Cyclic Iodine Reagents Enable Allylic Alcohols for Alkyl Boronate Addition/Rearrangement by Photoredox Catalysis-Reference-Cited by-同舟云学术

Cyclic Iodine Reagents Enable Allylic Alcohols for Alkyl Boronate Addition/Rearrangement by Photoredox Catalysis

Published:2018-10-26 Issue:12 Volume:36 Page:1209-1212
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Liu Mingshang¹²,Huang Hanchu¹,Chen Yiyun¹²

Affiliation:

1. State Key Laboratory of Bioorganic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences; 345 Lingling Road, Shanghai 200032 China

2. School of Physical Science and Technology, ShanghaiTech University; 100 Haike Road, Shanghai 201210 China

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cjoc.201800461/fullpdf

Reference68 articles.

1. The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters

2. Asymmetric Catalysis Special Feature Part I: Catalytic asymmetric synthesis of all-carbon quaternary stereocenters

3. Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis

4. Transposition of Allylic Alcohols into Carbonyl Compounds Mediated by Transition Metal Complexes

Cited by 34 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. Recent Progress in Synthetic Applications of Hypervalent Iodine(III) Reagents;Chemical Reviews;2024-09-13

2. Organohypervalent heterocycles;Chemical Society Reviews;2024

3. Photoinduced Pyridine N‐oxides Catalyzed Carbon Radical Generation from Alkylboronic Acids;ChemCatChem;2023-09-18

4. Visible‐Light‐Promoted Aliphatic C−H Chlorination and Bromination Using Haloform as the Halogen Donor and Azidobenziodoxole as the Mediator;Advanced Synthesis & Catalysis;2023-07-27

5. A Domino Radical Amidation/Semipinacol Approach to All‐Carbon Quaternary Centers Bearing an Aminomethyl Group;Chemistry – A European Journal;2023-07-24