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Iron‐Catalyzed Synthesis of Amines and Thioethers Directly from Allylic Alcohols

A straightforward and efficient approach for the synthesis of allylic amines and thioethers has been developed by an iron‐catalyzed cross‐coupling reaction using diphosphite ligand. The reaction between allylic alcohols and amines/thiols gave allylic amine and thioester. The method is compatible wit...

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Published in:Asian journal of organic chemistry 2018-05, Vol.7 (5), p.875-878
Main Authors: Wang, Dan‐Yang, Peng, Xiao‐Min, Wang, Guang‐Zhu, Zhang, Ya‐Juan, Guo, Tao, Zhang, Pan‐Ke
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description A straightforward and efficient approach for the synthesis of allylic amines and thioethers has been developed by an iron‐catalyzed cross‐coupling reaction using diphosphite ligand. The reaction between allylic alcohols and amines/thiols gave allylic amine and thioester. The method is compatible with various functional groups, affording products with high yield and monoallylation selectivity. Proceed with an iron fist! A straightforward and efficient approach for the synthesis of allylic amines and thioethers has been developed by an iron‐catalyzed cross‐coupling reaction using a diphosphite ligand. The method is compatible with various functional groups, affording products with high yield and monoallylation selectivity.
doi_str_mv 10.1002/ajoc.201800083
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subjects Alcohol
Alcohols
allylic alcohols
Amines
Chemical synthesis
diphosphite ligands
Functional groups
Iron
Organic chemistry
thioethers
Thiols
title Iron‐Catalyzed Synthesis of Amines and Thioethers Directly from Allylic Alcohols
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