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Palladium-Catalyzed Regio- and Enantioselective Synthesis of Allylic Amines Featuring Tetrasubstituted Tertiary Carbons

Open access
Cai, Aijie, Guo, Wusheng, Martínez-Rodríguez, Luis, Kleij, Arjan W.·2016·Journal of the American Chemical Society

Abstract

The first asymmetric synthesis of α,α-disubstituted allylic N-arylamines based on a palladium-catalyzed allylic amination has been developed. The protocol uses highly modular vinyl cyclic carbonates and unactivated aromatic amine nucleophiles as substrates. The catalytic process features minimal waste production, ample scope in reaction partners, high asymmetric induction up to 97% ee, and operational simplicity.

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Metadata

Authors
Cai, A., Guo, W., Martínez-Rodríguez, L., & Kleij, A. W.
Venue
Journal of the American Chemical Society
Published
2016-10-21
Volume
138
Issue
43
Pages
14194-14197
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2533049456
Cited by
207
References
0
FWCI
11.29
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Palladium-Catalyzed Regio- and Enantioselective Synthesis of Allylic Amines Featuring Tetrasubstituted Tertiary Carbons. https://app.cochat.ai/papers/10.1021/jacs.6b08841
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Cai, A., Guo, W., Martínez-Rodríguez, L., & Kleij, A. W. (2016). Palladium-Catalyzed Regio- and Enantioselective Synthesis of Allylic Amines Featuring Tetrasubstituted Tertiary Carbons. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.6b08841

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.