Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives

The carbonylation of ArLi (Ar = Ph, o-anisyl) in the presence of alkyl bromides affords diarylalkylcarbinols in good yields. The reaction may be used to obtain alcohols functionalized in the alkyl chain; it can also be adapted to afford substituted tetrahydrofurans. © 1981, American Chemical Society...

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Publicado: 1981
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v46_n22_p4625_Nudelman
http://hdl.handle.net/20.500.12110/paper_00223263_v46_n22_p4625_Nudelman
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id paper:paper_00223263_v46_n22_p4625_Nudelman
record_format dspace
spelling paper:paper_00223263_v46_n22_p4625_Nudelman2023-06-08T14:49:25Z Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives The carbonylation of ArLi (Ar = Ph, o-anisyl) in the presence of alkyl bromides affords diarylalkylcarbinols in good yields. The reaction may be used to obtain alcohols functionalized in the alkyl chain; it can also be adapted to afford substituted tetrahydrofurans. © 1981, American Chemical Society. All rights reserved. 1981 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v46_n22_p4625_Nudelman http://hdl.handle.net/20.500.12110/paper_00223263_v46_n22_p4625_Nudelman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description The carbonylation of ArLi (Ar = Ph, o-anisyl) in the presence of alkyl bromides affords diarylalkylcarbinols in good yields. The reaction may be used to obtain alcohols functionalized in the alkyl chain; it can also be adapted to afford substituted tetrahydrofurans. © 1981, American Chemical Society. All rights reserved.
title Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
spellingShingle Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
title_short Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
title_full Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
title_fullStr Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
title_full_unstemmed Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
title_sort carbonylation of aryllithium reagents in the presence of alkyl halides: one-pot synthesis of diarylalkylcarbinols and derivatives
publishDate 1981
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v46_n22_p4625_Nudelman
http://hdl.handle.net/20.500.12110/paper_00223263_v46_n22_p4625_Nudelman
_version_ 1768543406827503616

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