The DOI matches its Crossref record.
Heck−Suzuki−Miyaura Domino Reactions Involving Ynamides. An Efficient Access to 3-(Arylmethylene)isoindolinones
Abstract
[reaction: see text] Substituted 3-(arylmethylene)isoindolin-1-ones can be efficiently synthesized in a stereoselective manner from various ynamides and boronic acids by palladium-catalyzed Heck-Suzuki-Miyaura domino reactions.
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Citations
Cited by
Ynamides: A Modern Functional Group for the New Millennium
DeKorver, K. A., Li, H., Lohse, A. G., Hayashi, R., Lu, Z., Zhang, Y., & Hsung, R. P. (2010) · Chemical Reviews · doi:10.1021/cr100003s · Cited by 886
Ynamides: Versatile Tools in Organic Synthesis
Evano, G., Coste, A., & Jouvin, K. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200905817 · Cited by 812
Metadata
- Authors
- Couty, S., Liégault, B., Meyer, C., & Cossy, J.
- Venue
- Organic Letters
- Publisher
- American Chemical Society (ACS)
- Published
- 2004-06-24
- Volume
- 6
- Issue
- 15
- Pages
- 2511-2514
- ISSN
- 1523-7052 (ISSN-L)
- 1523-7060
- OpenAlex
- W2069264952
- Cited by
- 164
- References
- 0
- FWCI
- 6.36
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Heck−Suzuki−Miyaura Domino Reactions Involving Ynamides. An Efficient Access to 3-(Arylmethylene)isoindolinones. https://app.cochat.ai/papers/10.1021/ol049302m
- The paper
- Couty, S., Liégault, B., Meyer, C., & Cossy, J. (2004). Heck−Suzuki−Miyaura Domino Reactions Involving Ynamides. An Efficient Access to 3-(Arylmethylene)isoindolinones. Organic Letters. https://doi.org/10.1021/ol049302m
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.