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  4. Synthesis of Chiral Vicinal Diamines by Highly Diastereoselective Three-Component Phenolic Mannich Reaction: Temperature-Dependent Stereodivergency
 
research article

Synthesis of Chiral Vicinal Diamines by Highly Diastereoselective Three-Component Phenolic Mannich Reaction: Temperature-Dependent Stereodivergency

Rondot, Christophe
•
Zhu, Jieping  
2005
Organic Letters

A diastereoselective three-component synthesis of chiral 2-(1,2-diaminoalkyl)phenols from an electron-rich phenol, an amine, and a chiral alpha -N,N-dibenzylamino aldehyde is developed. The diastereoselectivity of this phenolic Mannich reaction is temp.-dependent,and either anti or syn diastereomer can be prepd. by controlling the reaction conditions. Low reaction temp. (-20 DegC) favors the formation of anti adduct, whereas higher temp. (60 DegC) under otherwise identical conditions produces mainly the syn isomer. [on SciFinder (R)]

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Type
research article
DOI
10.1021/ol050334z
Author(s)
Rondot, Christophe
Zhu, Jieping  
Date Issued

2005

Published in
Organic Letters
Volume

7

Issue

8

Start page

1641

End page

1644

Subjects

Amines Role: SPN (Synthetic preparation)

•

PREP (Preparation) (diamines; temp.-dependent stereodivergency in the synthesis of chiral vicinal diamines by a three-component phenolic Mannich reaction); Asymmetric synthesis and induction; Mannich reaction; Temperature (temp.-dependent stereodivergency in the synthesis of chiral vicinal diamines by a three-component phenolic Mannich reaction); Aldehydes; Amines; Phenols Role: RCT (Reactant)

•

RACT (Reactant or reagent) (temp.-dependent stereodivergency in the synthesis of chiral vicinal diamines by a three-component phenolic Mannich reaction)

•

stereoselective Mannich phenol amine amino aldehyde temp

Note

CAN 142:446959

25-10

Benzene, Its Derivatives, and Condensed Benzenoid Compounds

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

Journal

written in English.

54761-04-5 (Ytterbium(III) triflate) Role: CAT (Catalyst use), USES (Uses) (temp.-dependent stereodivergency in the synthesis of chiral vicinal diamines by a three-component phenolic Mannich reaction); 84-85-5 (4-Methoxy-1-naphthol); 90-15-3 (1-Naphthol); 100-46-9 (Benzylamine); 104-94-9 (p-Anisidine); 135-19-3 (2-Naphthol); 533-31-3 (Sesamol); 2393-23-9 (4-Methoxybenzylamine); 3966-32-3; 26164-26-1 ((S)-alpha -Methoxyphenyl acetic acid); 101711-55-1 (2-tert-Butyldimethylsilyloxyethylamine); 111060-63-0 (L-N,N-Dibenzylalaninal); 111060-64-1 (L-N,N-Dibenzylphenylalaninal); 125654-82-2 Role: RCT (Reactant), RACT (Reactant or reagent) (temp.-dependent stereodivergency in the synthesis of chiral vicinal diamines by a three-component phenolic Mannich reaction); 851314-64-2P; 851314-73-3P; 851314-74-4P; 851314-75-5P; 851314-78-8P; 851314-79-9P; 867339-07-9P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (temp.-dependent stereodivergency in the synthesis of chiral vicinal diamines by a three-component phenolic Mannich reaction); 851314-65-3P; 851314-66-4P; 851314-67-5P; 851314-68-6P; 851314-69-7P; 851314-70-0P; 851314-71-1P; 851314-72-2P; 851314-76-6P; 851314-77-7P; 851314-80-2P; 851314-81-3P; 851314-82-4P Role: SPN (Synthetic preparation), PREP (Preparation) (temp.-dependent stereodivergency in the synthesis of chiral vicinal diamines by a three-component phenolic Mannich reaction)

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/20.500.14299/58460
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