Rh-Catalyzed Hydroheteroarylation of Styrenes: Access to Alkylated Heteroarenes with All-Carbon Quaternary Centers

Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom-economic rhodium and thiophenol co-catalyzed hydroheteroarylation of styrenes with heteroarenes is reported. Alkylated unprotected heteroarenes are accessed under low catalyst l...

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Published inEuropean journal of organic chemistry Vol. 26; no. 34
Main Authors Wang, Zhen, Wang, Yi-Xin, Yang, Xiao-Hui
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 06.09.2023
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Abstract Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom-economic rhodium and thiophenol co-catalyzed hydroheteroarylation of styrenes with heteroarenes is reported. Alkylated unprotected heteroarenes are accessed under low catalyst loading. This protocol provides straightforward access to indoles bearing an all-carbon quaternary center at the C3-position.
AbstractList Abstract Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom‐economic rhodium and thiophenol co‐catalyzed hydroheteroarylation of styrenes with heteroarenes is reported. Alkylated unprotected heteroarenes are accessed under low catalyst loading. This protocol provides straightforward access to indoles bearing an all‐carbon quaternary center at the C3‐position.
Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom‐economic rhodium and thiophenol co‐catalyzed hydroheteroarylation of styrenes with heteroarenes is reported. Alkylated unprotected heteroarenes are accessed under low catalyst loading. This protocol provides straightforward access to indoles bearing an all‐carbon quaternary center at the C3‐position.Xiao-Hui Yang was nominated to be part of this collection by EurJOC Board Member Feng Shi
Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom-economic rhodium and thiophenol co-catalyzed hydroheteroarylation of styrenes with heteroarenes is reported. Alkylated unprotected heteroarenes are accessed under low catalyst loading. This protocol provides straightforward access to indoles bearing an all-carbon quaternary center at the C3-position.
Author Wang, Yi-Xin
Wang, Zhen
Yang, Xiao-Hui
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Issue 34
Keywords ACID
1,3-DIENES
UNACTIVATED ALKENES
FUNCTIONALIZATION
heteroarenes
indoles
CONSTRUCTION
hydroheteroarylation
styrenes
INDOLE ALKALOIDS
FRIEDEL-CRAFTS ALKYLATION
HYDROCARBOFUNCTIONALIZATION
DERIVATIVES
HYDROARYLATION
rhodium
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Snippet Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom-economic rhodium and thiophenol...
Abstract Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom‐economic rhodium and...
Heteroarenes are common moieties in pharmaceuticals and naturally bioactive compounds. In this work, an efficient and atom‐economic rhodium and thiophenol...
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SubjectTerms Alkylation
Carbon
Chemistry
Chemistry, Organic
Indoles
Physical Sciences
Rhodium
Science & Technology
Styrenes
Title Rh-Catalyzed Hydroheteroarylation of Styrenes: Access to Alkylated Heteroarenes with All-Carbon Quaternary Centers
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