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  4. Alcohols in isonitrile-based multicomponent reaction: Passerini reaction of alcohols in the presence of o-iodoxybenzoic acid
 
research article

Alcohols in isonitrile-based multicomponent reaction: Passerini reaction of alcohols in the presence of o-iodoxybenzoic acid

Ngouansavanh, Tifelle
•
Zhu, Jieping  
2006
Angewandte Chemie International Edition

An alc. instead of an aldehyde was found to be an effective reaction partner in the three-component Passerini reaction (P-3CR) in the presence of o-iodoxybenzoic acid (IBX). Thus, by simply heating a soln. of an alc. R1CH2OH [R1 = n-Pr, Ph, PhCH2, AcO(CH2)5, PhCH2OCONHCH2, (R)-AcNHCH(CH2Ph), etc.], a carboxylic acid R2CO2H [R2 = Me, Ph, (S)-MeOCHPh, etc.], an isonitrile R3NC (R3 = Me3C, MeO2CCH2, cyclohexyl, PhCH2), and IBX at 40 DegC, an oxidn./P-3CR sequence occurred smoothly to afford the corresponding alpha -acyloxy carboxamides R2CO2CHR1CONHR3 in good to excellent yields. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1002/anie.200600588
Author(s)
Ngouansavanh, Tifelle
Zhu, Jieping  
Date Issued

2006

Publisher

Wiley-VCH Verlag GmbH

Published in
Angewandte Chemie International Edition
Volume

45

Issue

21

Start page

3495

End page

3497

Subjects

Addition reaction (Passerini; prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid); Amides Role: SPN (Synthetic preparation)

•

PREP (Preparation) (acyloxy; prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid); Condensation reaction (oxidative; prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid); Carboxylic acids; Isocyanides Role: RCT (Reactant)

•

RACT (Reactant or reagent) (prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid); Alcohols Role: RCT (Reactant)

•

RACT (Reactant or reagent) (primary; prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid); Coupling reaction (three-component; prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid)

•

isonitrile oxidative multicomponent Passerini alc carboxylic iodoxybenzoic acid; amide acyloxy prepn

Note

CAN 145:166655

21-2

General Organic Chemistry

Institut de Chimie des Substances Naturelles,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

60-12-8 (2-Phenylethanol); 65-85-0 (Benzoic acid); 71-36-3 (1-Butanol); 100-51-6 (Benzyl alcohol); 931-53-3 (Cyclohexyl isonitrile); 1138-80-3; 1161-13-3; 3966-32-3; 7188-38-7 (tert-Butyl isonitrile); 10340-91-7 (Benzyl isonitrile); 17996-12-2; 26164-26-1; 39687-95-1 (Methyl isocyanoacetate); 52485-50-4; 52485-51-5; 55036-19-6; 68750-24-3 (6-Acetoxy-1-hexanol); 77987-49-6 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid); 64297-64-9 (o-Iodoxybenzoic acid) Role: RGT (Reagent), RACT (Reactant or reagent) (prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid); 89881-22-1P; 132505-08-9P; 237057-79-3P; 901765-08-0P; 901765-09-1P; 901765-10-4P; 901765-11-5P; 901765-12-6P; 901765-13-7P; 901765-14-8P; 901765-15-9P; 901765-16-0P; 901765-17-1P; 901765-18-2P; 901765-19-3P; 901765-20-6P; 901765-21-7P; 901765-22-8P; 901765-23-9P; 901765-24-0P; 901765-25-1P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of alpha -acyloxy amides by three-component Passerini reaction of alcs. with isonitriles and carboxylic acids in the presence of iodoxybenzoic acid)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58442
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