α-Iminol Rearrangement Triggered by Pd-Catalyzed C–H Addition to Nitriles Sequences: Synthesis of Functionalized α-Amino Cyclopentanones-Reference-Cited by-同舟云学术

α-Iminol Rearrangement Triggered by Pd-Catalyzed C–H Addition to Nitriles Sequences: Synthesis of Functionalized α-Amino Cyclopentanones

Published:2021-01-26 Issue:3 Volume:23 Page:1021-1025
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Cheng Na¹,Cui Shu-Qiang¹,Ma Qian-Qian¹,Wei Zhong-Lin¹,Liao Wei-Wei¹²^ORCID

Affiliation:

1. Department of Organic Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P.R. China

2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, P.R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c04214

Reference46 articles.

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2. Über Bestandteile der Nebennierenrinde und verwandte Stoffe. 57. Mitteilung. 17-Oxy-20-keto-steroide und der Mechanismus ihrer Umlagerung zu Polyhydrochrysen-Derivaten

3. Molecular rearrangements yielding Δ2-pyrazolin-5-ones: acyloin rearrangement

4. Baseninduzierte Acyloin‐ Umlagerung sterisch gehinderter p ‐Chinole

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