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  4. Catalytic Asymmetric Passerini-Type Reaction: Chiral Aluminum-Organophosphate-Catalyzed Enantioselective alpha -Addition of Isocyanides to Aldehydes
 
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research article

Catalytic Asymmetric Passerini-Type Reaction: Chiral Aluminum-Organophosphate-Catalyzed Enantioselective alpha -Addition of Isocyanides to Aldehydes

Yue, Tao
•
Wang, Mei-Xiang
•
Wang, De-Xian
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2009
The Journal of Organic Chemistry

A chiral Lewis acid catalyst was prepd. by mixing 2 equiv of chiral binol-derived organophosphoric acid and 1 equiv of Et2AlCl. In the presence of a catalytic amt. of [I]2Al(III)Cl complex (0.05 equiv), reaction between alpha -isocyanoacetamides and aldehydes afforded the corresponding 5-aminooxazoles, e.g. II, in good yields and enantioselectivities. Complex [I]2Al(III)Cl isolated as a white solid displayed similar reactivity as that prepd. in situ. [on SciFinder (R)]

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Type
research article
DOI
10.1021/jo9017765
Author(s)
Yue, Tao
•
Wang, Mei-Xiang
•
Wang, De-Xian
•
Masson, Geraldine
•
Zhu, Jieping  
Date Issued

2009

Published in
The Journal of Organic Chemistry
Volume

74

Issue

21

Start page

8396

End page

8399

Subjects

Aldehydes; Isocyanides Role: RCT (Reactant)

•

RACT (Reactant or reagent) (stereoselective prepn. of aminooxazoles via Al-organophosphate-catalyzed asym. Passerini-type reaction of alpha -isocyanatoacetamides and aldehydes); Passerini reaction; Passerini reaction catalysts (stereoselective; stereoselective prepn. of aminooxazoles via Al-organophosphate-catalyzed asym. Passerini-type reaction of alpha -isocyanatoacetamides and aldehydes)

•

organophosphate aluminum catalyst isocyanoacetamide aldehyde asym Passerini type reaction; aminooxazole stereoselective prepn

Note

CAN 151:508512

28-6

Heterocyclic Compounds (More Than One Hetero Atom)

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry,Chinese Academy of Sciences,Beijing,Peop. Rep. China.

Journal

written in English.

96-10-6 (Diethylaluminum chloride); 922711-71-5 Role: CAT (Catalyst use), USES (Uses) (stereoselective prepn. of aminooxazoles via Al-organophosphate-catalyzed asym. Passerini-type reaction of alpha -isocyanatoacetamides and aldehydes); 1192888-03-1P Role: CAT (Catalyst use), SPN (Synthetic preparation), PREP (Preparation), USES (Uses) (stereoselective prepn. of aminooxazoles via Al-organophosphate-catalyzed asym. Passerini-type reaction of alpha -isocyanatoacetamides and aldehydes); 78-84-2 (Isobutanal); 111-71-7 (Heptanal); 122-78-1 (Phenylacetaldehyde); 123-38-6 (Propanal); 85059-38-7; 85059-48-9; 215648-69-4; 336105-88-5; 911817-35-1; 943030-28-2 Role: RCT (Reactant), RACT (Reactant or reagent) (stereoselective prepn. of aminooxazoles via Al-organophosphate-catalyzed asym. Passerini-type reaction of alpha -isocyanatoacetamides and aldehydes); 951241-53-5P; 951241-54-6P; 951241-55-7P; 1192583-11-1P; 1192583-12-2P; 1192583-13-3P; 1192583-14-4P; 1192583-15-5P; 1192583-16-6P; 1192583-17-7P; 1192583-18-8P; 1192583-19-9P Role: SPN (Synthetic preparation), PREP (Preparation) (stereoselective prepn. of aminooxazoles via Al-organophosphate-catalyzed asym. Passerini-type reaction of alpha -isocyanatoacetamides and aldehydes)

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/20.500.14299/58388
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