Three-component Ugi-Smiles couplings of cyclic imines

Laurent El Kaïm; Laurence Grimaud; Julie Oble; Simon Wagschal

doi:10.1016/j.tetlet.2009.01.145

Three-component Ugi-Smiles couplings of cyclic imines

Laurent El Kaïm
, Laurence Grimaud
, Julie Oble
, Simon Wagschal

Unité Chimie et Procédés

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

Résumé

Cyclic imines react with isocyanides and electron-deficient phenols to afford N-aryl piperidines and pyrrolidines in good yields (Ugi-Smiles couplings of cyclic imines). The starting imines were formed by oxidation with N-chlorosuccinimide followed by a base-induced dehydrochlorination.

langue originale	Anglais
Pages (de - à)	1741-1743
Nombre de pages	3
journal	Tetrahedron Letters
Volume	50
Numéro de publication	15
Les DOIs	https://doi.org/10.1016/j.tetlet.2009.01.145
état	Publié - 15 avr. 2009
Modification externe	Oui

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10.1016/j.tetlet.2009.01.145

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title = "Three-component Ugi-Smiles couplings of cyclic imines",

abstract = "Cyclic imines react with isocyanides and electron-deficient phenols to afford N-aryl piperidines and pyrrolidines in good yields (Ugi-Smiles couplings of cyclic imines). The starting imines were formed by oxidation with N-chlorosuccinimide followed by a base-induced dehydrochlorination.",

author = "Ka{\"i}m, \{Laurent El\} and Laurence Grimaud and Julie Oble and Simon Wagschal",

year = "2009",

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day = "15",

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T1 - Three-component Ugi-Smiles couplings of cyclic imines

AU - Kaïm, Laurent El

AU - Grimaud, Laurence

AU - Oble, Julie

AU - Wagschal, Simon

PY - 2009/4/15

Y1 - 2009/4/15

N2 - Cyclic imines react with isocyanides and electron-deficient phenols to afford N-aryl piperidines and pyrrolidines in good yields (Ugi-Smiles couplings of cyclic imines). The starting imines were formed by oxidation with N-chlorosuccinimide followed by a base-induced dehydrochlorination.

AB - Cyclic imines react with isocyanides and electron-deficient phenols to afford N-aryl piperidines and pyrrolidines in good yields (Ugi-Smiles couplings of cyclic imines). The starting imines were formed by oxidation with N-chlorosuccinimide followed by a base-induced dehydrochlorination.

UR - https://www.scopus.com/pages/publications/60649095384

U2 - 10.1016/j.tetlet.2009.01.145

DO - 10.1016/j.tetlet.2009.01.145

M3 - Article

AN - SCOPUS:60649095384

SN - 0040-4039

VL - 50

SP - 1741

EP - 1743

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 15

ER -

Three-component Ugi-Smiles couplings of cyclic imines

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