Silyl-Group Boosted Internal Redox Reaction: Hydride Shift from an Aliphatic Secondary Position for the Formation of Six- and Seven-Membered Carbocycles-Reference-Cited by-同舟云学术

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Silyl-Group Boosted Internal Redox Reaction: Hydride Shift from an Aliphatic Secondary Position for the Formation of Six- and Seven-Membered Carbocycles

Published:2024-02-21 Issue:8 Volume:26 Page:1662-1666
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Okawa Hiroto¹,Kawasaki-Takasuka Tomoko¹,Mori Keiji¹^ORCID

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Nakacho, Koganei, Tokyo 184-8588, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00140

Reference43 articles.

1. C–H Functionalization in organic synthesis

2. Innate and Guided C–H Functionalization Logic

3. Recent Advances in C–H Functionalization

4. Controllable Remote C−H Bond Functionalization by Visible-Light Photocatalysis

5. CH Bond Functionalization through Intramolecular Hydride Transfer

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of Polysubstituted Naphthalenes by a Hydride Shift Mediated C–H Bond Functionalization/Aromatization Sequence;Organic Letters;2024-02-28

2. Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters via an internal redox reaction/inverse electron-demand hetero-Diels–Alder reaction sequence;Chemical Communications;2024

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