Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence-Reference-Cited by-同舟云学术

Divergent synthesis of multi-substituted phenanthrenes via an internal redox reaction/ring expansion sequence

Published:2024 Issue:28 Volume:60 Page:3822-3825
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Koyama Ryosei¹,Anada Masahiro²³^ORCID,Sueki Shunsuke²³^ORCID,Makino Kosho²³,Kojima Tatsuhiro⁴^ORCID,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

2. Faculty of Pharmacy, Musashino University, Nishitokyo, Tokyo 202-8585, Japan

3. Research Institute of Pharmaceutical Sciences, Musashino University, Nishitokyo, Tokyo 202-8585, Japan

4. Department of Applied Chemistry, Kobe City College of Technology (KCCT), 8-3 Gakuen-Higashimachi, Nishi-ku, Kobe, 651-2194, Japan

Abstract

Divergent synthesis of multi-substituted phenanthrenes based on an internal redox reaction/ring expansion sequence was achieved.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC00797B

Reference62 articles.

1. Functionalization of Organic Molecules by Transition-Metal-Catalyzed C(sp3)H Activation

2. Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

3. C–H Functionalization in organic synthesis

4. Innate and Guided C–H Functionalization Logic

5. Catalytic asymmetric α-C(sp3)–H functionalization of amines

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