aza-[3 + 2] Cycloaddition via Domino Michael/Acetalization: Stereoselective Access to 3,4-cis-Disubstituted Pyrrolidines and Pot-Economical Total Syntheses of (-)-Kainic Acid and (-)-Domoic Acid.
- DOI
- 10.1021/jacsau.6c00915
- Published
- 2026 Aug 24
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- JACS Au
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1021/jacsau.6c00915,
title = {Organocatalytic Asymmetric Formal Aza-[3 + 2] Cycloaddition via Domino Michael/Acetalization: Stereoselective Access to 3,4-cis-Disubstituted Pyrrolidines and Pot-Economical Total Syntheses of (-)-Kainic Acid and (-)-Domoic Acid.},
author = {Hatano Y and Odaira H and Tachibana T and Hayashi Y},
year = {2026},
journal = {JACS Au},
doi = {10.1021/jacsau.6c00915},
url = {https://doi.org/10.1021/jacsau.6c00915}
}RIS
TY - JOUR TI - Organocatalytic Asymmetric Formal Aza-[3 + 2] Cycloaddition via Domino Michael/Acetalization: Stereoselective Access to 3,4-cis-Disubstituted Pyrrolidines and Pot-Economical Total Syntheses of (-)-Kainic Acid and (-)-Domoic Acid. AU - Hatano Y AU - Odaira H AU - Tachibana T AU - Hayashi Y PY - 2026 JO - JACS Au DO - 10.1021/jacsau.6c00915 UR - https://doi.org/10.1021/jacsau.6c00915 ER -
APA
Y, H., H, O., T, T., & Y, H. (2026). Organocatalytic Asymmetric Formal Aza-[3 + 2] Cycloaddition via Domino Michael/Acetalization: Stereoselective Access to 3,4-cis-Disubstituted Pyrrolidines and Pot-Economical Total Syntheses of (-)-Kainic Acid and (-)-Domoic Acid.. JACS Au. https://doi.org/10.1021/jacsau.6c00915
Source records
- pubmed · retrieved 2026-09-26T15:16:07.961Z